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Публикации сотрудников

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Публикации за 2018 год

 

 

Egorova, K.S., Ananikov, V.P.

Fundamental importance of ionic interactions in the liquid phase: A review of recent studies of ionic liquids in biomedical and pharmaceutical applications

(2018) Journal of Molecular Liquids, 272, pp. 271-300.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053782252&doi=10.1016%2fj.molliq.2018.09.025&partnerID=40&md5=c801e431db7f8748bb3fc17ed331d0ff

 

DOI: 10.1016/j.molliq.2018.09.025


Panferova, L.I., Chernov, G.N., Levin, V.V., Kokorekin, V.A., Dilman, A.D.

Photoredox mediated annelation of iododifluoromethylated alcohols with 1,1-diarylethylenes

(2018) Tetrahedron, 74 (50), pp. 7136-7142.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055910474&doi=10.1016%2fj.tet.2018.10.062&partnerID=40&md5=597d5f0b747a65544d3c4b2b2d26a850

 

DOI: 10.1016/j.tet.2018.10.062


 

 

Savidov, N., Gloriozova, T.A., Poroikov, V.V., Dembitsky, V.M.

Highly oxygenated isoprenoid lipids derived from fungi and fungal endophytes: Origin and biological activities

(2018) Steroids, 140, pp. 114-124.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054872120&doi=10.1016%2fj.steroids.2018.10.006&partnerID=40&md5=90266acdb7c43218f41b51b4732b8bfc

 

DOI: 10.1016/j.steroids.2018.10.006


 

 

Nagornaya, M.O., Orlova, A.V., Stepanova, E.V., Zinin, A.I., Laptinskaya, T.V., Kononov, L.O.

The use of the novel glycosyl acceptor and supramer analysis in the synthesis of sialyl-α(2–3)-galactose building block

(2018) Carbohydrate Research, 470, pp. 27-35.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055097731&doi=10.1016%2fj.carres.2018.10.001&partnerID=40&md5=80bae6429eb727a2ba150e56a2f1bacc

 

DOI: 10.1016/j.carres.2018.10.001


 

 

Jaquish, R., Reilly, A.K., Lawson, B.P., Golikova, E., Sulman, A.M., Stein, B.D., Lakina, N.V., Tkachenko, O.P., Sulman, E.M., Matveeva, V.G., Bronstein, L.M.

Immobilized glucose oxidase on magnetic silica and alumina: Beyond magnetic separation

(2018) International Journal of Biological Macromolecules, 120, pp. 896-905.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052742134&doi=10.1016%2fj.ijbiomac.2018.08.097&partnerID=40&md5=0aa28eee801334629a9e103a6a3900e9

 

DOI: 10.1016/j.ijbiomac.2018.08.097


 

 

Anikin, O.V., Klenov, M.S., Churakov, A.M., Guskov, A.A., Strelenko, Y.A., Lyssenko, K.A., Tartakovsky, V.A.

Intramolecular Reaction of tert-Butyl-NNO-Azoxy and Cyano Groups – Novel Synthesis of Pyridazine, 1,2,3-Triazepine, and Furan Rings

(2018) European Journal of Organic Chemistry, 2018 (43), pp. 5947-5953.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055875452&doi=10.1002%2fejoc.201800947&partnerID=40&md5=ef54e4665b375c4a7a640d0d8772ed1b

 

DOI: 10.1002/ejoc.201800947


 

 

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Nifantiev, N.E., Usov, A.I.

Fucosylated chondroitin sulfates from the sea cucumbers Holothuria tubulosa and Holothuria stellati

(2018) Carbohydrate Polymers, 200, pp. 1-5.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050464248&doi=10.1016%2fj.carbpol.2018.07.035&partnerID=40&md5=098fbbee36e7215a8eb9707bb9089fcf

 

DOI: 10.1016/j.carbpol.2018.07.035


 

 

Chmovzh, T.N., Knyazeva, E.A., Mikhalchenko, L.V., Golovanov, I.S., Amelichev, S.A., Rakitin, O.A.

Synthesis of the 4,7-Dibromo Derivative of Highly Electron-Deficient [1,2,5]Thiadiazolo[3,4-d]pyridazine and Its Cross-Coupling Reactions

(2018) European Journal of Organic Chemistry, 2018 (41), pp. 5668-5677. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053756200&doi=10.1002%2fejoc.201800961&partnerID=40&md5=fc78a286e0bae329c0bbca0c8d5dcc8e

 

DOI: 10.1002/ejoc.201800961


 

 

Komarova, B.S., Wong, S.S.W., Orekhova, M.V., Tsvetkov, Y.E., Krylov, V.B., Beauvais, A., Bouchara, J.-P., Kearney, J.F., Aimanianda, V., Latgé, J.-P., Nifantiev, N.E.

Chemical Synthesis and Application of Biotinylated Oligo-α-(1 → 3)- d -Glucosides to Study the Antibody and Cytokine Response against the Cell Wall α-(1 → 3)- d -Glucan of Aspergillus fumigatus

(2018) Journal of Organic Chemistry, 83 (21), pp. 12965-12976.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055130242&doi=10.1021%2facs.joc.8b01142&partnerID=40&md5=68daf40a919ddc2f01516275efcb78ee

 

DOI: 10.1021/acs.joc.8b01142


 

 

Vil, V.A., Gomes, G.D.P., Ekimova, M.V., Lyssenko, K.A., Syroeshkin, M.A., Nikishin, G.I., Alabugin, I.V., Terent'Ev, A.O.

Five Roads That Converge at the Cyclic Peroxy-Criegee Intermediates: BF3-Catalyzed Synthesis of β-Hydroperoxy-β-peroxylactones

(2018) Journal of Organic Chemistry, 83 (21), pp. 13427-13445.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055708275&doi=10.1021%2facs.joc.8b02218&partnerID=40&md5=b15591a3cfbb3a69ab2163867ca0739f

 

DOI: 10.1021/acs.joc.8b02218


 

 

Vereshchagin, A.N., Karpenko, K.A., Elinson, M.N., Gorbunov, S.V., Gordeeva, A.M., Proshin, P.I., Goloveshkin, A.S., Egorov, M.P.

Stereoselective one-pot synthesis of polycyanosubstituted piperidines

(2018) Monatshefte fur Chemie, 149 (11), pp. 1979-1989. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053415288&doi=10.1007%2fs00706-018-2187-x&partnerID=40&md5=5fd7adfe184e2e0906a5b1cb75d3fc5b

 

DOI: 10.1007/s00706-018-2187-x


 

 

Belov, N., Nikiforov, R., Polunin, E., Pogodina, Y., Zavarzin, I., Shantarovich, V., Yampolskii, Y.

Gas permeation, diffusion, sorption and free volume of poly(2-trifluoromethyl-2-pentafluoroethyl-1,3-perfluorodioxole)

(2018) Journal of Membrane Science, 565, pp. 112-118.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051765372&doi=10.1016%2fj.memsci.2018.07.077&partnerID=40&md5=c582104bf65e63699981b4686610528a

 

DOI: 10.1016/j.memsci.2018.07.077


 

 

Mukhametshin, T.I., Sharipov, R.I., Petrov, V.A., Kostochko, A.V., Vinogradov, D.B., Bulatov, P.V.

Energy-Intensive Random Block Copolymers of 3,3-Bis (Nitratomethyl) Oxetane and 3-Azidomethyl-3- Methyloxetane

(2018) Propellants, Explosives, Pyrotechnics, 43 (11), pp. 1115-1121.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054666714&doi=10.1002%2fprep.201800216&partnerID=40&md5=cf18844d5e81d2a368cd57415f7f4eff

 

DOI: 10.1002/prep.201800216


 

 

Golovchenko, V.V., Khramova, D.S., Shinen, N., Jamsranjav, G., Chizhov, A.O., Shashkov, A.S.

Structure characterization of the mannofucogalactan isolated from fruit bodies of Quinine conk Fomitopsis officinalis

(2018) Carbohydrate Polymers, 199, pp. 161-169.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049743457&doi=10.1016%2fj.carbpol.2018.06.103&partnerID=40&md5=c2f4928ba21124d7ea5d8b4874f8dbdf

 

DOI: 10.1016/j.carbpol.2018.06.103


 

 

Bilan, M.I., Ustyuzhanina, N.E., Shashkov, A.S., Thanh, T.T.T., Bui, M.L., Tran, T.T.V., Bui, V.N., Nifantiev, N.E., Usov, A.I.

A sulfated galactofucan from the brown alga Hormophysa cuneiformis (Fucales, Sargassaceae)

(2018) Carbohydrate Research, 469, pp. 48-54.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053831304&doi=10.1016%2fj.carres.2018.09.001&partnerID=40&md5=2bb402ce07fab0d2d3fe9f976a3eb3ba

 

DOI: 10.1016/j.carres.2018.09.001


 

 

Petrova, T.E., Boyko, K.M., Nikolaeva, A.Y., Stekhanova, T.N., Gruzdev, E.V., Mardanov, A.V., Stroilov, V.S., Littlechild, J.A., Popov, V.O., Bezsudnova, E.Y.

Structural characterization of geranylgeranyl pyrophosphate synthase GACE1337 from the hyperthermophilic archaeon Geoglobus acetivorans

(2018) Extremophiles, 22 (6), pp. 877-888.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050965367&doi=10.1007%2fs00792-018-1044-5&partnerID=40&md5=e50bf40d48d73778584830cd042ee6d8

 

DOI: 10.1007/s00792-018-1044-5


 

 

Kasimova, A.A., Kenyon, J.J., Arbatsky, N.P., Shashkov, A.S., Popova, A.V., Shneider, M.M., Knirel, Y.A., Hall, R.M.

Acinetobacter baumannii K20 and K21 capsular polysaccharide structures establish roles for UDP-glucose dehydrogenase Ugd2, pyruvyl transferase Ptr2 and two glycosyltransferases

(2018) Glycobiology, 28 (11), pp. 876-884.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055074899&doi=10.1093%2fglycob%2fcwy074&partnerID=40&md5=8bb272484eebfcec0ee973ba26ab68d8

 

DOI: 10.1093/glycob/cwy074


 

 

Ustyuzhanina, N.E., Bilan, M.I., Panina, E.G., Sanamyan, N.P., Dmitrenok, A.S., Tsvetkova, E.A., Ushakova, N.A., Shashkov, A.S., Nifantiev, N.E., Usov, A.I.

Structure and anti-inflammatory activity of a new unusual fucosylated chondroitin sulfate from Cucumaria djakonovi

(2018) Marine Drugs, 16 (10), статья № md16100389, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055078262&doi=10.3390%2fmd16100389&partnerID=40&md5=abb6a8d4c102797535d10e80b7f6f406

 

DOI: 10.3390/md16100389


 

 

Isaev, A.N.

Ammonia and phosphine complexes with proton donors. Hydrogen bonding from the backside of the N(P) lone pair

(2018) Computational and Theoretical Chemistry, 1142, pp. 28-38.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052952764&doi=10.1016%2fj.comptc.2018.08.021&partnerID=40&md5=a4446a62a6b16e5bd62af6ddf30f52a5

 

DOI: 10.1016/j.comptc.2018.08.021


 

 

Zdorovenko, E.L., Besarab, N.V., Shashkov, A.S., Novik, G.I., Shirokov, A.A., Burov, A.M., Knirel, Y.A.

Investigation of O-polysaccharides from bacterial strains of Pseudomonas genus as potential receptors of bacteriophage BIM BV-45

(2018) International Journal of Biological Macromolecules, 118, pp. 1065-1072.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049449935&doi=10.1016%2fj.ijbiomac.2018.06.165&partnerID=40&md5=7404a8b3ffe4d14c71386c63ce8060f8

 

DOI: 10.1016/j.ijbiomac.2018.06.165


 

 

Zabłotni, A., Arbatsky, N.P., Drzewiecka, D., Shashkov, A.S., Knirel, Y.A.

Chemical characterization and serological properties of a unique O-polysaccharide of the Proteus mirabilis Sm 99 clinical strain – Identification of a new, O81, serotype

(2018) International Journal of Biological Macromolecules, 118, pp. 1131-1135.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049602242&doi=10.1016%2fj.ijbiomac.2018.06.174&partnerID=40&md5=27a1c885152be00dc486a37ab9a6e273

 

DOI: 10.1016/j.ijbiomac.2018.06.174


 

 

Chmovzh, T.N., Knyazeva, E.A., Lyssenko, K.A., Popov, V.V., Rakitin, O.A.

Safe synthesis of 4,7-dibromo[1,2,5]thiadiazolo [3,4-d]pyridazine and its SNAr reactions

(2018) Molecules, 23 (10), .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054885507&doi=10.3390%2fmolecules23102576&partnerID=40&md5=bbc4287b56fa81bca2cca6555db9c2c3

 

DOI: 10.3390/molecules23102576


 

 

Abronina, P.I., Malysheva, N.N., Litvinenko, V.V., Zinin, A.I., Kolotyrkina, N.G., Kononov, L.O.

A Ring Contraction of 2,3-Di- O-Silylated Thiopyranosides to Give Thiofuranosides under Mildly Acidic Conditions

(2018) Organic Letters, 20 (19), pp. 6051-6054. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053638427&doi=10.1021%2facs.orglett.8b02424&partnerID=40&md5=6071621e65de421b7d2e925f06764e2a

 

DOI: 10.1021/acs.orglett.8b02424


 

 

Lvov, A.G., Alexeeva, A.M., Lvova, E.A., Krayushkin, M.M., Shirinian, V.Z.

Spectral properties and structure of unsymmetrical diarylethenes based on thiazole ring with hydrogen at the reactive carbon

(2018) Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 203, pp. 348-356.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048014612&doi=10.1016%2fj.saa.2018.05.097&partnerID=40&md5=b1512c652c0fa0cc87cbf6fe45b0798a

 

DOI: 10.1016/j.saa.2018.05.097


 

 

Dmitriev, I.A., Supranovich, V.I., Levin, V.V., Struchkova, M.I., Dilman, A.D.

Visible Light Promoted 2-Bromotetrafluoroethylation of Nitrones

(2018) Advanced Synthesis and Catalysis, 360 (19), pp. 3788-3792.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053231661&doi=10.1002%2fadsc.201800802&partnerID=40&md5=a2f468162162fc181e021ed7478ac49f

 

DOI: 10.1002/adsc.201800802


 

 

Tabolin, A.A., Sukhorukov, A.Y., Ioffe, S.L.

α-Electrophilic Reactivity of Nitronates

(2018) Chemical Record, 18 (10), pp. 1489-1500. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045732465&doi=10.1002%2ftcr.201800009&partnerID=40&md5=863c7538bc16d2e40f1febb84c9123be

 

DOI: 10.1002/tcr.201800009


 

 

Ivanov, S.M., Shestopalov, A.M.

Interaction of Fused 1,2,4-Triazinone with Diborane/Oxidation: A New Route for the Synthesis of Partially Saturated and Aromatic Pyrazolo[5,1-c][1,2,4]triazines

(2018) Journal of Heterocyclic Chemistry, 55 (10), pp. 2427-2433.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052540730&doi=10.1002%2fjhet.3275&partnerID=40&md5=9f82d6452fc868218e440feb17a91658

 

DOI: 10.1002/jhet.3275


 

 

Kirichenko, O., Kapustin, G., Nissenbaum, V., Strelkova, A., Shuvalova, E., Shesterkina, A., Kustov, L.

Thermal decomposition and reducibility of silica-supported precursors of Cu, Fe and Cu–Fe nanoparticles

(2018) Journal of Thermal Analysis and Calorimetry, 134 (1), pp. 233-251.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053224239&doi=10.1007%2fs10973-018-7122-1&partnerID=40&md5=d9089a8a35b7056fada7b9e3af3173ca

 

DOI: 10.1007/s10973-018-7122-1


 

 

Mashkovsky, I.S., Markov, P.V., Bragina, G.O., Baeva, G.N., Rassolov, A.V., Yakushev, I.A., Vargaftik, M.N., Stakheev, A.Y.

Highly-ordered pdin intermetallic nanostructures obtained from heterobimetallic acetate complex: Formation and catalytic properties in diphenylacetylene hydrogenation

(2018) Nanomaterials, 8 (10), статья № 769, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054524376&doi=10.3390%2fnano8100769&partnerID=40&md5=64703b3c4fe14bc5a8323211ed8f1e3d

 

DOI: 10.3390/nano8100769


 

 

Scherbakov, A.M., Zavarzin, I.V., Vorontsova, S.K., Hajra, A., Andreeva, O.E., Yadykov, A.V., Levina, I.S., Volkova, Y.A., Shirinian, V.Z.

Synthesis and evaluation of the antiproliferative activity of benzylidenes of 16-dehydroprogesterone series

(2018) Steroids, 138, pp. 91-101.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050140282&doi=10.1016%2fj.steroids.2018.06.013&partnerID=40&md5=e12e39f009ba65ba29660954a4c68592

 

DOI: 10.1016/j.steroids.2018.06.013


 

 

Farhati, A., Syroeshkin, M., Dammak, M., Jouikov, V.

Covalent grafting of fluoride-encapsulating silsesquioxane F−@Ph8T8 onto glassy carbon

(2018) Electrochemistry Communications, 95, pp. 5-8.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052085714&doi=10.1016%2fj.elecom.2018.08.011&partnerID=40&md5=52b2c07f166a0e63400eba0da8d78a36

 

DOI: 10.1016/j.elecom.2018.08.011


 

 

Arbatsky, N.P., Shneider, M.M., Dmitrenok, A.S., Popova, A.V., Shagin, D.A., Shelenkov, A.A., Mikhailova, Y.V., Edelstein, M.V., Knirel, Y.A.

Structure and gene cluster of the K125 capsular polysaccharide from Acinetobacter baumannii MAR13-1452

(2018) International Journal of Biological Macromolecules, 117, pp. 1195-1199.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048310325&doi=10.1016%2fj.ijbiomac.2018.06.029&partnerID=40&md5=a6c174a9bd40d856019d2ee0b39a4500

 

DOI: 10.1016/j.ijbiomac.2018.06.029


 

 

Lukin, A., Kramer, J., Hartmann, M., Weizel, L., Hernandez-Olmos, V., Falahati, K., Burghardt, I., Kalinchenkova, N., Bagnyukova, D., Zhurilo, N., Rautio, J., Forsberg, M., Ihalainen, J., Auriola, S., Leppänen, J., Konstantinov, I., Pogoryelov, D., Proschak, E., Dar'in, D., Krasavin, M.

Discovery of polar spirocyclic orally bioavailable urea inhibitors of soluble epoxide hydrolase

(2018) Bioorganic Chemistry, 80, pp. 655-667. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050458242&doi=10.1016%2fj.bioorg.2018.07.014&partnerID=40&md5=a7cc930ecff51b508318b7ae655af8f7

 

DOI: 10.1016/j.bioorg.2018.07.014


 

 

Shashkov, A.S., Kenyon, J.J., Arbatsky, N.P., Shneider, M.M., Popova, A.V., Knirel, Y.A., Hall, R.M.

Genetics of biosynthesis and structure of the K53 capsular polysaccharide of acinetobacter baumannii D23 made up of a disaccharide K unit

(2018) Microbiology (United Kingdom), 164 (10), статья № 000710, pp. 1289-1292.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055042182&doi=10.1099%2fmic.0.000710&partnerID=40&md5=9db8c1713627884373134717aab362c5

 

DOI: 10.1099/mic.0.000710


 

 

Salikov, R.F., Trainov, K.P., Platonov, D.N., Belyy, A.Y., Tomilov, Y.V.

Synthesis of 1,2,3,4,5-Penta(methoxycarbonyl)cyclopentadienides through Electrocyclic Ring Closure and Ring Contraction Reactions

(2018) European Journal of Organic Chemistry, 2018 (36), pp. 5065-5068. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052520579&doi=10.1002%2fejoc.201800732&partnerID=40&md5=74037cd8a1dc60c19473340fae09bf50

 

DOI: 10.1002/ejoc.201800732


 

 

Voronin, V.V., Ledovskaya, M.S., Bogachenkov, A.S., Rodygin, K.S., Ananikov, V.P.

Acetylene in organic synthesis: recent progress and new uses

(2018) Molecules, 23 (10), статья № 2442, . Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053827056&doi=10.3390%2fmolecules23102442&partnerID=40&md5=e3f5b9b870c07c5b1e0afe81ef8e0ff5

 

DOI: 10.3390/molecules23102442


 

 

Kokuev, A.O., Antonova, Y.A., Dorokhov, V.S., Golovanov, I.S., Nelyubina, Y.V., Tabolin, A.A., Sukhorukov, A.Y., Ioffe, S.L.

Acylation of Nitronates: [3,3]-Sigmatropic Rearrangement of in Situ Generated N-Acyloxy, N-oxyenamines

(2018) Journal of Organic Chemistry, 83 (18), pp. 11057-11066.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052302958&doi=10.1021%2facs.joc.8b01652&partnerID=40&md5=ad077ff09e7822cc419b841cd164207d

 

DOI: 10.1021/acs.joc.8b01652


 

 

Mulina, O.M., Ilovaisky, A.I., Terent'ev, A.O.

Oxidative Coupling with S–N Bond Formation

(2018) European Journal of Organic Chemistry, 2018 (34), pp. 4648-4672. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052629864&doi=10.1002%2fejoc.201800838&partnerID=40&md5=f322338948eb9c09dd6e344c65a8dc4b

 

DOI: 10.1002/ejoc.201800838


 

 

Starosotnikov, A.M., Bastrakov, M.A., Kachala, V.V., Fedyanin, I.V., Shevelev, S.A., Dalinger, I.L.

Unusual Pericyclic Reactivity of 4-Nitrobenzofuroxans in 1,3-Dipolar Cycloaddition with N-Benzyl Azomethine Ylide – A New Example of Multiple C–C-Bond Forming Transformations.

(2018) ChemistrySelect, 3 (34), pp. 9773-9777.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053418264&doi=10.1002%2fslct.201802117&partnerID=40&md5=a5b511e445099368968f23b6fa27c6a3

 

DOI: 10.1002/slct.201802117


 

 

Anisimova, N.Y., Ustyuzhanina, N.E., Bilan, M.I., Donenko, F.V., Ushakova, N.A., Usov, A.I., Kiselevskiy, M.V., Nifantiev, N.E.

Influence of modified fucoidan and related sulfated oligosaccharides on hematopoiesis in cyclophosphamide-induced mice

(2018) Marine Drugs, 16 (9), статья № 333, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053838637&doi=10.3390%2fmd16090333&partnerID=40&md5=9ef5b506279cbc0bc527d8366416fe99

 

DOI: 10.3390/md16090333


 

 

Golovanov, I.S., Mazeina, G.S., Nelyubina, Y.V., Novikov, R.A., Mazur, A.S., Britvin, S.N., Tartakovsky, V.A., Ioffe, S.L., Sukhorukov, A.Y.

Exploiting Coupling of Boronic Acids with Triols for a pH-Dependent "click-Declick" Chemistry

(2018) Journal of Organic Chemistry, 83 (17), pp. 9756-9773.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052327261&doi=10.1021%2facs.joc.8b01296&partnerID=40&md5=d27500562c2de52b80d14728dbbab7ee

 

DOI: 10.1021/acs.joc.8b01296


 

 

Motornov, V.A., Tabolin, A.A., Novikov, R.A., Nelyubina, Y.V., Nenajdenko, V.G., Ioffe, S.L.

Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: One-pot three-component assembly of fluorinated bicyclic nitroso acetals

(2018) Organic Chemistry Frontiers, 5 (17), pp. 2593-2599.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051996067&doi=10.1039%2fc8qo00623g&partnerID=40&md5=00743a7f69040c6aab0a89a629cad85b

 

DOI: 10.1039/c8qo00623g


 

 

Kostenko, A.A., Kucherenko, A.S., Zlotin, S.G.

Recyclable C2-symmetric tertiary amine-squaramide organocatalysts: Design and application to asymmetric synthesis of γ-nitrocarbonyl compounds

(2018) Tetrahedron, 74 (36), pp. 4769-4776.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050673972&doi=10.1016%2fj.tet.2018.07.043&partnerID=40&md5=d4fb74ff275237e858110a9e6f6627fa

 

DOI: 10.1016/j.tet.2018.07.043


 

 

Belen'kii, L.I., Radzhabov, M.R., Pivina, T.S.

Quantum-chemical study of the mechanism of aminomethylation of tetrazoles according to the elimination–addition scheme without preliminary formation of N-protonated azolium salts

(2018) Mendeleev Communications, 28 (5), pp. 548-550.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054335300&doi=10.1016%2fj.mencom.2018.09.034&partnerID=40&md5=8fac3da75674da5eb3e002b427cd785b

 

DOI: 10.1016/j.mencom.2018.09.034


 

 

Rassolov, A.V., Baeva, G.N., Mashkovsky, I.S., Stakheev, A.Y.

PdCu/Al2O3 catalyst for Sonogashira cross-coupling: effect of a Pd/Cu ratio on the catalytic performance

(2018) Mendeleev Communications, 28 (5), pp. 538-540.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054307980&doi=10.1016%2fj.mencom.2018.09.030&partnerID=40&md5=6ba93210c3db059956691c44366120d2

 

DOI: 10.1016/j.mencom.2018.09.030


 

 

Panova, M.V., Orlova, A.V., Kononov, L.O.

Stabilization of sialyl cation in axial conformation assisted by remote acyl groups

(2018) Russian Chemical Bulletin, 67 (9), pp. 1573-1579.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056272141&doi=10.1007%2fs11172-018-2260-y&partnerID=40&md5=84fe28abbe8a81971e84f853abcb25d7

 

DOI: 10.1007/s11172-018-2260-y


 

 

Kuznetsov, V.V., Kachala, V.V., Makhova, N.N.

Synthesis of hybrid structures comprising diaziridine and cyclopropane rings in one molecule

(2018) Mendeleev Communications, 28 (5), pp. 497-500.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054329204&doi=10.1016%2fj.mencom.2018.09.015&partnerID=40&md5=6ee1c2842621accae60e155de36e81e7

 

DOI: 10.1016/j.mencom.2018.09.015


 

 

Larin, A., Ovchinnikov, I., Fershtat, L., Makhova, N.

3,30-(Diazene-1,2-diyl)bis[4-(nitroamino)-1,2,5- oxadiazole 2-oxide]

(2018) MolBank, 2018 (3), статья № M1003, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050919764&doi=10.3390%2fM1003&partnerID=40&md5=ff1b769a467e24c44cda35a49b3ce167

 

DOI: 10.3390/M1003


 

 

Lapitskaya, M.A., Vil, V.A., Daeva, E.D., Terent'ev, A.O., Pivnitsky, K.K.

Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity

(2018) Mendeleev Communications, 28 (5), pp. 505-507.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054292530&doi=10.1016%2fj.mencom.2018.09.018&partnerID=40&md5=da9ade9a6047721f7e13a0733cb7df3b

 

DOI: 10.1016/j.mencom.2018.09.018


 

 

Pokhvisneva, G.V., Gordeev, P.B., Nikitin, S.V., Smirnov, G.A., Ternikova, T.V., Luk’yanov, O.A.

3,3-Bis(2-nitroxyethyl) derivatives of 1,1′-[methylenebis(oxy)]bis(triaz-1-ene 2-oxides) as a new type of NO donors

(2018) Russian Chemical Bulletin, 67 (9), pp. 1655-1661. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056239689&doi=10.1007%2fs11172-018-2273-6&partnerID=40&md5=3ef683f7be1530a057337496092e74dc

 

DOI: 10.1007/s11172-018-2273-6


 

 

Lyalin, B.V., Sigacheva, V.L., Fershtat, L.L., Makhova, N.N., Petrosyan, V.A.

Eco-friendly N–N coupling of aminofuroxans into azofuroxans under the action of electrogenerated hypohalites

(2018) Mendeleev Communications, 28 (5), pp. 518-520.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054300826&doi=10.1016%2fj.mencom.2018.09.023&partnerID=40&md5=c376710b28d2001ea65dcfdefca92628

 

DOI: 10.1016/j.mencom.2018.09.023


 

 

Kalenchuk, A.N., Bogdan, V.I., Dunaev, S., Kustov, L.M.

Effect of Isomerization on the Reversible Reaction of Hydrogenation-Dehydrogenation of ortho-Terphenyl on a Pt/C Catalyst

(2018) Chemical Engineering and Technology, 41 (9), pp. 1842-1846.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052115015&doi=10.1002%2fceat.201800312&partnerID=40&md5=398d6ebdac4b691d06374af27352057b

 

DOI: 10.1002/ceat.201800312


 

 

Krasovskiy, V.G., Chernikova, Е.А., Glukhov, L.М., Kаpustin, G.I., Kоroteev, А.А., Kustov, L.М.

Hydroxyl-containing imidazolium ionic liquids

(2018) Russian Chemical Bulletin, 67 (9), pp. 1621-1626.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056264814&doi=10.1007%2fs11172-018-2268-3&partnerID=40&md5=a14227883e3b18eb6facb9b8c2d926a8

 

DOI: 10.1007/s11172-018-2268-3


 

 

Lvov, A.G., Khusniyarov, M.M., Shirinian, V.Z.

Azole-based diarylethenes as the next step towards advanced photochromic materials

(2018) Journal of Photochemistry and Photobiology C: Photochemistry Reviews, 36, pp. 1-23. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047409506&doi=10.1016%2fj.jphotochemrev.2018.04.002&partnerID=40&md5=6d801b1b67cb0a718b46b46f2d6fbfb0

 

DOI: 10.1016/j.jphotochemrev.2018.04.002


 

 

Vereshchagin, A.N., Karpenko, K.A., Elinson, M.N., Goloveshkin, A.S., Ushakov, I.E., Egorov, M.P.

Four-component stereoselective synthesis of tetracyano-substituted piperidines

(2018) Research on Chemical Intermediates, 44 (9), pp. 5623-5634. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046040774&doi=10.1007%2fs11164-018-3444-7&partnerID=40&md5=e3361fa215e4d19a3e6dc21438a8e116

 

DOI: 10.1007/s11164-018-3444-7


 

 

Isaeva, V.I., Nefedov, O.M., Kustov, L.M.

Metal–organic frameworks-based catalysts for biomass processing

(2018) Catalysts, 8 (9), статья № 368, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053759586&doi=10.3390%2fcatal8090368&partnerID=40&md5=2e3a67dd598d93096af01330cb604627

 

DOI: 10.3390/catal8090368


 

 

Elinson, M.N., Vereshchagin, A.N., Anisina, Y.E., Goloveshkin, A.S., Ushakov, I.E., Egorov, M.P.

Multicomponent transformation of salicylaldehydes, 2-aminoprop-1-ene-1,1,3-tricarbonitrile, and pyrazolin-5-ones into substituted 2,4-diamino-5-(5-hydroxy-3-methyl-1H-pyrazol-4-yl)-5H-chromeno[2,3-b]pyridine-3-carbonitriles

(2018) Russian Chemical Bulletin, 67 (9), pp. 1695-1703.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056267776&doi=10.1007%2fs11172-018-2278-1&partnerID=40&md5=8c5054fdf092a389af9956acdf9a9ff1

 

DOI: 10.1007/s11172-018-2278-1


 

 

Smirnov, G.A., Gordeev, P.B., Nikitin, S.V., Pokhvisneva, G.V., Ternikova, T.V., Chistokhvalov, I.M., Luk’yanov, O.A.

Bis-, tris-, and tetrakis-N-(2-nitroxyethyl) derivatives of 1,1’-[methylenebis(oxy)]bis(triaz-1-ene 2-oxides)

(2018) Russian Chemical Bulletin, 67 (9), pp. 1662-1670.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056213327&doi=10.1007%2fs11172-018-2274-5&partnerID=40&md5=b364abc58fa54b2072ef8ecfacee03e1

 

DOI: 10.1007/s11172-018-2274-5


 

 

Kuznetsov, Y.V., Levina, I.S., Scherbakov, A.M., Andreeva, O.E., Dmitrenok, A.S., Malyshev, O.R., Zavarzin, I.V.

3,20-Dihydroxy-13α-19-norpregna-1,3,5(10)-trienes. Synthesis, structures, and cytotoxic, estrogenic, and antiestrogenic effects

(2018) Steroids, 137, pp. 1-13.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050537709&doi=10.1016%2fj.steroids.2018.07.007&partnerID=40&md5=bf71e1ae46eabc38e6d623417a89e314

 

DOI: 10.1016/j.steroids.2018.07.007


 

 

Elinson, M.N., Vereshchagin, A.N., Anisina, Y.E., Fakhrutdinov, A.N., Goloveshkin, A.S., Egorov, M.P.

A facile and efficient multicomponent approach to 5-[5-hydroxy- 3-(trifluoromethyl)-1H-pyrazol-4-yl]-5H-chromeno[2,3-b]pyridines

(2018) Journal of Fluorine Chemistry, 213, pp. 31-36.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049422626&doi=10.1016%2fj.jfluchem.2018.06.008&partnerID=40&md5=c3c3922b16c0ec6852ae4f87cbe61a9e

 

DOI: 10.1016/j.jfluchem.2018.06.008


 

 

Elinson, M.N., Sokolova, O.O., Korshunov, A.D., Barba, F., Batanero, B.

Electrocatalytic Cascade Reaction of Aldehydes and 4-Hydroxy-6-methyl-2H-pyran-2-one

(2018) Electrocatalysis, 9 (5), pp. 602-607.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050411212&doi=10.1007%2fs12678-018-0470-6&partnerID=40&md5=ae20e70a7130e934f09ea831ad64b352

 

DOI: 10.1007/s12678-018-0470-6


 

 

Gromachevskaya, E.V., Kaigorodova, E.А., Konyushkin, L.D., Krapivin, G.D.

Studies on quinazolines 7*. Alkylation of 2-aryl-4,4-diphenyl-3,4-dihydroquinazolines with methyl iodide

(2018) Chemistry of Heterocyclic Compounds, 54 (9), pp. 887-891.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055880306&doi=10.1007%2fs10593-018-2363-2&partnerID=40&md5=04acaa1913156d7d8179dfb56fea74b6

 

DOI: 10.1007/s10593-018-2363-2


 

 

Demin, D.Y., Myannik, K.A., Ermolich, P.A., Krayushkin, M.M., Yarovenko, V.N.

Synthesis of 3-(N-arylthiocarbamoyl)chromones from 2-hydroxyaryl amino enones and isothiocyanates

(2018) Mendeleev Communications, 28 (5), pp. 485-486.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054338843&doi=10.1016%2fj.mencom.2018.09.010&partnerID=40&md5=48ca24f5084e0634999424a101f6b444

 

DOI: 10.1016/j.mencom.2018.09.010


 

 

Lempert, D.B., Kazakov, A.I., Soglasnova, S.I., Dalinger, I.L., Sheremetev, A.B.

Energetic abilities of nitro derivatives of isomeric (pyrazol-3-yl)tetrazoles as components of solid composite propellants

(2018) Russian Chemical Bulletin, 67 (9), pp. 1580-1588.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056260746&doi=10.1007%2fs11172-018-2261-x&partnerID=40&md5=7c2df4a8cd3809bd5a06ce8aee195e18

 

DOI: 10.1007/s11172-018-2261-x


 

 

Kostyukhin, E.M., Kustov, L.M.

Microwave-assisted synthesis of magnetite nanoparticles possessing superior magnetic properties

(2018) Mendeleev Communications, 28 (5), pp. 559-561.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054328283&doi=10.1016%2fj.mencom.2018.09.038&partnerID=40&md5=95cfd996952d72c2abbc2cf0f11d2bf9

 

DOI: 10.1016/j.mencom.2018.09.038


 

 

Tarasov, A.L., Kostyukhin, E.M., Kustova, L.M.

Gasification of metal-containing coals and carbons via their reaction with carbon dioxide

(2018) Mendeleev Communications, 28 (5), pp. 530-532.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054342198&doi=10.1016%2fj.mencom.2018.09.027&partnerID=40&md5=a581f9287f7d6156ef6af2ae9cb4cba6

 

DOI: 10.1016/j.mencom.2018.09.027


 

 

Vil, V.A., Gloriozova, T.A., Poroikov, V.V., Terent’ev, A.O., Savidov, N., Dembitsky, V.M.

Peroxy steroids derived from plant and fungi and their biological activities

(2018) Applied Microbiology and Biotechnology, 102 (18), pp. 7657-7667.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049684286&doi=10.1007%2fs00253-018-9211-2&partnerID=40&md5=715ccdf64020ebb8a6b6181f33e0de68

 

DOI: 10.1007/s00253-018-9211-2


 

 

Borodina, T., Marchenko, I., Trushina, D., Volkova, Y., Shirinian, V., Zavarzin, I., Kondrakhin, E., Kovalev, G., Kovalchuk, M., Bukreeva, T.

A novel formulation of zolpidem for direct nose-to-brain delivery: synthesis, encapsulation and intranasal administration to mice

(2018) Journal of Pharmacy and Pharmacology, 70 (9), pp. 1164-1173.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051105425&doi=10.1111%2fjphp.12958&partnerID=40&md5=4241a604058d03721ff9cac87793c1cd

 

DOI: 10.1111/jphp.12958


 

 

Roitershtein, D.M., Puntus, L.N., Vinogradov, A.A., Lyssenko, K.A., Minyaev, M.E., Dobrokhodov, M.D., Taidakov, I.V., Varaksina, E.A., Churakov, A.V., Nifant'Ev, I.E.

Polyphenylcyclopentadienyl Ligands as an Effective Light-Harvesting μ-Bonded Antenna for Lanthanide +3 Ions

(2018) Inorganic Chemistry, 57 (16), pp. 10199-10213. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051866541&doi=10.1021%2facs.inorgchem.8b01405&partnerID=40&md5=0a1f51c98f939370d295bb58b0ee00be

 

DOI: 10.1021/acs.inorgchem.8b01405


 

 

Bystrov, D.M., Zhilin, E.S., Fershtat, L.L., Romanova, A.A., Ananyev, I.V., Makhova, N.N.

Tandem Condensation/Rearrangement Reaction of 2-Aminohetarene N-Oxides for the Synthesis of Hetaryl Carbamates

(2018) Advanced Synthesis and Catalysis, 360 (16), pp. 3157-3163.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051748748&doi=10.1002%2fadsc.201800407&partnerID=40&md5=39165332e5692b953a351b498e5d9ae4

 

DOI: 10.1002/adsc.201800407


 

 

Krylov, I.B., Paveliev, S.A., Syroeshkin, M.A., Korlyukov, A.A., Dorovatovskii, P.V., Zubavichus, Y.V., Nikishin, G.I., Terent’ev, A.O.

Hypervalent iodine compounds for anti-markovnikov-type iodo-oxyimidation of vinylarenes

(2018) Beilstein Journal of Organic Chemistry, 14, pp. 2146-2155.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052236684&doi=10.3762%2fbjoc.14.188&partnerID=40&md5=f43b0740f15d62358b5cff6b2b69e6ba

 

DOI: 10.3762/bjoc.14.188


 

 

Ogurtsov, V.A., Dorovatovskii, P.V., Zubavichus, Y.V., Khrustalev, V.N., Fakhrutdinov, A.N., Zlotin, S.G., Rakitin, O.A.

[1,2,5]Oxadiazolo[3,4-d]pyridazine 1,5,6-trioxides: efficient synthesis via the reaction of 3,4-bis(hydroxyimino)methyl)-1,2,5-oxadiazole 2-oxides with a mixture of concentrated nitric and trifluoroacetic acids and structural characterization

(2018) Tetrahedron Letters, 59 (32), pp. 3143-3146.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049579854&doi=10.1016%2fj.tetlet.2018.07.015&partnerID=40&md5=86e038279a433ca92fb999a73c071e74

 

DOI: 10.1016/j.tetlet.2018.07.015


 

 

Khotyantseva, E.A., Tabolin, A.A., Novikov, R.A., Nelyubina, Y.V., Ioffe, S.L.

Synthesis of unsaturated silyl nitronates via the silylation of conjugated nitroalkenes

(2018) Tetrahedron Letters, 59 (32), pp. 3128-3131.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049464449&doi=10.1016%2fj.tetlet.2018.07.011&partnerID=40&md5=5859498e66e2c4b249a5298f878e5a35

 

DOI: 10.1016/j.tetlet.2018.07.011


 

 

Novikov, R.A., Borisov, D.D., Tarasova, A.V., Tkachev, Y.V., Tomilov, Y.V.

Three-Component Gallium(III)-Promoted Addition of Halide Anions and Acetylenes to Donor–Acceptor Cyclopropanes

(2018) Angewandte Chemie - International Edition, 57 (32), pp. 10293-10298. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050503423&doi=10.1002%2fanie.201803541&partnerID=40&md5=a6e9505db1f2ee1f939710d3282bc7eb

 

DOI: 10.1002/anie.201803541


 

 

Chagarovskiy, A.O., Vasin, V.S., Kuznetsov, V.V., Ivanova, O.A., Rybakov, V.B., Shumsky, A.N., Makhova, N.N., Trushkov, I.V.

(3+3)-Annulation of Donor–Acceptor Cyclopropanes with Diaziridines

(2018) Angewandte Chemie - International Edition, 57 (32), pp. 10338-10342. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050455655&doi=10.1002%2fanie.201805258&partnerID=40&md5=22f18da02a6fb65d52265bcdbbacfe02

 

DOI: 10.1002/anie.201805258


 

 

Zotova, M.A., Novikov, R.A., Shulishov, E.V., Tomilov, Y.V.

GaCl3-Mediated "inverted" Formal [3 + 2]-Cycloaddition of Donor-Acceptor Cyclopropanes to Allylic Systems

(2018) Journal of Organic Chemistry, 83 (15), pp. 8193-8207. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049412894&doi=10.1021%2facs.joc.8b00959&partnerID=40&md5=bcfbe64144fcba8d649a0fb3133b9979

 

DOI: 10.1021/acs.joc.8b00959


 

 

Novikov, R.A., Borisov, D.D., Zotova, M.A., Denisov, D.A., Tkachev, Y.V., Korolev, V.A., Shulishov, E.V., Tomilov, Y.V.

Cascade Cleavage of Three-Membered Rings in the Reaction of D-A Cyclopropanes with 4,5-Diazaspiro[2.4]hept-4-enes: A Route to Highly Functionalized Pyrazolines

(2018) Journal of Organic Chemistry, 83 (15), pp. 7836-7851. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048371994&doi=10.1021%2facs.joc.8b00725&partnerID=40&md5=43528bc8c7b8b447185cc242407ed271

 

DOI: 10.1021/acs.joc.8b00725


 

 

Panferova, L.I., Struchkova, M.I., Dilman, A.D.

Light-Promoted Allylation of Iododifluoromethylated Alcohols

(2018) European Journal of Organic Chemistry, 2018 (27), pp. 3834-3836. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050391524&doi=10.1002%2fejoc.201800543&partnerID=40&md5=b84e98639e327553c53a248c6afff6ef

 

DOI: 10.1002/ejoc.201800543


 

 

Kalugin, V.E., Shestopalov, A.M.

Synthesis of 5-aminopyrido[3′,2′:4,5]thieno[3,2-c]isoquinoline derivatives from 3-cyanopyridine-2(1H)-thiones and 2-(chloromethyl)benzamide

(2018) Russian Chemical Bulletin, 67 (8), pp. 1492-1499.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055327244&doi=10.1007%2fs11172-018-2245-x&partnerID=40&md5=df4766010d49b5046f0797dce9087ce7

 

DOI: 10.1007/s11172-018-2245-x


 

 

Vereshchagin, A.N., Karpenko, K.A., Elinson, M.N., Gorbunov, S.V., Anisina, Y.E., Egorov, M.P.

Stereoselective multicomponent synthesis of (2RS,6SR)-2,6-diaryl-3,3,5,5-tetracyanopiperidines

(2018) Russian Chemical Bulletin, 67 (8), pp. 1534-1537.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055323706&doi=10.1007%2fs11172-018-2252-y&partnerID=40&md5=e239d3be6ae491c5827b96eae5c7814f

 

DOI: 10.1007/s11172-018-2252-y


 

 

Ivanov, S.M., Shestopalov, A.M.

Interaction of 4-Oxo-4H-pyrazolo[5,1-c][1,2,4]triazin-1-ides with Grignard Reagents

(2018) Journal of Heterocyclic Chemistry, 55 (8), pp. 1966-1972. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050548640&doi=10.1002%2fjhet.3236&partnerID=40&md5=ee0205488327717a41dcfc3d3c9fa670

 

DOI: 10.1002/jhet.3236


 

 

Tarasov, A.L.

The ethanol to acetaldehyde conversion activated by microwave radiation

(2018) Russian Chemical Bulletin, 67 (8), pp. 1390-1393.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055333713&doi=10.1007%2fs11172-018-2229-x&partnerID=40&md5=6f0212748b5acbb955ce38efe304ff8f

 

DOI: 10.1007/s11172-018-2229-x


 

 

Sheveleva, E.E., Pimenov, V.G., Blagodatskikh, I.V., Vyshivannaya, O.V., Abramchuk, S.S., Sakharov, A.M.

Synthesis, structure, and properties of bisphenol A formaldehyde sol—precursor of low-density aerogel

(2018) Colloid and Polymer Science, 296 (8), pp. 1313-1322.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048574542&doi=10.1007%2fs00396-018-4343-6&partnerID=40&md5=353655054b0ab53d5d5bcb6b9396c154

 

DOI: 10.1007/s00396-018-4343-6


 

 

Ivanov, S.M., Mironovich, L.M., Rodinovskaya, L.A., Shestopalov, A.M.

Synthesis of new 4-oxo-7-(1H-1,2,3-triazol-1-yl)-4,6-dihydropyrazolo[5,1-c][1,2,4]triazines

(2018) Russian Chemical Bulletin, 67 (8), pp. 1482-1486.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055311738&doi=10.1007%2fs11172-018-2243-z&partnerID=40&md5=4fdad7e31cce2a3a3c0ff02a74d249f6

 

DOI: 10.1007/s11172-018-2243-z


 

 

Ivanov, S.M., Mironovich, L.M., Rodinovskaya, L.A., Shestopalov, A.M.

Synthesis of new 4-oxo-1,2,3,4-tetrahydropyrazolo[5,1-с][1,2,4]triazines

(2018) Russian Chemical Bulletin, 67 (8), pp. 1487-1491.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055344961&doi=10.1007%2fs11172-018-2244-y&partnerID=40&md5=acac54eda0e36cc225da1b7d4a240f22

 

DOI: 10.1007/s11172-018-2244-y


 

 

Nikitin, S.V., Pokhvisneva, G.V., Ternikova, T.V., Gordeev, P.B., Chistokhvalov, I.M., Smirnov, G.A., Luk’yanov, O.A.

N-β-Nitroxyethyl derivatives of 1,1’-[methylenebis(oxy)]bis(triaz-1-ene 2-oxides)

(2018) Russian Chemical Bulletin, 67 (8), pp. 1445-1451. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055322116&doi=10.1007%2fs11172-018-2238-9&partnerID=40&md5=7de5b2cdcdfb73aa7b03511823d47e06

 

DOI: 10.1007/s11172-018-2238-9


 

 

Aldoshin, A.S., Tabolin, A.A., Ioffe, S.L., Nenajdenko, V.G.

Green, Catalyst-Free Reaction of Indoles with β-Fluoro-β-nitrostyrenes in Water

(2018) European Journal of Organic Chemistry, 2018 (27), pp. 3816-3825. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050389978&doi=10.1002%2fejoc.201800385&partnerID=40&md5=3714c53694548da7ba15187e0a709481

 

DOI: 10.1002/ejoc.201800385


 

 

Vereshchagin, A.N., Elinson, M.N., Anisina, Y.E., Karpenko, K.A., Goloveshkin, A.S., Zlotin, S.G., Egorov, M.P.

High diastereoselective amine-catalyzed Knoevenagel–Michael-cyclization–ring-opening cascade between aldehydes, 3-arylisoxazol-5(4H)-ones and 3-aminocyclohex-2-en-1-ones

(2018) Molecular Diversity, 22 (3), pp. 627-636.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046040505&doi=10.1007%2fs11030-018-9817-4&partnerID=40&md5=3f28150fceade499bd5e2878adff8b53

 

DOI: 10.1007/s11030-018-9817-4


 

 

Kalenchuk, A.N., Koklin, A.E., Bogdan, V.I., Kustov, L.M.

Hydrogenation of naphthalene and anthracene on Pt/C catalysts

(2018) Russian Chemical Bulletin, 67 (8), pp. 1406-1411.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055337211&doi=10.1007%2fs11172-018-2232-2&partnerID=40&md5=390ceeb458fa03e3a975721f193a8e64

 

DOI: 10.1007/s11172-018-2232-2


 

 

Levin, V.V., Agababyan, D.P., Struchkova, M.I., Dilman, A.D.

Dimerization of Benzyl and Allyl Halides via Photoredox-Mediated Disproportionation of Organozinc Reagents

(2018) Synthesis (Germany), 50 (15), статья № ss-2018-c0067-st, pp. 2930-2935.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047297385&doi=10.1055%2fs-0036-1591583&partnerID=40&md5=c05982e65580b7e9f03d09779c7273d3

 

DOI: 10.1055/s-0036-1591583


 

 

Kiseleva, E.P., Mikhailopulo, K.I., Zdorovenko, E.L., Knirel, Y.A., Novik, G.I.

Linear α-(1 → 6)-D-glucan from Bifidobacterium bifidum BIM В-733D is low molecular mass biopolymer with unique immunochemical properties

(2018) Carbohydrate Research, 466, pp. 39-50.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044518019&doi=10.1016%2fj.carres.2017.12.008&partnerID=40&md5=2525a19624f6b209b3ef870f96f35a07

 

DOI: 10.1016/j.carres.2017.12.008


 

 

Shashkov, A.S., Senchenkova, S.N., Naumenko, O.I., Kalinchuk, N.A., Perepelov, A.V., Knirel, Y.A.

Escherichia coli O106, a new member of a group of enteric bacteria sharing an O-polysaccharide backbone structure

(2018) Russian Chemical Bulletin, 67 (8), pp. 1538-1541.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055324492&doi=10.1007%2fs11172-018-2253-x&partnerID=40&md5=f7fa508b3f3ed1c8bf3d26743e3ede35

 

DOI: 10.1007/s11172-018-2253-x


 

 

Gazieva, G.A., Izmest’ev, A.N., Anikina, L.V., Pukhov, S.A., Meshchaneva, M.E., Khakimov, D.V., Kolotyrkina, N.G., Kravchenko, A.N.

The influence of substituents on the reactivity and cytotoxicity of imidazothiazolotriazinones

(2018) Molecular Diversity, 22 (3), pp. 585-599.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85043715307&doi=10.1007%2fs11030-018-9813-8&partnerID=40&md5=b644a22c9b9225bd647610edccbe5e93

 

DOI: 10.1007/s11030-018-9813-8


 

 

Ignatov, A.V., Varakutin, A.E., Solov’eva, I.N., Karmanova, I.B., Kozlov, I.A., Semenova, M.N., Semenov, V.V.

Efficient hydrogenation of benzaldoximes and Schiff bases on ceramic high-porosity palladium catalysts

(2018) Russian Chemical Bulletin, 67 (8), pp. 1394-1400.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055338256&doi=10.1007%2fs11172-018-2230-4&partnerID=40&md5=e5b6edd20cab604c8e2b2d60fb55d806

 

DOI: 10.1007/s11172-018-2230-4


 

 

Zdorovenko, E.L., Shashkov, A.S., Kadykova, A.A., Kiseleva, E.P., Savich, V.V., Novik, G.I., Knirel, Y.A.

Structures of O-specific polysaccharides of Pseudomonas psyhrotolerans BIM B-1158G

(2018) Carbohydrate Research, 465, pp. 35-39.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048712160&doi=10.1016%2fj.carres.2018.06.006&partnerID=40&md5=03539b204eb52de6843dcf5551d6aab5

 

DOI: 10.1016/j.carres.2018.06.006


 

 

Sigida, E.N., Fedonenko, Y.P., Shashkov, A.S., Konnova, S.A., Ignatov, V.V.

Structure of the O-specific polysaccharide from Azospirillum fermentarium CC-LY743T

(2018) Carbohydrate Research, 465, pp. 40-43.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048720064&doi=10.1016%2fj.carres.2018.06.003&partnerID=40&md5=49342b9cdf56815641860e9183acf031

 

DOI: 10.1016/j.carres.2018.06.003


 

 

Naumenko, O.I., Song, J., Senchenkova, S.N., Jiang, X., Perepelov, A.V., Shashkov, A.S., Knirel, Y.A.

Structural studies on the O-polysaccharide of Escherichia coli O57

(2018) Carbohydrate Research, 465, pp. 1-3.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047822711&doi=10.1016%2fj.carres.2018.05.006&partnerID=40&md5=715b3251db9edef63f3caa171b63490a

 

DOI: 10.1016/j.carres.2018.05.006


 

 

Abronina, P.I., Zinin, A.I., Romashin, D.A., Tereshina, V.V., Chizhov, A.O., Kononov, L.O.

Application of a Janus aglycon with dual function in benzyl-free synthesis of spacer-armed oligosaccharide fragments of polysaccharides from rhizobacterium Azospirillum brasilense sp7

(2018) Carbohydrate Research, 464, pp. 28-43. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047238644&doi=10.1016%2fj.carres.2018.05.005&partnerID=40&md5=8eff29196056c1b4c2290997e89f5a07

 

DOI: 10.1016/j.carres.2018.05.005


 

 

Kustov, L.M., Furman, D.B.

Catalytic synthesis of octadiene-1,7 from ethylene and cyclohexene

(2018) Journal of Organometallic Chemistry, 867, pp. 261-265. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041728110&doi=10.1016%2fj.jorganchem.2018.01.059&partnerID=40&md5=6058e0aee659599609f180605ddfb968

 

DOI: 10.1016/j.jorganchem.2018.01.059


 

 

Yang, B., Senchenkova, S.N., Naumenko, O.I., Shashkov, A.S., Liu, B., Perepelov, A.V., Knirel, Y.A.

Structural and genetic relatedness of the O-antigens of Escherichia coli O50 and O2

(2018) Carbohydrate Research, 464, pp. 8-11.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047182679&doi=10.1016%2fj.carres.2018.05.001&partnerID=40&md5=d41b4f9629fae58936207b8b0782f9f6

 

DOI: 10.1016/j.carres.2018.05.001


 

 

Zdorovenko, E.L., Golomidova, A.K., Prokhorov, N.S., Shashkov, A.S., Wang, L., Letarov, A.V., Knirel, Y.A.

Corrigendum to “Structure of the O-polysaccharide of Escherichia coli O87” [Carbohydr. Res. 412 (2015) 15–18](S0008621515001299)(10.1016/j.carres.2015.04.014)

(2018) Carbohydrate Research, 464, p. 1.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047074018&doi=10.1016%2fj.carres.2018.04.013&partnerID=40&md5=b1f42a646705711babf4b627c014b93a

 

DOI: 10.1016/j.carres.2018.04.013


 

 

Motornov, V.A., Tabolin, A.A., Novikov, R.A., Shepel, N.E., Nenajdenko, V.G., Ioffe, S.L.

Synthesis of 2,5-diaryl-4-halo-1,2,3-triazoles and comparative study of their fluorescent properties

(2018) Tetrahedron, 74 (28), pp. 3897-3903.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047794484&doi=10.1016%2fj.tet.2018.05.071&partnerID=40&md5=5a1470601616e88f42b49f3de8705f91

 

DOI: 10.1016/j.tet.2018.05.071


 

 

Supranovich, V.I., Levin, V.V., Struchkova, M.I., Hu, J., Dilman, A.D.

Visible light-mediated difluoroalkylation of electron-deficient alkenes

(2018) Beilstein Journal of Organic Chemistry, 14, pp. 1637-1641. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049722838&doi=10.3762%2fbjoc.14.139&partnerID=40&md5=c732f8b5d8d11719ab894547b09e6f98

 

DOI: 10.3762/bjoc.14.139


 

 

Gurskii, M.E., Kolomnikova, G.D., Baranin, S.V., Bubnov, Y.N.

Synthesis of 3,5-dimethyl-1-boraadamantane and its transformation into 3,5-dimethyl-1-azaadamantane

(2018) Mendeleev Communications, 28 (4), pp. 366-368.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051050620&doi=10.1016%2fj.mencom.2018.07.008&partnerID=40&md5=443ef214048a15cebf0bd941b0ab540a

 

DOI: 10.1016/j.mencom.2018.07.008


 

 

Kustov, L.M., Kustov, A.L., Kazansky, V.B., Kustov, L.M.

Spectroscopic investigation of redox and acidic properties of Co-substituted aluminophosphate CoAPO-11

(2018) Mendeleev Communications, 28 (4), pp. 354-356.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051191750&doi=10.1016%2fj.mencom.2018.07.003&partnerID=40&md5=01325c5ab411f8c89b331c27cf968131

 

DOI: 10.1016/j.mencom.2018.07.003


 

 

Shkineva, T.K., Kormanov, A.V., Boldinova, V.N., Vatsadze, I.A., Dalinger, I.L.

Synthesis of 4,4'-dinitro-1H,1'H-[3,3'-bipyrazole]-5,5'-diamine

(2018) Chemistry of Heterocyclic Compounds, 54 (7), pp. 703-709.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053241617&doi=10.1007%2fs10593-018-2336-5&partnerID=40&md5=1d77e7dd64559a6d9ed4fcb9b62bde16

 

DOI: 10.1007/s10593-018-2336-5


 

 

Vereshchagin, A.N., Karpenko, K.A., Elinson, M.N., Dorofeeva, E.O., Goloveshkin, A.S., Egorov, M.P.

Pseudo six-component stereoselective synthesis of 2,4,6-triaryl-3,3,5,5-tetracyanopiperidines

(2018) Mendeleev Communications, 28 (4), pp. 384-386. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051052552&doi=10.1016%2fj.mencom.2018.07.014&partnerID=40&md5=07d8881077e18810fcf179fe9e2f1c5b

 

DOI: 10.1016/j.mencom.2018.07.014


 

 

Elinson, M.N., Vereshchagin, A.N., Anisina, Y.E., Goloveshkin, A.S., Ushakov, I.E., Egorov, M.P.

PASE facile and efficient multicomponent approach to the new type of 5-C-substituted 2,4-diamino-5H-chromeno[2,3-b]pyridine scaffold

(2018) Mendeleev Communications, 28 (4), pp. 372-374.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051013480&doi=10.1016%2fj.mencom.2018.07.010&partnerID=40&md5=874730153519d9b9a141b4062e40a36a

 

DOI: 10.1016/j.mencom.2018.07.010


 

 

Gorbunov, Y.О., Lichitsky, B.V., Komogortsev, A.N., Mityanov, V.S., Dudinov, A.А., Krayushkin, M.M.

Synthesis of Condensed Furylacetic Acids Based on Multicomponent Condensation of Heterocyclic Enols with Arylglyoxals and Meldrum's Acid

(2018) Chemistry of Heterocyclic Compounds, 54 (7), pp. 692-695.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053280210&doi=10.1007%2fs10593-018-2333-8&partnerID=40&md5=3d752479ceff4d3aec4535ea5c992264

 

DOI: 10.1007/s10593-018-2333-8


 

 

Eliseev, O.L., Savost'yanov, A.P., Sulima, S.I., Lapidus, A.L.

Recent development in heavy paraffin synthesis from CO and H2

(2018) Mendeleev Communications, 28 (4), pp. 345-351.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051001685&doi=10.1016%2fj.mencom.2018.07.001&partnerID=40&md5=a078140ac6520b1a5207b941fed158d1

 

DOI: 10.1016/j.mencom.2018.07.001


 

 

Dutov, M.D., Kachala, V.V., Ugrak, B.I., Korolev, V.A., Popkov, S.V., Aleksanyan, D.R., Rusina, O.N., Aleksanyan, K.G., Koshelev, V.N.

Synthesis and fungicidal activity of new 4-hydroxy-6-trifluoromethyl-2-phenylindoles

(2018) Mendeleev Communications, 28 (4), pp. 437-438.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051044843&doi=10.1016%2fj.mencom.2018.07.033&partnerID=40&md5=380c5b16c3956b5f244eb62a9a7162e7

 

DOI: 10.1016/j.mencom.2018.07.033


 

 

Iakovenko, R.O., Dilman, A.D.

Synthesis of halodifluoromethyl-substituted phosphines

(2018) Mendeleev Communications, 28 (4), pp. 396-397.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051002148&doi=10.1016%2fj.mencom.2018.07.018&partnerID=40&md5=bd179edc15a5b5ad35a52ff0891859cc

 

DOI: 10.1016/j.mencom.2018.07.018


 

 

Aliev, S.B., Gurskiy, S.I., Zakharov, V.N., Кustov, L.М.

Synthesis of novel nanoporous metal-organic gels with tunable porosity and sensing of aromatic compounds

(2018) Microporous and Mesoporous Materials, 264, pp. 112-117.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041487925&doi=10.1016%2fj.micromeso.2018.01.001&partnerID=40&md5=01f0ce1cabfe8ba85e036684d6552c11

 

DOI: 10.1016/j.micromeso.2018.01.001


 

 

Kitai, M.S., Volkov, W.W., Zharov, A.A., Zubavichus, Y.V., Konarev, P.V., Nazarov, M.M., Polunin, E.V., Pogodina, Y.E., Sokolov, V.I.

Optical Properties of Amorphous Perfluorinated Polymers in the Terahertz Range

(2018) Journal of Applied Spectroscopy, 85 (3), pp. 374-380.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051054715&doi=10.1007%2fs10812-018-0660-2&partnerID=40&md5=1cc542820aa8994515100cf8daaf8fa9

 

DOI: 10.1007/s10812-018-0660-2


 

 

Zaremski, M.Y., Odintsova, V.V., Bol’shakova, A.V., Garina, E.S., Gurskii, M.E., Bubnov, Y.N.

Polymerization of Methyl Methacrylate in the Presence of Boroxyl Radicals. Synthesis of Block Copolymers

(2018) Polymer Science - Series B, 60 (4), pp. 436-444.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052148910&doi=10.1134%2fS1560090418040127&partnerID=40&md5=2ca6caa29bffd4aa0c56fec51c4e06fb

 

DOI: 10.1134/S1560090418040127


 

 

Gibadullina, N.N., Latypova, D.R., Vakhitov, V.A., Khasanova, D.V., Zainullina, L.F., Vakhitova, Y.V., Lobov, A.N., Ugrak, B.I., Tomilov, Y.V., Dokichev, V.A.

Synthesis and cytotoxic activities of difluoroacetyl-substituted hexahydropyrimidine derivatives

(2018) Journal of Fluorine Chemistry, 211, pp. 94-99.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046150406&doi=10.1016%2fj.jfluchem.2018.04.011&partnerID=40&md5=c65ea709389ec42d14c25974d37ca26c

 

DOI: 10.1016/j.jfluchem.2018.04.011


 

 

Naumovich, Y.A., Kokuev, A.O., Sukhorukov, A.Y., Ioffe, S.L.

Synthesis of α-Thiooximes by Addition of Thiols to N, N -Bis(oxy)-enamines: A Comparative Study of S-, N-, and O-Nucleoa-philes in Michael Reaction with Nitrosoalkene Species

(2018) Synlett, 29 (10), pp. 1334-1339.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045329966&doi=10.1055%2fs-0036-1591973&partnerID=40&md5=f2c4c004f79e7ecd28de8f9349630eeb

 

DOI: 10.1055/s-0036-1591973


 

 

Stogniy, M.Y., Suponitsky, K.Y., Chizhov, A.O., Sivaev, I.B., Bregadze, V.I.

Synthesis of 8-alkoxy and 8,8′-dialkoxy derivatives of cobalt bis(dicarbollide)

(2018) Journal of Organometallic Chemistry, 865, pp. 138-144. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042942141&doi=10.1016%2fj.jorganchem.2018.03.005&partnerID=40&md5=754ea9977195ac18d18fac7a134c2e81

 

DOI: 10.1016/j.jorganchem.2018.03.005


 

 

Jana, S., Chakraborty, A., Shirinian, V.Z., Hajra, A.

Synthesis of Benzo[4,5]imidazo[2,1-b]thiazole by Copper(II)-Catalyzed Thioamination of Nitroalkene with 1H-Benzo[d]imidazole-2-thiol

(2018) Advanced Synthesis and Catalysis, 360 (12), pp. 2402-2408.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046350524&doi=10.1002%2fadsc.201800393&partnerID=40&md5=0554271cb5b84977320418acd4a052ac

 

DOI: 10.1002/adsc.201800393


 

 

Naumenko, O.I., Guo, X., Senchenkova, S.N., Geng, P., Perepelov, A.V., Shashkov, A.S., Liu, B., Knirel, Y.A.

Structure and gene cluster of the O-antigen of Escherichia coli O54

(2018) Carbohydrate Research, 462, pp. 34-38.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045407176&doi=10.1016%2fj.carres.2018.04.001&partnerID=40&md5=2fbf8fb0eceb2659fd2cf4a860cc210c

 

DOI: 10.1016/j.carres.2018.04.001


 

 

Makhova, N.N., Fershtat, L.L.

Recent advances in the synthesis and functionalization of 1,2,5-oxadiazole 2-oxides

(2018) Tetrahedron Letters, 59 (24), pp. 2317-2326. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046812768&doi=10.1016%2fj.tetlet.2018.04.070&partnerID=40&md5=1ae6f68278ee529c9d1360ef76ebc3d7

 

DOI: 10.1016/j.tetlet.2018.04.070


 

 

Smolenskii, E.A., Ryzhov, A.N., Chuvaeva, I.V., Maslova, L.K., Lapidus, A.L.

The necessary and sufficient conditions for chemical equilibrium

(2018) Russian Chemical Bulletin, 67 (6), pp. 966-971.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053899789&doi=10.1007%2fs11172-018-2165-9&partnerID=40&md5=497b3a092da23ac503b017f30a8254f6

 

DOI: 10.1007/s11172-018-2165-9


 

 

Gordeev, E.G., Galushko, A.S., Ananikov, V.P.

Improvement of quality of 3D printed objects by elimination of microscopic structural defects in fused deposition modeling

(2018) PLoS ONE, 13 (6), статья № e0198370, . Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048174217&doi=10.1371%2fjournal.pone.0198370&partnerID=40&md5=d4cbf965c78baed3e1fa2e7a228c6f68

 

DOI: 10.1371/journal.pone.0198370


 

 

Kulikov, A.S., Epishina, M.A., Fershtat, L.L., Makhova, N.N.

Effective synthesis of 7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazines

(2018) Chemistry of Heterocyclic Compounds, 54 (6), pp. 669-672.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051293766&doi=10.1007%2fs10593-018-2325-8&partnerID=40&md5=a7a900713f4cd9809559367863b83254

 

DOI: 10.1007/s10593-018-2325-8


 

 

Komkov, A.V., Chizhov, A.O., Shashkov, A.S., Zavarzin, I.V.

Synthesis of androsteno[17,16-d]pyrazoles and androsteno[17,16-d]-2′-pyrazolines with pyrazolo[3,4-d]pyrimidine fragments

(2018) Russian Chemical Bulletin, 67 (6), pp. 1088-1099.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053934856&doi=10.1007%2fs11172-018-2185-5&partnerID=40&md5=7efe4969202dc14a11e91457be38a8de

 

DOI: 10.1007/s11172-018-2185-5


 

 

Parakhin, V.V., Gordeev, P.B., Luk’yanov, O.A.

3-(1-Methyl-1-nitroethyl-1-ONN-azoxy)-4-aminofuroxan. Synthesis and transformations of the amino group

(2018) Russian Chemical Bulletin, 67 (6), pp. 1065-1071.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053932750&doi=10.1007%2fs11172-018-2181-9&partnerID=40&md5=29d42dd2a21aefa3fd62beb2dc042846

 

DOI: 10.1007/s11172-018-2181-9


 

 

Anikin, N.A., Andreev, A.M., Kuz’minskii, M.B., Mendkovich, A.S.

A new approach for the acceleration of large-scale serial quantum chemical calculations of docking complexes

(2018) Russian Chemical Bulletin, 67 (6), pp. 1100-1103.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053856191&doi=10.1007%2fs11172-018-2186-4&partnerID=40&md5=57cd46e301221ead3ee64ebaf1384f88

 

DOI: 10.1007/s11172-018-2186-4


 

 

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Shashkov, A.S., Nifantiev, N.E., Usov, A.I.

Two structurally similar fucosylated chondroitin sulfates from the holothurian species Stichopus chloronotus and Stichopus horrens

(2018) Carbohydrate Polymers, 189, pp. 10-14. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041520194&doi=10.1016%2fj.carbpol.2018.02.008&partnerID=40&md5=04ed09eccc83098796ac233c96c67d8b

 

DOI: 10.1016/j.carbpol.2018.02.008


 

 

Chirkova, Z.V., Kabanova, M.V., Filimonov, S.I., Samet, A.V., Stashina, G.A., Sudzilovskaya, T.N.

Chlorination of 2-substituted 1-hydroxyindoles

(2018) Russian Chemical Bulletin, 67 (6), pp. 1083-1087.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053838235&doi=10.1007%2fs11172-018-2184-6&partnerID=40&md5=1e00de8fb0393d511a497e2d8bb3972a

 

DOI: 10.1007/s11172-018-2184-6


 

 

Elinson, M.N., Vereshchagin, A.N., Korshunov, A.D., Zaimovskaya, T.A., Egorov, M.P.

Electrochemical cascade assembling of heterocyclic ketones and two molecules of malononitrile: facile and efficient ‘one-pot’ approach to 6-heterospiro[2.5]octane-1,1,2,2-tetracarbonitrile scaffold

(2018) Monatshefte fur Chemie, 149 (6), pp. 1069-1074.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042074171&doi=10.1007%2fs00706-018-2158-2&partnerID=40&md5=2ac399122a3e4987cf53833d1c2947e1

 

DOI: 10.1007/s00706-018-2158-2


 

 

Guranova, N.I., Borisova, T.N., Novikov, R.A., Sorokina, E.A., Khrustalev, V.N., Varlamov, A.V.

Reactions of thieno[2,3-с]pyrrolines with dehydrobenzene

(2018) Chemistry of Heterocyclic Compounds, 54 (6), pp. 664-668.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051291426&doi=10.1007%2fs10593-018-2324-9&partnerID=40&md5=9e7bd66f0d8e1efe3af3e394b5c00d6a

 

DOI: 10.1007/s10593-018-2324-9


 

 

Belyy, A.Y., Platonov, D.N., Salikov, R.F., Levina, A.A., Tomilov, Y.V.

A New Simple Procedure for the Synthesis of Heptamethyl Cyclohepta-1,3,5-triene-1,2,3,4,5,6,7-heptacarboxylate

(2018) Synlett, 29 (9), pp. 1157-1160. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044345082&doi=10.1055%2fs-0036-1591962&partnerID=40&md5=e185999762700a0384ff43542cfea2df

 

DOI: 10.1055/s-0036-1591962


 

 

Altova, E.P., Kuznetsov, V.V., Marochkin, I.I., Rykov, A.N., Makhova, N.N., Shishkov, I.F.

3-Cyclopropyl-1,2-dimethyldiaziridine: synthesis and study of molecular structure by gas electron diffraction method

(2018) Structural Chemistry, 29 (3), pp. 815-822. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044243437&doi=10.1007%2fs11224-018-1104-6&partnerID=40&md5=21b5f7eddaf3de0750e4765903aad9cf

 

DOI: 10.1007/s11224-018-1104-6


 

 

Mishanin, I.I., Zizganova, A.I., Bogdan, V.I.

Oxidative dehydrogenation of ethane to ethylene with carbon dioxide over supported Ga, Fe, and Cr-containing catalysts

(2018) Russian Chemical Bulletin, 67 (6), pp. 1031-1034.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053862195&doi=10.1007%2fs11172-018-2175-7&partnerID=40&md5=c5ccc1fe3cc1401b28cdfde84fe83164

 

DOI: 10.1007/s11172-018-2175-7


 

 

Gazieva, G.A., Nechaeva, T.V., Kostikova, N.N., Sigay, N.V., Serkov, S.A., Popkov, S.V.

Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils

(2018) Russian Chemical Bulletin, 67 (6), pp. 1059-1064.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053883148&doi=10.1007%2fs11172-018-2180-x&partnerID=40&md5=8df6c1f2dc573f59fd014cf8cee3b870

 

DOI: 10.1007/s11172-018-2180-x


 

 

Kovalenko, A.A., Nelyubina, Y.V., Korlyukov, A.A., Lyssenko, K.A., Ananyev, I.V.

The truth is out there: The metal-π interactions in crystal of Cr(CO)3(pcp) as revealed by the study of vibrational smearing of electron density

(2018) Zeitschrift fur Kristallographie - Crystalline Materials, 233 (5), pp. 317-336.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85037848173&doi=10.1515%2fzkri-2017-2085&partnerID=40&md5=3c96e23f4d28875d2a43621ff5ab6f25

 

DOI: 10.1515/zkri-2017-2085


 

 

Naumenko, O.I., Zheng, H., Xiong, Y., Senchenkova, S.N., Wang, H., Shashkov, A.S., Li, Q., Wang, J., Knirel, Y.A.

Studies on the O-polysaccharide of Escherichia albertii O2 characterized by non-stoichiometric O-acetylation and non-stoichiometric side-chain L-fucosylation

(2018) Carbohydrate Research, 461, pp. 80-84.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044597296&doi=10.1016%2fj.carres.2018.02.013&partnerID=40&md5=6f70b0a181757cca74def482e352c509

 

DOI: 10.1016/j.carres.2018.02.013


 

 

Chilingarov, N.S., Zhirov, M.S., Shmykova, A.M., Martynova, E.A., Glukhov, L.M., Chernikova, E.A., Kustov, L.M., Markov, V.Y., Ioutsi, V.A., Sidorov, L.N.

Evaporation Study of an Ionic Liquid with a Double-Charged Cation

(2018) Journal of Physical Chemistry A, 122 (19), pp. 4622-4627.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047546639&doi=10.1021%2facs.jpca.8b02488&partnerID=40&md5=0e032d4b57ba883b6882ce978efe2ae6

 

DOI: 10.1021/acs.jpca.8b02488


 

 

Barsegyan, Y.A., Baranov, V.V., Kravchenko, A.N., Strelenko, Y.A., Anikina, L.V., Karnoukhova, V.A., Kolotyrkina, N.G.

Synthesis, Structure, and Biological Activity of 2,6-Disubstituted 2,3a,4a,6,7a,8a-Hexaazaperhydrocyclopenta[ def ]fluorene-4-thioxo-8-ones

(2018) Synthesis (Germany), 50 (10), pp. 2099-2105.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046160126&doi=10.1055%2fs-0036-1591952&partnerID=40&md5=f089ca0ca3fcd4171fe4ab114a12444a

 

DOI: 10.1055/s-0036-1591952


 

 

Dilman, A.D., Levin, V.V.

Difluorocarbene as a Building Block for Consecutive Bond-Forming Reactions

(2018) Accounts of Chemical Research, 51 (5), pp. 1272-1280. Цитировано 12 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047221357&doi=10.1021%2facs.accounts.8b00079&partnerID=40&md5=34699df284ed88ba59d4a6b01b2db1b3

 

DOI: 10.1021/acs.accounts.8b00079


 

 

Akchurin, I.O., Yakhutina, A.I., Bochkov, A.Y., Solovjova, N.P., Medvedev, M.G., Traven, V.F.

Novel push-pull fluorescent dyes – 7-(diethylamino)furo- and thieno[3,2-c]coumarins derivatives: structure, electronic spectra and TD-DFT study

(2018) Journal of Molecular Structure, 1160, pp. 215-221.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041498340&doi=10.1016%2fj.molstruc.2018.01.086&partnerID=40&md5=d81c3ec4801aa80af9fa7b14aa6bd062

 

DOI: 10.1016/j.molstruc.2018.01.086


 

 

Kravchenko, A.N., Vasilevskii, S.V., Gazieva, G.A., Baranov, V.V., Barachevsky, V.A., Kobeleva, O.I., Venidiktova, O.V., Karnoukhova, V.A.

Transformations of S-substituted 5,7-dimethyl-4а,5а-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-2-ones under treatment of 1,2-benzoquinones and photochemical properties of reaction products

(2018) Tetrahedron, 74 (19), pp. 2359-2368.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044844743&doi=10.1016%2fj.tet.2018.03.056&partnerID=40&md5=bb619f1fc4db3abd61a6e5af7258d2c8

 

DOI: 10.1016/j.tet.2018.03.056


 

 

Seitkalieva, M.M., Kashin, A.S., Egorova, K.S., Ananikov, V.P.

Micro-scale processes occurring in ionic liquid–water phases during extraction

(2018) Separation and Purification Technology, 196, pp. 318-326. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021418027&doi=10.1016%2fj.seppur.2017.06.056&partnerID=40&md5=0ef62cfe02e6d0a74e578ac011222dcb

 

DOI: 10.1016/j.seppur.2017.06.056


 

 

Coghi, P., Yaremenko, I.A., Prommana, P., Radulov, P.S., Syroeshkin, M.A., Wu, Y.J., Gao, J.Y., Gordillo, F.M., Mok, S., Wong, V.K.W., Uthaipibull, C., Terent'ev, A.O.

Novel Peroxides as Promising Anticancer Agents with Unexpected Depressed Antimalarial Activity

(2018) ChemMedChem, 13 (9), pp. 902-908.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046543665&doi=10.1002%2fcmdc.201700804&partnerID=40&md5=92cbf7997856615b266dc578b85bfe92

 

DOI: 10.1002/cmdc.201700804


 

 

Dalinger, I.L., Kormanov, A.V., Suponitsky, K.Y., Muravyev, N.V., Sheremetev, A.B.

Pyrazole–Tetrazole Hybrid with Trinitromethyl, Fluorodinitromethyl, or (Difluoroamino)dinitromethyl Groups: High-Performance Energetic Materials

(2018) Chemistry - An Asian Journal, 13 (9), pp. 1165-1172. Цитировано 7 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044854620&doi=10.1002%2fasia.201800214&partnerID=40&md5=935ecbb816c5ce116931796e7a06a570

 

DOI: 10.1002/asia.201800214


 

 

Sizova, O.V., Shashkov, A.S., Kondakova, A.N., Knirel, Y.A., Shaikhutdinova, R.Z., Ivanov, S.A., Kislichkina, A.A., Kadnikova, L.A., Bogun, A.G., Dentovskaya, S.V.

Full structure and insight into the gene cluster of the O-specific polysaccharide of Yersinia intermedia H9-36/83 (O:17)

(2018) Carbohydrate Research, 460, pp. 51-56.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042919179&doi=10.1016%2fj.carres.2018.02.014&partnerID=40&md5=991bb510e1295d1b714cb7ae42d1b8da

 

DOI: 10.1016/j.carres.2018.02.014


 

 

Senchenkova, S.N., Hou, W., Naumenko, O.I., Geng, P., Shashkov, A.S., Perepelov, A.V., Yang, B., Knirel, Y.A.

Structure and genetics of a glycerol 2-phosphate-containing O-specific polysaccharide of Escherichia coli O33

(2018) Carbohydrate Research, 460, pp. 47-50.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042923885&doi=10.1016%2fj.carres.2018.02.008&partnerID=40&md5=d23fdcc22b03bde7ee3398aa6a9122fc

 

DOI: 10.1016/j.carres.2018.02.008


 

 

Kalugin, V.E., Shestopalov, A.M.

The synthesis of substituted 5-aminopyrido[3′,2′:4,5]thieno[3,2-c]isoquinolines and their sulfinyl and sulfonyl derivatives

(2018) Russian Chemical Bulletin, 67 (5), pp. 902-911.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051755072&doi=10.1007%2fs11172-018-2155-y&partnerID=40&md5=cc9b113a34b19b4ebb439a95088fc22d

 

DOI: 10.1007/s11172-018-2155-y


 

 

Vasil’ev, A.A., Kuchurov, I.V., Zlotin, S.G.

1,4-cis-Hydrogenation of butyl sorbate in supercritical carbon dioxide

(2018) Russian Chemical Bulletin, 67 (5), pp. 923-926.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051870206&doi=10.1007%2fs11172-018-2158-8&partnerID=40&md5=64e00259f025e70e728be1e2459e1b4b

 

DOI: 10.1007/s11172-018-2158-8


 

 

Shchetinina, M.A., Chernoburova, E.I., Kolotyrkina, N.G., Dzhafarov, M.K., Vasilevich, F.I., Zavarzin, I.V.

Synthesis of sodium 5-sulfate-ivermectin and disodium 4″,5-disulfate-ivermectin

(2018) Russian Chemical Bulletin, 67 (5), pp. 836-839.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051840202&doi=10.1007%2fs11172-018-2146-z&partnerID=40&md5=384b95a942198155f6194a7dfeaabce3

 

DOI: 10.1007/s11172-018-2146-z


 

 

Dutov, M.D., Aleksanyan, D.R., Serushkina, O.V., Nesterova, E.N., Shevelev, S.A.

Reactions of 1,3,5-trinitrobenzene with primary aliphatic alcohols

(2018) Russian Chemical Bulletin, 67 (5), pp. 822-825.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051872906&doi=10.1007%2fs11172-018-2143-2&partnerID=40&md5=bc227ad323fc1515a522b81eb86d9ae0

 

DOI: 10.1007/s11172-018-2143-2


 

 

Blinnikov, A.N., Chernoburova, E.I., Kolotyrkina, N.G., Shchetinina, M.A., Lishchuk, V.A., Ovchinnikov, K.L., Kolobov, A.V., Dzhafarov, M.K., Vasilevich, F.I., Zavarzin, I.V.

Synthesis of ivermectin-4″,5-diyl[bis(N-methylcarbamate)]

(2018) Russian Chemical Bulletin, 67 (5), pp. 833-835.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051864051&doi=10.1007%2fs11172-018-2145-0&partnerID=40&md5=e5b35aa47c97fb52330019c1b1e72f53

 

DOI: 10.1007/s11172-018-2145-0


 

 

Elinson, M.N., Ryzhkov, F.V., Vereshchagin, A.N., Goloveshkin, A.S., Bushmarinov, I.S., Egorov, M.P.

Efficient and facile ‘on-solvent’ multicomponent synthesis of medicinally privileged pyrano[3,2-c]pyridine scaffold

(2018) Research on Chemical Intermediates, 44 (5), pp. 3199-3209.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041128049&doi=10.1007%2fs11164-018-3301-8&partnerID=40&md5=cc17527ebf9afd3058e7308bc9ccd764

 

DOI: 10.1007/s11164-018-3301-8


 

 

Anikina, L.V., Vikharev, Y.B., Baranov, V.V., Malyshev, O.R., Kravchenko, A.N.

Preparative synthesis and pharmacological activity of Albicar racemate and enantiomers

(2018) Mendeleev Communications, 28 (3), pp. 317-319. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047611987&doi=10.1016%2fj.mencom.2018.05.030&partnerID=40&md5=782815a0222f3e4edc264bad62778297

 

DOI: 10.1016/j.mencom.2018.05.030


 

 

Andrianova, A.A., Maslova, Y.D., Novikov, M.A., Semenov, S.E., Nefedov, O.M.

(NHC)AgCl catalyzed bromofluorocyclopropanation of alkenes with CFBr2CO2Na

(2018) Journal of Fluorine Chemistry, 209, pp. 49-55.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042704280&doi=10.1016%2fj.jfluchem.2018.02.001&partnerID=40&md5=74eadec68fc27ad8a04bd3ca457df87d

 

DOI: 10.1016/j.jfluchem.2018.02.001


 

 

Eliseev, O.L., Bondarenko, T.N., Britvin, S.N., Khodorchenko, P.P., Lapidus, A.L.

Efficient water-soluble catalytic system RhI-CAP for biphasic hydroformylation of olefins

(2018) Mendeleev Communications, 28 (3), pp. 264-266.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047640366&doi=10.1016%2fj.mencom.2018.05.011&partnerID=40&md5=f7ee664d832aa3ef9d22d153f7ddddb0

 

DOI: 10.1016/j.mencom.2018.05.011


 

 

Tarasov, A.L., Tkachenko, O.P., Kustov, L.M.

Mono and Bimetallic Pt–(M)/Al2O3 Catalysts for Dehydrogenation of Perhydro-N-ethylcarbazole as the Second Stage of Hydrogen Storage

(2018) Catalysis Letters, 148 (5), pp. 1472-1477.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042924138&doi=10.1007%2fs10562-018-2325-4&partnerID=40&md5=10dfb055f1693a1139ea936e5f8713ca

 

DOI: 10.1007/s10562-018-2325-4


 

 

Samet, A.V., Sil’yanova, E.A., Ushkarov, V.I., Semenova, M.N., Semenov, V.V.

Synthesis of 3,4-diaryl- and 4-acyl-3-arylpyrroles and study of their antimitotic activity

(2018) Russian Chemical Bulletin, 67 (5), pp. 858-865.

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DOI: 10.1007/s11172-018-2150-3


 

 

Kustov, L.M., Finashina, E.D., Avaev, V.I., Ershov, B.G.

Decalin ring opening on Pt-Ru/SiO2 catalysts

(2018) Fuel Processing Technology, 173, pp. 270-275.

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DOI: 10.1016/j.fuproc.2018.02.007


 

 

Marjewski, A.A., Medvedev, M.G., Gerasimov, I.S., Panova, M.V., Perdew, J.P., Lyssenko, K.A., Dmitrienko, A.O.

Interplay between test sets and statistical procedures in ranking DFT methods: The case of electron density studies

(2018) Mendeleev Communications, 28 (3), pp. 225-235.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047604705&doi=10.1016%2fj.mencom.2018.05.001&partnerID=40&md5=fd27e940462c7d64e6592554758b7af2

 

DOI: 10.1016/j.mencom.2018.05.001


 

 

Elinson, M.N., Vereshchagin, A.N., Korshunov, A.D., Egorov, M.P.

A fast and efficient 'on-solvent' cascade assembling of salicylaldehydes and dimethylbarbituric acid into 5-(1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno[2,3-d]pyrimidin-5-yl)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-triones

(2018) Heterocyclic Communications, 24 (2), pp. 79-83.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85043278823&doi=10.1515%2fhc-2018-0015&partnerID=40&md5=e9d5b320de9c66e9eaed1bc81fd98b05

 

DOI: 10.1515/hc-2018-0015


 

 

Yaremenko, I.A., Gomes, G.D.P., Radulov, P.S., Belyakova, Y.Y., Vilikotskiy, A.E., Vil, V.A., Korlyukov, A.A., Nikishin, G.I., Alabugin, I.V., Terent'Ev, A.O.

Ozone-Free Synthesis of Ozonides: Assembling Bicyclic Structures from 1,5-Diketones and Hydrogen Peroxide

(2018) Journal of Organic Chemistry, 83 (8), pp. 4402-4426. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045735106&doi=10.1021%2facs.joc.8b00130&partnerID=40&md5=846139929d388a2d67c48e68c8174d27

 

DOI: 10.1021/acs.joc.8b00130


 

 

Voronin, V.V., Ledovskaya, M.S., Gordeev, E.G., Rodygin, K.S., Ananikov, V.P.

[3+2]-cycloaddition of in situ generated nitrile imines and acetylene for assembling of 1,3-disubstituted pyrazoles with quantitative deuterium labeling

(2018) Journal of Organic Chemistry, 83 (7), pp. 3819-3828. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045097358&doi=10.1021%2facs.joc.8b00155&partnerID=40&md5=34e924e13620c77000385ca3e5741294

 

DOI: 10.1021/acs.joc.8b00155


 

 

Abramenko, N.B., Demidova, T.B., Abkhalimov, Е.V., Ershov, B.G., Krysanov, E.Y., Kustov, L.M.

Ecotoxicity of different-shaped silver nanoparticles: Case of zebrafish embryos

(2018) Journal of Hazardous Materials, 347, pp. 89-94. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85039723620&doi=10.1016%2fj.jhazmat.2017.12.060&partnerID=40&md5=f6c47382faef678e35fcee4bb5574ecb

 

DOI: 10.1016/j.jhazmat.2017.12.060


 

 

Serushkin, V.V., Sinditskii, V.P., Hoang, T.H., Filatov, S.A., Shipulina, A.S., Dalinger, I.L., Shakhnes, A.K., Sheremetev, A.B.

Thermal and combustion behavior of novel oxygen-rich energetic pyrazoles

(2018) Journal of Thermal Analysis and Calorimetry, 132 (1), pp. 127-142. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85039551353&doi=10.1007%2fs10973-017-6911-2&partnerID=40&md5=09046ffca8cc378b57ee7af0d148e6eb

 

DOI: 10.1007/s10973-017-6911-2


 

 

Tuleuov, B.I., Zavarzin, I.V., Shashkov, A.S., Chernoburova, E.I., Adekenov, S.M.

3α,14α,22R,25-Tetrahydroxy-5β(H)-cholest-7-en-6-one, a phytoecdysteroid from Acanthophyllum gypsophiloides possessing anti-inflammatory and analgesic activities

(2018) Russian Chemical Bulletin, 67 (4), pp. 663-666.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049997542&doi=10.1007%2fs11172-018-2120-9&partnerID=40&md5=bfe74280f35d83f62d411489a6acce14

 

DOI: 10.1007/s11172-018-2120-9


 

 

Kustov, L., Golubeva, V., Korableva, A., Anischenko, O., Yegorushina, N., Kapustin, G.

Alkaline-modified ZSM-5 zeolite to control hydrocarbon cold-start emission

(2018) Microporous and Mesoporous Materials, 260, pp. 54-58.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85032378798&doi=10.1016%2fj.micromeso.2017.06.050&partnerID=40&md5=9979f1a1a315a1fbd5ac6583978952df

 

DOI: 10.1016/j.micromeso.2017.06.050


 

 

Sidorov, R.A., Shashkov, A.S., Solovyev, P.A., Gorshkova, E.N., Tsydendambaev, V.D.

Evidence of Strict Stereospecificity in the Structure of sn-1,2-Diacyl-3-Acetyl-Glycerols from Euonymus maximowiczianus Seeds Using Nuclear Magnetic Resonance Spectroscopy

(2018) Lipids, 53 (4), pp. 437-445. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046258952&doi=10.1002%2flipd.12025&partnerID=40&md5=805a5748d6a6067b7f8b419c488a5f7f

 

DOI: 10.1002/lipd.12025


 

 

Zabłotni, A., Matusiak, D., Arbatsky, N.P., Moryl, M., Maciejewska, A., Kondakova, A.N., Shashkov, A.S., Ługowski, C., Knirel, Y.A., Różalski, A.

Changes in the lipopolysaccharide of Proteus mirabilis 9B-m (O11a) clinical strain in response to planktonic or biofilm type of growth

(2018) Medical Microbiology and Immunology, 207 (2), pp. 129-139.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041829025&doi=10.1007%2fs00430-018-0534-5&partnerID=40&md5=17a65eb092a1fb742b9b546e50013c6c

 

DOI: 10.1007/s00430-018-0534-5


 

 

Bruk, L., Titov, D., Ustyugov, A., Zubavichus, Y., Chernikova, V., Tkachenko, O., Kustov, L., Murzin, V., Oshanina, I., Temkin, O.

The mechanism of low-temperature oxidation of carbon monoxide by oxygen over the PdCl2-CuCl2/γ-Al2O3 nanocatalyst

(2018) Nanomaterials, 8 (4), статья № 217, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044987240&doi=10.3390%2fnano8040217&partnerID=40&md5=b9de160d9398cceeb6f0d4c5fe39be08

 

DOI: 10.3390/nano8040217


 

 

Kalenchuk, A.N., Bogdan, V.I., Dunaev, S.F., Kustov, L.M.

Effect of surface hydrophilization on Pt/Sibunit catalytic activity in bicyclohexyl dehydrogenation in hydrogen storage application

(2018) International Journal of Hydrogen Energy, 43 (12), pp. 6191-6196. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042565141&doi=10.1016%2fj.ijhydene.2018.01.121&partnerID=40&md5=fc01d61c611c782303bbdedbb133faf8

 

DOI: 10.1016/j.ijhydene.2018.01.121


 

 

Komarova, B.S., Dorokhova, V.S., Tsvetkov, Y.E., Nifantiev, N.E.

Synthesis of a biotinylated penta-α-(1→6)-d-glucoside based on the rational design of an α-stereoselective glucosyl donor

(2018) Organic Chemistry Frontiers, 5 (6), pp. 909-928. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85043754636&doi=10.1039%2fc7qo01007a&partnerID=40&md5=76a12311db69c552be2f66a4bdb8d35b

 

DOI: 10.1039/c7qo01007a


 

 

Chernavskii, P.A., Pankina, G.V., Kazantsev, R.V., Eliseev, O.L.

Potassium as a Structural Promoter for an Iron/Activated Carbon Catalyst: Unusual Effect of Component Deposition Order on Magnetite Particle Size and Catalytic Behavior in Fischer–Tropsch Synthesis

(2018) ChemCatChem, 10 (6), pp. 1313-1320. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042004812&doi=10.1002%2fcctc.201701818&partnerID=40&md5=6805b9d4d26d5184fbf1061a1c4838e7

 

DOI: 10.1002/cctc.201701818


 

 

Vil', V.A., dos Passos Gomes, G., Bityukov, O.V., Lyssenko, K.A., Nikishin, G.I., Alabugin, I.V., Terent'ev, A.O.

Interrupted Baeyer–Villiger Rearrangement: Building A Stereoelectronic Trap for the Criegee Intermediate

(2018) Angewandte Chemie - International Edition, 57 (13), pp. 3372-3376. Цитировано 8 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042383204&doi=10.1002%2fanie.201712651&partnerID=40&md5=f6e8326aa2b3738c218707e0da317e3b

 

DOI: 10.1002/anie.201712651


 

 

Kapaev, R.R., Toukach, P.V.

GRASS: Semi-Automated NMR-based structure elucidation of saccharides

(2018) Bioinformatics, 34 (6), pp. 957-963. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044255704&doi=10.1093%2fbioinformatics%2fbtx696&partnerID=40&md5=5be879abd3f32cf52d65d3547d11df79

 

DOI: 10.1093/bioinformatics/btx696


 

 

Smirnov, V.O., Maslov, A.S., Kokorekin, V.A., Korlyukov, A.A., Dilman, A.D.

Photoredox generation of the trifluoromethyl radical from borate complexes: Via single electron reduction

(2018) Chemical Communications, 54 (18), pp. 2236-2239.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042656161&doi=10.1039%2fc8cc00245b&partnerID=40&md5=94470615840d5f22e7ead670b5fc914a

 

DOI: 10.1039/c8cc00245b


 

 

Chelysheva, E., Turkina, A., Polushkina, E., Shmakov, R., Zeifman, A., Aleshin, S., Shokhin, I., Guranda, D., Oksenjuk, O., Mordanov, S., Kazakbaeva, K., Chilov, G.

Placental transfer of tyrosine kinase inhibitors used for chronic myeloid leukemia treatment

(2018) Leukemia and Lymphoma, 59 (3), pp. 733-738. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85023756627&doi=10.1080%2f10428194.2017.1347929&partnerID=40&md5=31d5ed113c9f036914d9e7a80ed7cbe2

 

DOI: 10.1080/10428194.2017.1347929


 

 

Zdorovenko, E.L., Shashkov, A.S., Kadykova, A.A., Kiseleva, E.P., Savich, V.V., Novik, G.I., Knirel, Y.A.

Structural analysis of the O-polysaccharide from the lipopolysaccharide of Pseudomonas putida BIM B-1100

(2018) Carbohydrate Research, 457, pp. 8-13. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85039850033&doi=10.1016%2fj.carres.2017.12.009&partnerID=40&md5=7d0f764bb9acb856ee3e308766bc82c5

 

DOI: 10.1016/j.carres.2017.12.009


 

 

Naumenko, O.I., Zheng, H., Wang, J., Senchenkova, S.N., Wang, H., Shashkov, A.S., Chizhov, A.O., Li, Q., Knirel, Y.A., Xiong, Y.

Structure elucidation of the O-specific polysaccharide by NMR spectroscopy and selective cleavage and genetic characterization of the O-antigen of Escherichia albertii O5

(2018) Carbohydrate Research, 457, pp. 25-31. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85039997904&doi=10.1016%2fj.carres.2017.12.010&partnerID=40&md5=1986e9f26ffedd82a1f2a1f551f35875

 

DOI: 10.1016/j.carres.2017.12.010


 

 

Gvozdev, V.D., Shavrin, K.N., Egorov, M.P., Nefedov, O.M.

New selective cyclizations of alk-4-ynals with primary amines and azoles:one-pot synthesis of 2-azolylpyrrolidines and 3-iminocyclopentenes

(2018) Mendeleev Communications, 28 (2), pp. 123-125.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044113668&doi=10.1016%2fj.mencom.2018.03.002&partnerID=40&md5=6dcf4588761d0ba5ed3699beaa35c1fa

 

DOI: 10.1016/j.mencom.2018.03.002


 

 

Vedenyapina, M.D., Kuznetsov, V.V., Rodikova, D.I., Makhova, N.N., Vedenyapin, A.A.

Anodic corrosion of gold in solutions of diaminoalkanes

(2018) Mendeleev Communications, 28 (2), pp. 181-183.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044740390&doi=10.1016%2fj.mencom.2018.03.024&partnerID=40&md5=99f2c1fd837080464f52ae9def575623

 

DOI: 10.1016/j.mencom.2018.03.024


 

 

Boganov, S.E., Promyslov, V.M., Rynin, S.S., Krylova, I.V., Zaitseva, G.S., Egorov, M.P.

Complexes of dichlorosilylene with allyl chloride and allyl bromide: matrix IR spectroscopy and quantum chemical studies

(2018) Russian Chemical Bulletin, 67 (3), pp. 425-443.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049313603&doi=10.1007%2fs11172-018-2089-4&partnerID=40&md5=1c6ee973a6a9111450b42ce30f2a6aa3

 

DOI: 10.1007/s11172-018-2089-4


 

 

Chmovzh, T., Knyazeva, E., Popov, V., Rakitin, O.

4,7-dichloro[1,2,5]oxadiazolo[3,4-d]pyridazine 1-oxide

(2018) MolBank, 2018 (1), статья № M982, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042544045&doi=10.3390%2fM982&partnerID=40&md5=56587df2825c409337f4fa3bc8bd270a

 

DOI: 10.3390/M982


 

 

Kurkin, V.A., Ryazanova, T.K., Daeva, E.D., Kadentsev, V.I.

Constituents of Arctostaphylos uva-ursi Leaves

(2018) Chemistry of Natural Compounds, 54 (2), pp. 278-280.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045132853&doi=10.1007%2fs10600-018-2323-1&partnerID=40&md5=554ed3d254080960d06eaaf50959c195

 

DOI: 10.1007/s10600-018-2323-1


 

 

Gorbunov, Y.О., Komogortsev, А.N., Mityanov, V.S., Lichitskii, B.V., Dudinov, A.A., Lyssenko, K.A., Krayushkin, М.М.

Synthesis of substituted benzofurans by condensation of arylglyoxals with enols and phenols

(2018) Russian Chemical Bulletin, 67 (3), pp. 504-509. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049318668&doi=10.1007%2fs11172-018-2101-z&partnerID=40&md5=27995cf7868aec82f43323695e0facef

 

DOI: 10.1007/s11172-018-2101-z


 

 

Palysaeva, N.V., Boltacheva, N.S., Slepukhin, P.A., Pervova, M.G., Filyakova, V.I., Sheremetev, A.B., Charushin, V.N.

Step by step and one-pot syntheses of 5-hydroxy-5-(polyfluoroalkyl)isoxazol-4(5H)-one oximes

(2018) Mendeleev Communications, 28 (2), pp. 126-127.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044101391&doi=10.1016%2fj.mencom.2018.03.003&partnerID=40&md5=6893b76e88a1b4016a1aa1c5be61f368

 

DOI: 10.1016/j.mencom.2018.03.003


 

 

Vishtorskaya, A.A., Saverina, E.A., Pechennikov, V.M., Krylova, I.V., Lalov, A.V., Syroeshkin, M.A., Egorov, M.P., Jouikov, V.V.

Assessing Ge-132 as an antioxidant in organic and water-containing media

(2018) Journal of Organometallic Chemistry, 858, pp. 8-13.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040664121&doi=10.1016%2fj.jorganchem.2018.01.004&partnerID=40&md5=e450903d347344dde1cdb8c56a1f1984

 

DOI: 10.1016/j.jorganchem.2018.01.004


 

 

Mashkovsky, I.S., Markov, P.V., Bragina, G.O., Baeva, G.N., Rassolov, A.V., Bukhtiyarov, A.V., Prosvirin, I.P., Bukhtiyarov, V.I., Stakheev, A.Y.

PdZn/α-Al2O3 catalyst for liquid-phase alkyne hydrogenation: effect of the solid-state alloy transformation into intermetallics

(2018) Mendeleev Communications, 28 (2), pp. 152-154. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044780235&doi=10.1016%2fj.mencom.2018.03.014&partnerID=40&md5=7d782d722f46a4934eee0d2465a55bdc

 

DOI: 10.1016/j.mencom.2018.03.014


 

 

Evdokimenko, N.D., Kustov, A.L., Kim, K.O., Igonina, M.S., Kustov, L.M.

Direct hydrogenation of CO2 on deposited iron-containing catalysts under supercritical conditions

(2018) Mendeleev Communications, 28 (2), pp. 147-149.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044142478&doi=10.1016%2fj.mencom.2018.03.012&partnerID=40&md5=0e377db9729c5c45b37d8eb520db1911

 

DOI: 10.1016/j.mencom.2018.03.012


 

 

Frumkin, A.E., Yudin, N.V., Suponitsky, K.Y., Sheremetev, A.B.

1-Amino-1-hydroxyamino-2,2-dinitroethene: novel insights in chemistry of FOX-7

(2018) Mendeleev Communications, 28 (2), pp. 135-137. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044135293&doi=10.1016%2fj.mencom.2018.03.007&partnerID=40&md5=a069bd8af39f4be5c84779839d1d1278

 

DOI: 10.1016/j.mencom.2018.03.007


 

 

Matveev, A.L., Krylov, V.B., Emelyanova, L.A., Solovev, A.S., Khlusevich, Y.A., Baykov, I.K., Fontaine, T., Latgé, J.-P., Tikunova, N.V., Nifantiev, N.E.

Novel mouse monoclonal antibodies specifically recognize Aspergillus fumigatus galactomannan

(2018) PLoS ONE, 13 (3), статья № e0193938, . Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85043467382&doi=10.1371%2fjournal.pone.0193938&partnerID=40&md5=ca8e812867bff9995b897d55b24f8934

 

DOI: 10.1371/journal.pone.0193938


 

 

Lyalin, B.V., Sigacheva, V.L., Kokorekin, V.A., Dutova, T.Y., Rodionov, G.M., Petrosyan, V.A.

Oxidative transformation of N-substituted 3-aminopyrazoles to azopyrazoles using electrogenerated bromine as a mediator

(2018) Russian Chemical Bulletin, 67 (3), pp. 510-516.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049354146&doi=10.1007%2fs11172-018-2102-y&partnerID=40&md5=be4c40ebdedea4cbb27f5127fdd51d1d

 

DOI: 10.1007/s11172-018-2102-y


 

 

Veselovsky, V.V., Lozanova, A.V., Isaeva, V.I., Lobova, A.A., Fitch, A.N., Chernyshev, V.V.

Optically active derivatives of terephthalic acid: Four crystal structures from two powder patterns

(2018) Acta Crystallographica Section C: Structural Chemistry, 74, pp. 248-255.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85043365503&doi=10.1107%2fS2053229618001705&partnerID=40&md5=19ef3b66c91818e1a62e48bbf55f0cf7

 

DOI: 10.1107/S2053229618001705


 

 

Chernysheva, N.B., Maksimenko, A.S., Andreyanov, F.A., Kislyi, V.P., Strelenko, Y.A., Khrustalev, V.N., Semenova, M.N., Semenov, V.V.

Regioselective synthesis of 3,4-diaryl-5-unsubstituted isoxazoles, analogues of natural cytostatic combretastatin A4

(2018) European Journal of Medicinal Chemistry, 146, pp. 511-518. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041856515&doi=10.1016%2fj.ejmech.2018.01.070&partnerID=40&md5=fa9c25269f4827c4b7dd550b53a69f9a

 

DOI: 10.1016/j.ejmech.2018.01.070


 

 

Azov, V.A., Egorova, K.S., Seitkalieva, M.M., Kashin, A.S., Ananikov, V.P.

"solvent-in-salt" systems for design of new materials in chemistry, biology and energy research

(2018) Chemical Society Reviews, 47 (4), pp. 1250-1284. Цитировано 8 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042313709&doi=10.1039%2fc7cs00547d&partnerID=40&md5=1ba1786fb671e791902473301fa5bba2

 

DOI: 10.1039/c7cs00547d


 

 

Burueva, D.B., Kovtunov, K.V., Bukhtiyarov, A.V., Barskiy, D.A., Prosvirin, I.P., Mashkovsky, I.S., Baeva, G.N., Bukhtiyarov, V.I., Stakheev, A.Y., Koptyug, I.V.

Selective Single-Site Pd−In Hydrogenation Catalyst for Production of Enhanced Magnetic Resonance Signals using Parahydrogen

(2018) Chemistry - A European Journal, 24 (11), pp. 2547-2553. Цитировано 7 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041099380&doi=10.1002%2fchem.201705644&partnerID=40&md5=905f0ad5f7df49ed3a43a4f3ad1cd156

 

DOI: 10.1002/chem.201705644


 

 

Kuchurov, I.V., Arabadzhi, S.S., Zharkov, M.N., Fershtat, L.L., Zlotin, S.G.

Sustainable Synthesis of Polynitroesters in the Freon Medium and their in Vitro Evaluation as Potential Nitric Oxide Donors

(2018) ACS Sustainable Chemistry and Engineering, 6 (2), pp. 2535-2540.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041485047&doi=10.1021%2facssuschemeng.7b04029&partnerID=40&md5=c6407a39876d9c5ba241648e693fb6ca

 

DOI: 10.1021/acssuschemeng.7b04029


 

 

Supranovich, V.I., Levin, V.V., Struchkova, M.I., Dilman, A.D.

Photocatalytic Reductive Fluoroalkylation of Nitrones

(2018) Organic Letters, 20 (3), pp. 840-843. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041635316&doi=10.1021%2facs.orglett.7b03987&partnerID=40&md5=0ffca4063afb4079c29642ebf2f67c95

 

DOI: 10.1021/acs.orglett.7b03987


 

 

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Borodina, E.Y., Nifantiev, N.E., Usov, A.I.

A highly regular fucan sulfate from the sea cucumber Stichopus horrens

(2018) Carbohydrate Research, 456, pp. 5-9. Цитировано 5 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85037656212&doi=10.1016%2fj.carres.2017.12.001&partnerID=40&md5=30012bb20f8ebd28b812966ca80305d5

 

DOI: 10.1016/j.carres.2017.12.001


 

 

Barsukov, D.V., Subbotina, I.R.

Effect of surface hydration on the photocatalytic activity of oxide catalysts in the CO oxidation

(2018) Russian Chemical Bulletin, 67 (2), pp. 243-251.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046533714&doi=10.1007%2fs11172-018-2065-z&partnerID=40&md5=aaf1b19380b34f071f94c814d1e9a8ee

 

DOI: 10.1007/s11172-018-2065-z


 

 

Novikov, R.A., Borisov, D.D., Tomilov, Y.V.

Lewis acid-mediated reactions of donor-acceptor cyclopropanes with diazo esters

(2018) Russian Chemical Bulletin, 67 (2), pp. 265-273. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046551077&doi=10.1007%2fs11172-018-2069-8&partnerID=40&md5=e09b4e702b6bed53b29e5175b342f2f8

 

DOI: 10.1007/s11172-018-2069-8


 

 

Ustyuzhanina, N.E., Kulakovskaya, E.V., Kulakovskaya, T.V., Menshov, V.M., Dmitrenok, A.S., Shashkov, A.S., Nifantiev, N.E.

Mannan and phosphomannan from Kuraishia capsulata yeast

(2018) Carbohydrate Polymers, 181, pp. 624-632. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85035347786&doi=10.1016%2fj.carbpol.2017.11.103&partnerID=40&md5=b5a500ba5dd2f84331436b506809f5b1

 

DOI: 10.1016/j.carbpol.2017.11.103


 

 

Sedishev, I.P., Zharov, A.A., Levina, I.S., Tyurin, A.Y., Volkova, Y.A., Aksenov, A.N., Kachala, V.V., Tikhonova, T.A., Zavarzin, I.V.

Synthesis of condensed pregnano[17,16-d]triazolines under high pressure

(2018) Russian Chemical Bulletin, 67 (2), pp. 308-312.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046656293&doi=10.1007%2fs11172-018-2075-x&partnerID=40&md5=f82de17aac6889b3d18f599a814b10bb

 

DOI: 10.1007/s11172-018-2075-x


 

 

Knebel, A., Zhou, C., Huang, A., Zhang, J., Kustov, L., Caro, J.

Smart Metal-Organic Frameworks (MOFs): Switching Gas Permeation through MOF Membranes by External Stimuli

(2018) Chemical Engineering and Technology, 41 (2), pp. 224-234. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040717565&doi=10.1002%2fceat.201700635&partnerID=40&md5=3a5ea9099ee5fa9af6b894d1adc6d1b1

 

DOI: 10.1002/ceat.201700635


 

 

Gorbunov, Y.O., Mityanov, V.S., Melekhina, V.G., Krayushkin, M.M.

Synthesis of novel 4H-furo[3,2-c]pyran-4-ones and 4H-furo[3,2-c]chromen-4-ones

(2018) Russian Chemical Bulletin, 67 (2), pp. 304-307. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046542145&doi=10.1007%2fs11172-018-2074-y&partnerID=40&md5=a6e5e3fcae33cd8a4d48e4a4fadf12af

 

DOI: 10.1007/s11172-018-2074-y


 

 

Perepelov, A.V., Chen, T., Senchenkova, S.N., Filatov, A.V., Song, J., Shashkov, A.S., Liu, B., Knirel, Y.A.

Structure and genetics of the O-specific polysaccharide of Escherichia coli O27

(2018) Carbohydrate Research, 456, pp. 1-4.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85036625566&doi=10.1016%2fj.carres.2017.11.016&partnerID=40&md5=dec5c2ed51ad4a4c89de1ac0fdcc2378

 

DOI: 10.1016/j.carres.2017.11.016


 

 

Root, N.V., Kultin, D.Y., Kustov, L.M., Kudryavtsev, I.K., Lebedeva, O.K.

Erratum to: Effect of the conditions of anodizing on the morphology of nanotitania (Russian Journal of Physical Chemistry A, (2017), 91, 2, (213-216), 10.1134/S0036024417020248)

(2018) Russian Journal of Physical Chemistry A, 92 (2), p. 395.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85043238343&doi=10.1134%2fS0036024418150013&partnerID=40&md5=3303ab9b4957a4b317272c977294bd69

 

DOI: 10.1134/S0036024418150013


 

 

Likhosherstov, L.M., Novikova, O.S., Kolotyrkina, N.G., Berezin, B.B., Piskarev, V.E.

A new method for the synthesis of aldehyde-spacered oligosaccharides by oxidation of l-tartaric acid derivative

(2018) Russian Chemical Bulletin, 67 (2), pp. 371-376.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046698153&doi=10.1007%2fs11172-018-2083-x&partnerID=40&md5=93f5b8037cd4cd065a850bf924cc9c05

 

DOI: 10.1007/s11172-018-2083-x


 

 

Sanin, I.A., Zubarev, A.A., Rudenko, A.Y., Rodinovskaya, L.A., Batuev, E.A., Shestopalov, A.M.

New quinoline- and isoquinoline-based multicomponent methods for the synthesis of 1,1(3,3)-dicyanotetrahydrobenzoindolizines

(2018) Russian Chemical Bulletin, 67 (2), pp. 297-303.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046546725&doi=10.1007%2fs11172-018-2073-z&partnerID=40&md5=73bf11d20e6e2dc0b4d64d5e85182136

 

DOI: 10.1007/s11172-018-2073-z


 

 

Panova, M.V., Podvalnyy, N.M., Okun, E.L., Abronina, P.I., Chizhov, A.O., Kononov, L.O.

Arabinofuranose 1,2,5-orthobenzoate as a single precursor of linear α(1 → 5)-linked oligoarabinofuranosides

(2018) Carbohydrate Research, 456, pp. 35-44. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85038240990&doi=10.1016%2fj.carres.2017.11.002&partnerID=40&md5=a6012d7fd29fff45a4cb0d08d6d4d5b6

 

DOI: 10.1016/j.carres.2017.11.002


 

 

Bubnov, Y.N., Spiridonov, Y.Y., Kuznetsov, N.Y.

New growth regulators of corn based on N-mono- and N,N-bis-3-butenyldichloroacetamides

(2018) Russian Chemical Bulletin, 67 (2), pp. 345-358. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85046687243&doi=10.1007%2fs11172-018-2080-0&partnerID=40&md5=ad1f73dfcc8c188b1ac506842bcf4c4d

 

DOI: 10.1007/s11172-018-2080-0


 

 

Zdorovenko, E.L., Kadykova, A.A., Shashkov, A.S., Varbanets, L.D., Bulyhina, T.V., Knirel, Y.A.

Lipopolysaccharides of Pantoea agglomerans 7604 and 8674 with structurally related O-polysaccharide chains: Chemical identification and biological properties

(2018) Carbohydrate Polymers, 181, pp. 386-393.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85032570930&doi=10.1016%2fj.carbpol.2017.10.087&partnerID=40&md5=8a84d52862cd8db7f0c3fe6ecb92849d

 

DOI: 10.1016/j.carbpol.2017.10.087


 

 

Kenyon, J.J., Kasimova, A.A., Shashkov, A.S., Hall, R.M., Knirel, Y.A.

Acinetobacter baumannii isolate BAL_212 from vietnam produces the K57 capsular polysaccharide containing a rarely occurring amino sugar N-acetylviosamine

(2018) Microbiology (United Kingdom), 164 (2), статья № 000598, pp. 217-220. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041820267&doi=10.1099%2fmic.0.000598&partnerID=40&md5=2164b48a6edf21c5a6a0e3f052ae79ee

 

DOI: 10.1099/mic.0.000598


 

 

Kovalishyn, V., Abramenko, N., Kopernyk, I., Charochkina, L., Metelytsia, L., Tetko, I.V., Peijnenburg, W., Kustov, L.

Modelling the toxicity of a large set of metal and metal oxide nanoparticles using the OCHEM platform

(2018) Food and Chemical Toxicology, 112, pp. 507-517. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85027403346&doi=10.1016%2fj.fct.2017.08.008&partnerID=40&md5=fab9df642e8e01740088e54e76680996

 

DOI: 10.1016/j.fct.2017.08.008


 

 

Bityukov, O.V., Vil, V.A., Merkulova, V.M., Nikishin, G.I., Terent'Ev, A.O.

Silica gel mediated oxidative C-O coupling of β-dicarbonyl compounds with malonyl peroxides in solvent-free conditions

(2018) Pure and Applied Chemistry, 90 (1), pp. 7-20. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040950284&doi=10.1515%2fpac-2017-0312&partnerID=40&md5=b994c9e14df0bafe7461a8920898fd1e

 

DOI: 10.1515/pac-2017-0312


 

 

Ledovskaya, M.S., Rodygin, K.S., Ananikov, V.P.

Calcium-mediated one-pot preparation of isoxazoles with deuterium incorporation

(2018) Organic Chemistry Frontiers, 5 (2), pp. 226-231. Цитировано 5 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040918986&doi=10.1039%2fc7qo00705a&partnerID=40&md5=48dcfbde9209aae808ac20ba06767b75

 

DOI: 10.1039/c7qo00705a


 

 

Salikov, R.F., Trainov, K.P., Belousova, I.K., Belyy, A.Y., Fatkullina, U.S., Mulyukova, R.V., Zainullina, L.F., Vakhitova, Y.V., Tomilov, Y.V.

Branching tryptamines as a tool to tune their antiproliferative activity

(2018) European Journal of Medicinal Chemistry, 144, pp. 211-217.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85038812234&doi=10.1016%2fj.ejmech.2017.12.028&partnerID=40&md5=229d644c9d2fa66fe260508f03ed1576

 

DOI: 10.1016/j.ejmech.2017.12.028


 

 

Shirinian, V.Z., Lvov, A.G., Lonshakov, D.V., Yadykov, A.V., Kachala, V.V., Krayushkin, M.M.

Pinacol rearrangement of cyclopent-3-en-1,2-diols: Cyclopentenone formation and interrupting reaction

(2018) Tetrahedron Letters, 59 (3), pp. 243-246.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85037602166&doi=10.1016%2fj.tetlet.2017.12.016&partnerID=40&md5=2a4dff4a1c0c1ce54c86d378d24e7a5f

 

DOI: 10.1016/j.tetlet.2017.12.016


 

 

Rodygin, K.S., Werner, I., Ananikov, V.P.

A Green and Sustainable Route to Carbohydrate Vinyl Ethers for Accessing Bioinspired Materials with a Unique Microspherical Morphology

(2018) ChemSusChem, 11 (1), pp. 292-298. Цитировано 5 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85038111122&doi=10.1002%2fcssc.201701489&partnerID=40&md5=af1dc4cc3b7e8360de17a73664031ca3

 

DOI: 10.1002/cssc.201701489


 

 

Scherbakov, A.M., Komkov, A.V., Komendantova, A.S., Yastrebova, M.A., Andreeva, O.E., Shirinian, V.Z., Hajra, A., Zavarzin, I.V., Volkova, Y.A.

Steroidal pyrimidines and dihydrotriazines as novel classes of anticancer agents against hormone-dependent breast cancer cells

(2018) Frontiers in Pharmacology, 8 (JAN), статья № 979, . Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040441191&doi=10.3389%2ffphar.2017.00979&partnerID=40&md5=c36042f5f069db745292374a5d65dbd7

 

DOI: 10.3389/fphar.2017.00979


 

 

Myannik, K.A., Yarovenko, V.N., Beloglazkina, E.K., Moiseeva, A.A., Krayushkin, M.M.

Novel copper(II), cobalt(II) and nickel(II) complexes with 5-(4-oxo-4H-chromen-3-yl)-4,5-dihydro-1,3,4-thiadiazole-2-carboxamide: Synthesis, structure, spectroscopic studies

(2018) Polyhedron, 139, pp. 208-214. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85034042795&doi=10.1016%2fj.poly.2017.10.027&partnerID=40&md5=82b81c86c1dcb24847d85fd3c416ad4b

 

DOI: 10.1016/j.poly.2017.10.027


 

 

Ashirbaev, S.S., Levin, V.V., Struchkova, M.I., Dilman, A.D.

Copper-Catalyzed Coupling of Acyl Chlorides with gem-Difluorinated Organozinc Reagents via Acyl Dithiocarbamates

(2018) Journal of Organic Chemistry, 83 (1), pp. 478-483. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85037575782&doi=10.1021%2facs.joc.7b02598&partnerID=40&md5=841ee58bb13990a05c478c6e94357e7f

 

DOI: 10.1021/acs.joc.7b02598


 

 

Filatova, E.V., Turova, O.V., Nigmatov, A.G., Zlotin, S.G.

Green asymmetric synthesis of tetrahydroquinolines in carbon dioxide medium promoted by lipophilic bifunctional tertiary amine – squaramide organocatalysts

(2018) Tetrahedron, 74 (1), pp. 157-164.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85036641050&doi=10.1016%2fj.tet.2017.11.057&partnerID=40&md5=4ee4aba3aefeeb466ba3eb6c4ae39ad5

 

DOI: 10.1016/j.tet.2017.11.057 


 

 

Yashunsky, D.V., Karelin, A.A., Tsvetkov, Y.E., Nifantiev, N.E.

Synthesis of 3-aminopropyl β-(1 → 6)-D-glucotetraoside and its biotinylated derivative

(2018) Carbohydrate Research, 455, pp. 18-22. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85034025426&doi=10.1016%2fj.carres.2017.11.001&partnerID=40&md5=2800d5be3b0b07a290e2ca222d643577

 

DOI: 10.1016/j.carres.2017.11.001


 

 

Gerbst, A.G., Vinnitsky, D.Z., Dmitrenok, A.S., Ustyuzhanina, N.E., Nifantiev, N.E.

Сonformational study of persulfated propyl glucuronide

(2018) Carbohydrate Research, 455, pp. 81-85.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85034848531&doi=10.1016%2fj.carres.2017.11.009&partnerID=40&md5=527de43b91c53c6134835236b046ab4d

 

DOI: 10.1016/j.carres.2017.11.009


 

 

Seitkalieva, M.M., Kashin, A.S., Egorova, K.S., Ananikov, V.P.

Ionic Liquids As Tunable Toxicity Storage Media for Sustainable Chemical Waste Management

(2018) ACS Sustainable Chemistry and Engineering, 6 (1), pp. 719-726. Цитировано 7 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040053689&doi=10.1021%2facssuschemeng.7b03036&partnerID=40&md5=d16d2c2a5e07e23d3e2c2af5e5371478

 

DOI: 10.1021/acssuschemeng.7b03036


 

 

Sukhova, E.V., Yashunsky, D.V., Kurbatova, E.A., Tsvetkov, Y.E., Nifantiev, N.E.

Synthesis of a pseudotetrasaccharide corresponding to a repeating unit of the Streptococcus pneumoniae type 6B capsular polysaccharide*

(2018) Journal of Carbohydrate Chemistry, 37 (1), pp. 1-17.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041121223&doi=10.1080%2f07328303.2017.1420797&partnerID=40&md5=f0560c8638e769b0a0db168606eb02c0

 

DOI: 10.1080/07328303.2017.1420797


 

 

Krylov, V.B., Argunov, D.A., Solovev, A.S., Petruk, M.I., Gerbst, A.G., Dmitrenok, A.S., Shashkov, A.S., Latgé, J.-P., Nifantiev, N.E.

Synthesis of oligosaccharides related to galactomannans from: Aspergillus fumigatus and their NMR spectral data

(2018) Organic and Biomolecular Chemistry, 16 (7), pp. 1188-1199. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042091314&doi=10.1039%2fc7ob02734f&partnerID=40&md5=7aed2e725515a424f4e946b78feaa058

 

DOI: 10.1039/c7ob02734f


 

 

Elinson, M.N., Vereshchagin, A.N., Ryzhkov, F.V., Anisina, Y.E.

'Solvent-free' and 'on-solvent' multicomponent reaction of isatins, malononitrile, and bicyclic CH-acids: A fast and efficient way to a medicinally-privileged spiro-oxindole scaffold

(2018) Arkivoc, 2018 (4), .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056868142&doi=10.24820%2fark.5550190.p010.640&partnerID=40&md5=71e6f571ed4fcbe22765111bfef1cb49

 

DOI: 10.24820/ark.5550190.p010.640


 

 

Chizhov, A.O., Gening, M.L., Pinsker, O.A., Yudina, O.N., Tsvetkov, Y.E., Nifantiev, N.E.

Gas-phase fragmentation studies of cyclic oligo-β-(1→6)-D-glucosamines by electrospray ionization mass spectrometry using a hybrid high-resolution mass spectrometer

(2018) Russian Chemical Bulletin, 67 (1), pp. 144-149.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045852240&doi=10.1007%2fs11172-018-2050-6&partnerID=40&md5=1f4a2769b4966cad3d0faee66e5bb793

 

DOI: 10.1007/s11172-018-2050-6


 

 

Nikishin, G.I., Kapustina, N.I., Sokova, L.L., Bityukov, O.V., Terent'ev, A.O.

A H2O2/HBr system-several directions but one choice: oxidation-bromination of secondary alcohols into mono- or dibromo ketones

(2018) RSC Advances, 8 (50), pp. 28632-28636.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052133817&doi=10.1039%2fc8ra04885a&partnerID=40&md5=8f51251d0e7c23275ab4a225f77f143d

 

DOI: 10.1039/c8ra04885a


 

 

Novikov, M.A., Nefedov, O.M.

(2-Fluoroallyl)boronates: New reagents for diastereoselective 2-fluoroallylboration of aldehydes

(2018) Organic and Biomolecular Chemistry, 16 (27), pp. 4963-4967.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049900841&doi=10.1039%2fc8ob01103f&partnerID=40&md5=4f878ddbd7ef1a7b857dab36e9072d65

 

DOI: 10.1039/c8ob01103f


 

 

Kucherenko, A.S., Kostenko, A.A., Zhdankina, G.M., Kuznetsova, O.Y., Zlotin, S.G.

Green asymmetric synthesis of Warfarin and Coumachlor in pure water catalyzed by quinoline-derived 1,2-diamines

(2018) Green Chemistry, 20 (3), pp. 754-759. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041392061&doi=10.1039%2fc7gc03626d&partnerID=40&md5=69dd29a2af7e3469e5745d73d64f5da5

 

DOI: 10.1039/c7gc03626d


 

 

Krylov, I.B., Paveliev, S.A., Shumakova, N.S., Syroeshkin, M.A., Shelimov, B.N., Nikishin, G.I., Terent'Ev, A.O.

Iminoxyl radicals: Vs. tert -butylperoxyl radical in competitive oxidative C-O coupling with β-dicarbonyl compounds. Oxime ether formation prevails over Kharasch peroxidation

(2018) RSC Advances, 8 (11), pp. 5670-5677.

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DOI: 10.1039/c7ra13587d


 

 

Gordeev, P.B., Smirnov, G.A., Nikitin, S.V., Pokhvisneva, G.V., Ternikova, T.V., Luk’yanov, O.A.

Synthesis of N-β-haloethyl derivatives of bis(oxytriazene oxides) bearing the NCH2O fragment

(2018) Russian Chemical Bulletin, 67 (1), pp. 85-94. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045834600&doi=10.1007%2fs11172-018-2041-7&partnerID=40&md5=59317938dfdea596ce07d37c899411f0

 

DOI: 10.1007/s11172-018-2041-7


 

 

Mytareva, A.I., Bokarev, D.A., Krivoruchenko, D.S., Baeva, G.N., Belyankin, A.Y., Stakheev, A.Y.

Improvement of Low-Temperature Activity of FeBeta Monolith Catalyst in NH3-SCR of NOx

(2018) Topics in Catalysis, . Article in Press.

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DOI: 10.1007/s11244-018-1094-z


 

 

Churakov, A.M., Ioffe, S.L., Voronin, A.A., Tartakovsky, V.A.

Reaction of N-alkyl-N′-(trimethylsilyl)carbodiimides with nitrating agents. The synthesis of N-(tert-butyl)-N′-nitrocarbodiimide

(2018) Russian Chemical Bulletin, 67 (1), pp. 56-60.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045852817&doi=10.1007%2fs11172-018-2037-3&partnerID=40&md5=d87c2efcf30cc7b80d3086b329668389

 

DOI: 10.1007/s11172-018-2037-3


 

 

Borisova, I.A., Zubarev, A.A., Rodinovskaya, L.A., Shestopalov, A.M.

Synthesis and properties of aza analogs of merocyanine dyes based on N-substituted 2- and 4-aminopyridinium salts

(2018) Russian Chemical Bulletin, 67 (1), pp. 168-171.

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DOI: 10.1007/s11172-018-2054-2


 

 

Komendantova, A.S., Fakhrutdinov, A.N., Menchikov, L.G., Sukhorukov, A.Y., Zavarzin, I.V., Volkova, Y.A.

Cyclization of β-Chlorovinyl Thiohydrazones into Pyridazines: A Mechanistic Study

(2018) European Journal of Organic Chemistry, . Article in Press.

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DOI: 10.1002/ejoc.201801118


 

 

Kochetkov, S.V., Kucherenko, A.S., Zlotin, S.G.

Asymmetric synthesis of warfarin and its analogs catalyzed by C 2-symmetric squaramide-based primary diamines

(2018) Organic and Biomolecular Chemistry, 16 (35), pp. 6423-6429.

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DOI: 10.1039/c8ob01576g


 

 

Ustyuzhanina, N.E., Fershtat, L.L., Gening, M.L., Nifantiev, N.E., Makhova, N.N.

Antiaggregant activity of water-soluble furoxans

(2018) Mendeleev Communications, 28 (1), pp. 49-51. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041561349&doi=10.1016%2fj.mencom.2018.01.016&partnerID=40&md5=44cbfb6db0f9e5f8edf1afd7653c7bf3

 

DOI: 10.1016/j.mencom.2018.01.016


 

 

Bastrakov, M.A., Starosotnikov, A.M.

(Figure presented.) Pyrrole ring closure reactions in the synthesis of isoindoles (microreview)

(2018) Chemistry of Heterocyclic Compounds, . Article in Press.

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DOI: 10.1007/s10593-018-2371-2


 

 

Myannik, K.A., Beloglazkina, E.K., Moiseeva, A.A., Baryshnikova, T.K., Yarovenko, V.N., Krayushkin, M.M.

Synthesis and electrochemical study of 2-carbamoyl-4,5-dihydro-1,3,4-thiadiazole-containing ligands and their complexes with CuII, CoII and NiII

(2018) Mendeleev Communications, 28 (1), pp. 79-80.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041604734&doi=10.1016%2fj.mencom.2018.01.026&partnerID=40&md5=4e5fdd2ebb9b12c0abc9eb08443a08d4

 

DOI: 10.1016/j.mencom.2018.01.026


 

 

Kravchenko, A.N., Baranov, V.V., Gazieva, G.A.

Synthesis of glycolurils and their analogues

(2018) Russian Chemical Reviews, 87 (1), pp. 89-108. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041601678&doi=10.1070%2fRCR4763&partnerID=40&md5=bf0f9e542d2dbecf87e2809057360700

 

DOI: 10.1070/RCR4763


 

 

Novikov, R.A., Denisov, D.A., Potapov, K.V., Tkachev, Y.V., Shulishov, E.V., Tomilov, Y.V.

Ionic Ga-Complexes of Alkylidene- and Arylmethylidenemalonates and Their Reactions with Acetylenes: An In-Depth Look into the Mechanism of the Occurring Gallium Chemistry

(2018) Journal of the American Chemical Society, . Article in Press.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055091754&doi=10.1021%2fjacs.8b08913&partnerID=40&md5=770ab49dde35df252a32d93a68d179a6

 

DOI: 10.1021/jacs.8b08913


 

 

Marochkin, I.I., Kuznetsov, V.V., Rykov, A.N., Makhova, N.N., Shishkov, I.F.

Molecular structure study of 1,2,3-trimethyldiaziridine by means of gas electron diffraction method

(2018) Structural Chemistry, . Article in Press.

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DOI: 10.1007/s11224-018-1213-2


 

 

Kalenchuk, A.N., Davshan, N.A., Bogdan, V.I., Dunaev, S.F., Kustov, L.M.

Reversible hydrogenation—dehydrogenation reactions of meta-terphenyl on catalysts with various supports

(2018) Russian Chemical Bulletin, 67 (1), pp. 28-32. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045845741&doi=10.1007%2fs11172-018-2032-8&partnerID=40&md5=899655104328c2ae89b9de9360524227

 

DOI: 10.1007/s11172-018-2032-8


 

 

Kuznetsov, N.Y., Tikhov, R.M., Strelkova, T.V., Bubnov, Y.N.

Dimethylamine adducts of allylic triorganoboranes as effective reagents for Petasis-type homoallylation of primary amines with formaldehyde

(2018) Organic and Biomolecular Chemistry, 16 (39), pp. 7115-7119.

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DOI: 10.1039/c8ob02152j


 

 

Bilan, M.I., Klochkova, N.G., Shashkov, A.S., Usov, A.I.

Polysaccharides of Algae 71*. Polysaccharides of the Pacific brown alga Alaria marginata

(2018) Russian Chemical Bulletin, 67 (1), pp. 137-143. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045834527&doi=10.1007%2fs11172-018-2049-z&partnerID=40&md5=083809057e49b655e548796a5e0d0495

 

DOI: 10.1007/s11172-018-2049-z


 

 

Zhmurov, P.A., Ushakov, P.Y., Novikov, R.A., Sukhorukov, A.Y., Ioffe, S.L.

A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides

(2018) Synlett, 29 (14), pp. 1871-1874.

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DOI: 10.1055/s-0037-1610213


 

 

Gorbunov, Y.О., Lichitsky, B.V., Komogortsev, A.N., Mityanov, V.S., Dudinov, A.А., Krayushkin, M.M.

Synthesis of Condensed Furylacetic Acids Based on Multicomponent Condensation of Heterocyclic Enols with Arylglyoxals and Meldrum's Acid

(2018) Chemistry of Heterocyclic Compounds, . Article in Press.

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DOI: 10.1007/s10593-018-2333-8


 

 

Shkineva, T.K., Kormanov, A.V., Boldinova, V.N., Vatsadze, I.A., Dalinger, I.L.

Synthesis of 4,4'-dinitro-1H,1'H-[3,3'-bipyrazole]-5,5'-diamine

(2018) Chemistry of Heterocyclic Compounds, . Article in Press.

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DOI: 10.1007/s10593-018-2336-5


 

 

Kuznetsov, Y.V., Levina, I.S., Scherbakov, A.M., Andreeva, O.E., Fedyushkina, I.V., Dmitrenok, A.S., Shashkov, A.S., Zavarzin, I.V.

New estrogen receptor antagonists. 3,20-Dihydroxy-19-norpregna-1,3,5(10)-trienes: Synthesis, molecular modeling, and biological evaluation

(2018) European Journal of Medicinal Chemistry, 143, pp. 670-682. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85036516315&doi=10.1016%2fj.ejmech.2017.11.042&partnerID=40&md5=03b7f61273a0acda3d909d1cf532a4f0

 

DOI: 10.1016/j.ejmech.2017.11.042


 

 

Starosotnikov, A.M., Nikol’Skiy, V.V., Bastrakov, M.A., Kachala, V.V., Pavlov, A.A., Ugrak, B.I., Shevelev, S.A.

Synthesis of pyrido[2, 3-a]phenoxazines and pyrido[2, 3-a] phenothiazines via Successive ANAr processes

(2018) ChemistrySelect, 3 (4), pp. 1230-1233.

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DOI: 10.1002/slct.201702806


 

 

Dorokhov, V.S., Golovanov, I.S., Tartakovsky, V.A., Sukhorukov, A.Yu., Ioffe, S.L.

Diastereoselective synthesis and profiling of bicyclic imidazolidinone derivatives bearing a difluoromethylated catechol unit as potent phosphodiesterase 4 inhibitors

(2018) Organic and Biomolecular Chemistry, 16 (38), pp. 6900-6908.

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DOI: 10.1039/C8OB01039K


 

 

Kolomeichuk, S.N., Nizhnik, Y.P., Makhova, N.N., Ovchinnikov, I.V.

Cytotoxic and apoptotic activity of nitrofuroxans on lymphoma cells

(2018) Chemistry of Heterocyclic Compounds, 54 (1), pp. 70-75.

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DOI: 10.1007/s10593-018-2232-z


 

 

Tomilov, Y.V., Menchikov, L.G., Novikov, R.A., Ivanov, O.A., Trushkov, I.V.

Methods for the synthesis of donor-acceptor cyclopropanes

(2018) Russian Chemical Reviews, 87 (3), pp. 201-250. Цитировано 11 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044955812&doi=10.1070%2fRCR4787&partnerID=40&md5=ec4ebd02e6f3f28d44665382dce9212b

 

DOI: 10.1070/RCR4787


 

 

Konstantinova, L.S., Knyazeva, E.A., Gatilov, Y.V., Zlotin, S.G., Rakitin, O.A.

Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release

(2018) Russian Chemical Bulletin, 67 (1), pp. 95-101. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045841618&doi=10.1007%2fs11172-018-2042-6&partnerID=40&md5=df993aa09a2bb38a24cbf05b69e702a5

 

DOI: 10.1007/s11172-018-2042-6


 

 

Dalinger, I.L., Suponitsky, K.Yu., Shkineva, T.K., Lempert, D.B., Sheremetev, A.B.

Bipyrazole bearing ten nitro groups-a novel highly dense oxidizer for forward-looking rocket propulsions

(2018) Journal of Materials Chemistry A, 6 (30), pp. 14780-14786. Цитировано 4 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051015192&doi=10.1039%2fc8ta05179h&partnerID=40&md5=4886325aa8f43807aae1de55739923bb

 

DOI: 10.1039/c8ta05179h


 

 

Kalenchuk, A.N., Bogdan, V.I., Dunaev, S.F., Kustov, L.M.

Dehydrogenation of polycyclic naphthenes on a Pt/C catalyst for hydrogen storage in liquid organic hydrogen carriers

(2018) Fuel Processing Technology, 169, pp. 94-100. Цитировано 7 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85033579364&doi=10.1016%2fj.fuproc.2017.09.023&partnerID=40&md5=9a77d007508cd4cbe6cd54734f287b86

 

DOI: 10.1016/j.fuproc.2017.09.023


 

 

Fesenko, A.A., Grigoriev, M.S., Shutalev, A.D.

A convenient stereoselective access to novel 1,2,4-triazepan-3-ones/thiones: Via reduction or reductive alkylation of 7-membered cyclic semicarbazones and thiosemicarbazones

(2018) Organic and Biomolecular Chemistry, 16 (43), pp. 8072-8089.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056265261&doi=10.1039%2fc8ob01766b&partnerID=40&md5=55aa2b5277039dbca639dcb20eb33ee4

 

DOI: 10.1039/c8ob01766b


 

 

Guranova, N.I., Varlamov, A.V., Novikov, R.A., Aksenov, A.V., Borisova, T.N., Sorokina, E.A., Voskressensky, L.G.

Reaction of benzyne with 1,2,3,4-tetrahydroisoquinolines as an access to 1H-3-benzazepines

(2018) Mendeleev Communications, 28 (1), pp. 22-24.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041621297&doi=10.1016%2fj.mencom.2018.01.005&partnerID=40&md5=1116beb2fb709ff245b3d281a87181ee

 

DOI: 10.1016/j.mencom.2018.01.005


 

 

Stepanova, E.V., Podvalnyy, N.M., Abronina, P.I., Kononov, L.O.

Length Matters: One Additional Methylene Group in a Reactant is Able to Affect the Reactivity Pattern and Significantly Increase the Product Yield

(2018) Synlett, 29 (15), статья № st-2018-b0212-l, pp. 2043-2045. Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053119868&doi=10.1055%2fs-0037-1610648&partnerID=40&md5=daf2d0e577c11bdefa5a053b6caf8a21

 

DOI: 10.1055/s-0037-1610648


 

 

Yanilkin, V.V., Nasretdinova, G.R., Kokorekin, V.A.

Mediated electrochemical synthesis of metal nanoparticles

(2018) Russian Chemical Reviews, 87 (11), pp. 1080-1110.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056137789&doi=10.1070%2fRCR4827&partnerID=40&md5=53fcc1cfdc413f4c336cf0a81859c084

 

DOI: 10.1070/RCR4827


 

 

Chelysheva, E., Aleshin, S., Polushkina, E., Shmakov, R., Shokhin, I., Chilov, G., Turkina, A.

Breastfeeding in patients with chronic myeloid leukaemia: Case series with measurements of drug concentrations in maternal milk and literature review

(2018) Mediterranean Journal of Hematology and Infectious Diseases, 10 (1), статья № e2018027, . Цитирован(ы) 1 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049244121&doi=10.4084%2fMJHID.2018.027&partnerID=40&md5=42090cd56e6004f4e52a3810d55807ae

 

DOI: 10.4084/MJHID.2018.027


 

 

Glebov, E.M., Ruban, N.V., Pozdnyakov, I.P., Grivin, V.P., Plyusnin, V.F., Lvov, A.G., Zakharov, A.V., Shirinian, V.Z.

Mechanistic Aspects of Photoinduced Rearrangement of 2,3-Diarylcyclopentenone Bearing Benzene and Oxazole Moieties

(2018) Journal of Physical Chemistry A, . Article in Press.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053001403&doi=10.1021%2facs.jpca.8b05212&partnerID=40&md5=2d81a9f98cad3c9c733d44fc23f63420

 

DOI: 10.1021/acs.jpca.8b05212


 

 

Konnov, A.A., Klenov, M.S., Churakov, A.M., Strelenko, Y.A., Dmitrienko, A.O., Puntus, L.N., A. Lyssenko, K., Tartakovsky, V.A.

Synthesis of 1,2,3,4-Tetrazine 1,3-Dioxides Annulated with 1,3 a,4,6 a-Tetraazapentalene Systems

(2018) Asian Journal of Organic Chemistry, . Article in Press.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056595211&doi=10.1002%2fajoc.201800545&partnerID=40&md5=ec53f72473664ca9956d3af651c13702

 

DOI: 10.1002/ajoc.201800545


 

 

Tsymbal, A.V., Levin, V.V., Struchkova, M.I., Kokorekin, V.A., Korlyukov, A.A., Dilman, A.D.

Reductive silylation of gem-difluorinated phosphonium salts

(2018) Journal of Fluorine Chemistry, 205, pp. 58-61. Цитировано 2 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85038847883&doi=10.1016%2fj.jfluchem.2017.11.009&partnerID=40&md5=ebae678a8b27f66fbe3daf36b0d85942

 

DOI: 10.1016/j.jfluchem.2017.11.009


 

 

Shirinyan, V.Z., Markosyan, A.I., Baryshnikova, M.A., Yaminova, L.V., L’vov, A.G., Gabrielyan, S.A.

Synthesis and Antiproliferative Activity Evaluation of Aryl(Hetaryl)Cyclopentenone Analogs of Combretastatin A-4

(2018) Pharmaceutical Chemistry Journal, 51 (10), pp. 867-872.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041128647&doi=10.1007%2fs11094-018-1706-8&partnerID=40&md5=f05ed82e43b46fe556b08be6ae63a1d7

 

DOI: 10.1007/s11094-018-1706-8


 

 

Deriabin, K.V., Yaremenko, I.A., Chislov, M.V., Fleury, F., Terent'Ev, A.O., Islamova, R.M.

Similar nature leads to improved properties: Cyclic organosilicon triperoxides as promising curing agents for liquid polysiloxanes

(2018) New Journal of Chemistry, 42 (18), pp. 15006-15013.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053723874&doi=10.1039%2fc8nj02499e&partnerID=40&md5=ca369d621ba160cf63deb1186249083e

 

DOI: 10.1039/c8nj02499e


 

 

Dalinger, I.L., Serushkina, O.V., Muravyev, N.V., Meerov, D.B., Miroshnichenko, E.A., Kon'Kova, T.S., Suponitsky, K.Y., Vener, M.V., Sheremetev, A.B.

Azasydnone-novel "green" building block for designing high energetic compounds

(2018) Journal of Materials Chemistry A, 6 (38), pp. 18669-18676.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054371773&doi=10.1039%2fc8ta06895j&partnerID=40&md5=26f996e4c0630866ef46efa4ec8eed5c

 

DOI: 10.1039/c8ta06895j


 

 

Minyaev, M.E., Roitershtein, D.M., Vinogradov, A.A., Ananyev, I.V., Nifant'Ev, I.E.

(2 R,3 R)-1,4-Dioxa-spiro-[4.4]nonane-2,3-di-carb-oxy-lic and (2 R,3 R)-1,4-dioxa-spiro-[4.5]decane-2,3-di-carb-oxy-lic acids

(2018) Acta Crystallographica Section E: Crystallographic Communications, 74, pp. 1058-1062.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051145574&doi=10.1107%2fS2056989018009593&partnerID=40&md5=64a323f83d48fb44355ef2049fb9a456

 

DOI: 10.1107/S2056989018009593


 

 

Rakitin, O.A., Zibarev, A.V.

Synthesis and Applications of 5-Membered Chalcogen-Nitrogen π-Heterocycles with Three Heteroatoms

(2018) Asian Journal of Organic Chemistry, . Article in Press.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056153516&doi=10.1002%2fajoc.201800536&partnerID=40&md5=be6414c5af284093a9f77e2db673a647

 

DOI: 10.1002/ajoc.201800536


 

 

Konstantinova, L.S., Baranovsky, I.V., Strunyasheva, V.V., Kalogirou, A.S., Popov, V.V., Lyssenko, K.A., Koutentis, P.A., Rakitin, O.A.

The Conversion of 5,5-Bi(1,2,3-dithiazolylidenes) into Isothiazolo[5,4-d]isothiazoles

(2018) Molecules, 23 (6), статья № 1257, .

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047992957&doi=10.3390%2fmolecules23061257&partnerID=40&md5=321eb6df73151f3bfe4c2713f58aeef8

 

DOI: 10.3390/molecules23061257


 

 

Stepanov, A.V., Mel'nik, K.E., Isaeva, V.I., Kapustin, G.I., Chernyshev, V.V., Veselovsky, V.V.

The Henry reaction catalyzed by zeolitic imidazolate framework ZIF-8

(2018) Mendeleev Communications, 28 (1), pp. 88-90.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041588065&doi=10.1016%2fj.mencom.2018.01.030&partnerID=40&md5=845efead402422700e1bd9db0ac3f24c

 

DOI: 10.1016/j.mencom.2018.01.030


 

 

Shuku, Y., Hirai, Y., Semenov, N.A., Kadilenko, E., Gritsan, N.P., Zibarev, A.V., Rakitin, O.A., Awaga, K.

3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(i) and [1,2,5]thiadiazolo[3,4-: C] [1,2,5]thiadiazolidyl

(2018) Dalton Transactions, 47 (29), pp. 9897-9902. Цитировано 3 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85050818654&doi=10.1039%2fc8dt02214c&partnerID=40&md5=a66bfad4ab0c222ba9df302bf6e07007

 

DOI: 10.1039/c8dt02214c


 

 

Roitershtein, D.M., Minashina, K.I., Minyaev, M.E., Ananyev, I.V., Lyssenko, K.A., Tavtorkin, A.N., Nifant’Ev, I.E.

Different coordination modes of trans-2-{[(2-methoxyphenyl) imino]methyl}phenoxide in rare-earth complexes: Influence of the metal cation radius and the number of ligands on steric congestion and ligand coordination modes

(2018) Acta Crystallographica Section C: Structural Chemistry, 74, pp. 1105-1115.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054441337&doi=10.1107%2fS2053229618012421&partnerID=40&md5=eba532153846c2e774aeef0beaa6963a

 

DOI: 10.1107/S2053229618012421


 

 

Abakumov, G.A., Piskunov, A.V., Cherkasov, V.K., Fedushkin, I.L., Ananikov, V.P., Eremin, D.B., Gordeev, E.G., Beletskaya, I.P., Averin, A.D., Bochkarev, M.N., Trifonov, A.A., Dzhemilev, U.M., D'Yakonov, V.A., Egorov, M.P., Vereshchagin, A.N., Syroeshkin, M.A., Jouikov, V.V., Muzafarov, A.M., Anisimov, A.A., Arzumanyan, A.V., Kononevich, Y.N., Temnikov, M.N., Sinyashin, O.G., Budnikova, Y.H., Burilov, A.R., Karasik, A.A., Mironov, V.F., Storozhenko, P.A., Shcherbakova, G.I., Trofimov, B.A., Amosova, S.V., Gusarova, N.K., Potapov, V.A., Shur, V.B., Burlakov, V.V., Bogdanov, V.S., Andreev, M.V.

Organoelement chemistry: Promising growth areas and challenges

(2018) Russian Chemical Reviews, 87 (5), pp. 393-507. Цитировано 5 раз.

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85048048345&doi=10.1070%2fRCR4795&partnerID=40&md5=62fbbcbe2939bd89f488c69eacd3b48e

 

DOI: 10.1070/RCR4795


 

 
 

Конференции, проводимые институтом:

23-25 октября 2019 года

ВСЕРОССИЙСКАЯ КОНФЕРЕНЦИЯ «ХИМИЯ НИТРОСОЕДИНЕНИЙ И РОДСТВЕННЫХ АЗОТ-КИСЛОРОДНЫХ СИСТЕМ» (АКС-2019)

15 - 20 сентября 2019 года

Международная конференция "Катализ и органический синтез" (ICCOS-2019)

19 - 21 июня 2019 года

Второй Российско-французский семинар по химии гипер- и гипокоординированных соединений и интермедиатов элементов 14-й группы Периодической системы

с 13 по 17 мая 2019 г

Всероссийская конференция «Взаимосвязь ионных и ковалентных взаимодействий в дизайне молекулярных и наноразмерных химических систем» (ChemSci-2019)

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Важные события:

Поздравляем сотрудника ИОХ РАН Валентина Ананикова с избранием членом Европейской академии наук (Academia Europaea) Европейская академия наук (Academia Europaea) была основана в 1988 году и объединяет около четырех тысяч признанных специалистов в области математики, медицины, естественных наук, а также гуманитарных наук, права, экономических, социальных и политических наук из большинства стран Европы. В её состав также входят европейские ученые, проживающие в других регионах мира. В настоящее время в составе академии семьдесят два Нобелевских лауреата, причем многие из них были избраны в академию до получения премии.
Этой осенью в Институте органической химии им. Н.Д.Зелинского (ИОХ) РАН прошла Международная конференция ChemTrends – 2018, посвященная современным тенденциям развития химии. На которой были подробно представлены результаты пятилетней работы исследователей ИОХ РАН по масштабной программе “Органические и гибридные молекулярные системы для критических технологий в интересах национальной безопасности и устойчивого развития”
Работа молодых ученых ИОХ РАН заняла первое место в конкурсе «Снимай науку!» телеканала «Наука». На международный конкурс было прислано 1552 заявки из 110 городов из семи стран. Первое место во всех номинациях по результатам интернет-голосования и приз победителя по решению жюри получил видеоролик «Вера, Надежда, Наука», автором которого является Наталия Шубина из лаборатории Металлокомплексных и наноразмерных катализаторов.
Конференция ChemTrends-2018 собрала ученых из России, США, Великобритании, Франции, Норвегии, Ирландии, Германии и других стран. Более тридцати приглашенных докладов высветили современные тенденции химической науки. На конференции представлены результаты проекта по исследованию органических и гибридных молекулярных систем, полученные в рамках Гранта РНФ на реализацию комплексных научных программ организаций.
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