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Публикации за 2017 год

 

Kenyon, J.J., Shashkov, A.S., Senchenkova, S.N., Shneider, M.M., Liu, B., Popova, A.V., Arbatsky, N.P., Miroshnikov, K.A., Wang, L., Knirel, Y.A., Hall, R.M.
Acinetobacter baumannii K11 and K83 capsular polysaccharides have the same 6-deoxy-L-talose-containing pentasaccharide K units but different linkages between the K units
(2017) International Journal of Biological Macromolecules, 103, pp. 648-655. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019633409&doi=10.1016%2fj.ijbiomac.2017.05.082&partnerID=40&md5=42007f35366cf8722e542e562b591e49

DOI: 10.1016/j.ijbiomac.2017.05.082

Sigida, E.N., Fedonenko, Y.P., Shashkov, A.S., Zdorovenko, E.L., Ignatov, V.V., Knirel, Y.A.
Structural studies of the O-specific polysaccharide from detergent degrading bacteria Pseudomonas putida TSh-18
(2017) Carbohydrate Research, 448, pp. 1-5. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019860162&doi=10.1016%2fj.carres.2017.05.013&partnerID=40&md5=b6f2e66d9ad5b8903c18659e525dcf43

DOI: 10.1016/j.carres.2017.05.013

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Borodina, E.Y., Stonik, V.A., Nifantiev, N.E., Usov, A.I.
A highly regular fucosylated chondroitin sulfate from the sea cucumber Massinium magnum: Structure and effects on coagulation
(2017) Carbohydrate Polymers, 167, pp. 20-26. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015403404&doi=10.1016%2fj.carbpol.2017.02.101&partnerID=40&md5=1b7627e557728a1b80422f5122fb5f6d

DOI: 10.1016/j.carbpol.2017.02.101

Zheng, H., Shashkov, A.S., Xiong, Y., Naumenko, O.I., Wang, H., Senchenkova, S.N., Wang, J., Knirel, Y.A.
Structure and gene cluster of the O-antigen of Escherichia albertii O1 resembling the O-antigen of Pseudomonas aeruginosa O5
(2017) Carbohydrate Research, 446-447, pp. 28-31. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018783685&doi=10.1016%2fj.carres.2017.04.024&partnerID=40&md5=35b48f67819842ff56e1ef767c513c4f

DOI: 10.1016/j.carres.2017.04.024

Baranov, V.V., Antonova, M.M., Karnoukhova, V.A., Kravchenko, A.N.
Unexpected reductive transformation of 1-substituted 5-hydroxy-4,5-diphenyl-1H-imidazol-2(5H)-ones and their cyclic analogs by the reaction with thiourea and hydrochloric acid
(2017) Tetrahedron Letters, 58 (23), pp. 2203-2205. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018430228&doi=10.1016%2fj.tetlet.2017.04.061&partnerID=40&md5=e55f9023e508c89ff04a702cfc0cc3a7

DOI: 10.1016/j.tetlet.2017.04.061

Sizova, O.V., Kondakova, A.N., Shashkov, A.S., Knirel, Y.A., Shaikhutdinova, R.Z., Ivanov, S.A., Platonov, M.E., Hurst, M.R.H., Dentovskaya, S.V.
Structure and gene cluster of a tyvelose-containing O-polysaccharide of an entomopathogenic bacterium Yersinia entomophaga MH96T related to Yersinia pseudotuberculosis
(2017) Carbohydrate Research, 445, pp. 93-97. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018330470&doi=10.1016%2fj.carres.2017.04.013&partnerID=40&md5=4b8b2f897efc606b33676948bd1a853c

DOI: 10.1016/j.carres.2017.04.013

Mendkovich, A.S., Syroeshkin, M.A., Nasybullina, D.V., Mikhailov, M.N., Gultyai, V.P., Rusakov, A.I.
Electroreduction mechanism of N-phenylhydroxylamines in aprotic solvents: N-(2-nitrophenyl)- and N-(3-nitrophenyl)hydroxylamines
(2017) Electrochimica Acta, 238, pp. 9-20. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017470338&doi=10.1016%2fj.electacta.2017.03.174&partnerID=40&md5=f0e199fd849e61540987d00b53324c3a

DOI: 10.1016/j.electacta.2017.03.174

Chizhkov, V.P., Boitsov, V.N.
Method for performing a single act of the reversible separation of ideal solution components
(2017) Russian Journal of Physical Chemistry A, 91 (6), pp. 1127-1131. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019660585&doi=10.1134%2fS0036024417060073&partnerID=40&md5=7c1691f7bf2c8ce18e7f7750446d6ff9

DOI: 10.1134/S0036024417060073

Zdorovenko, E.L., Kadykova, A.A., Shashkov, A.S., Varbanets, L.D., Bulyhina, T.V., Knirel, Y.A.
Lipopolysaccharide of Pantoea agglomerans 7969: Chemical identification, function and biological activity
(2017) Carbohydrate Polymers, 165, pp. 351-358. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013847641&doi=10.1016%2fj.carbpol.2017.02.053&partnerID=40&md5=093db09d3abf1f4ba763b6bf272bdc38

DOI: 10.1016/j.carbpol.2017.02.053

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Shashkov, A.S., Nifantiev, N.E., Usov, A.I.
The structure of a fucosylated chondroitin sulfate from the sea cucumber Cucumaria frondosa
(2017) Carbohydrate Polymers, 165, pp. 7-12. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85012307846&doi=10.1016%2fj.carbpol.2017.02.003&partnerID=40&md5=af5315b1338389676126d6a3e4b051fd

DOI: 10.1016/j.carbpol.2017.02.003

Shvetsova, S.V., Shabalin, K.A., Bobrov, K.S., Ivanen, D.R., Ustyuzhanina, N.E., Krylov, V.B., Nifantiev, N.E., Naryzhny, S.N., Zgoda, V.G., Eneyskaya, E.V., Kulminskaya, A.A.
Corrigendum to “Characterization of a new α-L-fucosidase isolated from Fusarium proliferatum LE1 that is regioselective to α-(1 → 4)-L-fucosidic linkage in the hydrolysis of α-L-fucobiosides” [Biochimie (2017) 132C (54–65)] (S0300908416303029) (10.1016/j.biochi.2016.10.014)
(2017) Biochimie, 137, p. 198. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018899144&doi=10.1016%2fj.biochi.2017.04.007&partnerID=40&md5=c6e162583a61b1d5dcf12b5dd03029b4

DOI: 10.1016/j.biochi.2017.04.007

Egorova, K.S., Gordeev, E.G., Ananikov, V.P.
Biological Activity of Ionic Liquids and Their Application in Pharmaceutics and Medicine
(2017) Chemical Reviews, 117 (10), pp. 7132-7189. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017398702&doi=10.1021%2facs.chemrev.6b00562&partnerID=40&md5=a22814c48c489f59f30f601ab8d10558

DOI: 10.1021/acs.chemrev.6b00562

Volkova, Y., Gevorgyan, V.
Synthesis of functionalyzed imidazo[1,2-a]pyridines via domino A3-coupling/cycloisomerization approach
(2017) Chemistry of Heterocyclic Compounds, pp. 1-4. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019172895&doi=10.1007%2fs10593-017-2066-0&partnerID=40&md5=bd18b7caa30393d0a37a683b7f5673af

DOI: 10.1007/s10593-017-2066-0

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Nifantiev, N.E., Usov, A.I.
Two fucosylated chondroitin sulfates from the sea cucumber Eupentacta fraudatrix
(2017) Carbohydrate Polymers, 164, pp. 8-12. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010818030&doi=10.1016%2fj.carbpol.2017.01.034&partnerID=40&md5=f912e930652f0aa6777ceff0928d64dc

DOI: 10.1016/j.carbpol.2017.01.034

Ivanov, S.M., Mironovich, L.M., Rodinovskaya, L.A., Shestopalov, A.M.
The first stable examples of compounds containing both diazonium and acyl azide, and synthesis of a new pyrazino[2′,3′:3,4]pyrazolo[5,1-c][1,2,4]triazin-4(6H)-one heterocyclic system
(2017) Tetrahedron Letters, 58 (19), pp. 1851-1853. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017101688&doi=10.1016%2fj.tetlet.2017.03.083&partnerID=40&md5=11aca579be98eb485b23a17ffceb1389

DOI: 10.1016/j.tetlet.2017.03.083

Fershtat, L.L., Makhova, N.N.
Molecular Hybridization Tools in the Development of Furoxan-Based NO-Donor Prodrugs
(2017) ChemMedChem, 12 (9), pp. 622-638. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017469077&doi=10.1002%2fcmdc.201700113&partnerID=40&md5=c9b61c6704d64f4c78e13a9a6e0c007b

DOI: 10.1002/cmdc.201700113

Medvedev, M.G., Bushmarinov, I.S., Sun, J., Perdew, J.P., Lyssenko, K.A.
Response to comment on "Density functional theory is straying from the path toward the exact functional"
(2017) Science, 356 (6337), p. 496c. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018422764&doi=10.1126%2fscience.aam9550&partnerID=40&md5=a8fb526cbab47697e90fd2cdf719f16f

DOI: 10.1126/science.aam9550

Gerasimchuk, V.V., Kucherenko, A.S., Fakhrutdinov, A.N., Medvedev, M.G., Nelyubina, Y.V., Zlotin, S.G.
Towards Sustainable Amino Acid Derived Organocatalysts for Asymmetric syn-Aldol Reactions
(2017) European Journal of Organic Chemistry, 2017 (17), pp. 2540-2544. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019039251&doi=10.1002%2fejoc.201700166&partnerID=40&md5=c7d45889b73e9037fd3964a5042ed782

DOI: 10.1002/ejoc.201700166

Badikova, A.D., Kudasheva, F.K., Tsadkin, M.A., Mortikov, E.S., Yalalova, R.A.
Complex Technological Solution for Recycling of Spent Sulfuric Acid from Alkylation of Isobutane by Olefins
(2017) Chemistry and Technology of Fuels and Oils, pp. 1-9. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018364328&doi=10.1007%2fs10553-017-0778-6&partnerID=40&md5=09fa20aae55eac96ee88e83424dc5650

DOI: 10.1007/s10553-017-0778-6

Zaitsev, K.V., Kuchuk, E.A., Churakov, A.V., Navasardyan, M.A., Egorov, M.P., Zaitseva, G.S., Karlov, S.S.
Synthesis and structural characterization of low-valent group 14 metal complexes based on aminobisphenol ligands
(2017) Inorganica Chimica Acta, 461, pp. 213-220. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016720615&doi=10.1016%2fj.ica.2017.02.024&partnerID=40&md5=f623f77ba6ffcc893a091ebb71a3948a

DOI: 10.1016/j.ica.2017.02.024

Medved'ko, A.V., Ivanov, V.K., Kiskin, M.A., Sadovnikov, A.A., Apostolova, E.S., Grinberg, V.A., Emets, V.V., Chizhov, A.O., Nikitin, O.M., Magdesieva, T.V., Kozyukhin, S.A.
The design and synthesis of thiophene-based ruthenium(II) complexes as promising sensitizers for dye-sensitized solar cells
(2017) Dyes and Pigments, 140, pp. 169-178. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010382995&doi=10.1016%2fj.dyepig.2017.01.030&partnerID=40&md5=bf5dec74b423b61c4afc7c1c11229d38

DOI: 10.1016/j.dyepig.2017.01.030

Asfandiarov, N.L., Pshenichnyuk, S.A., Vorob’ev, A.S., Nafikova, E.P., Mavrodiev, V.K., Furlei, I.I., Dokichev, V.A., Platonov, D.N., Belyy, A.Y.
Estimating electron affinity from the lifetime of negative molecular ions: Cycloheptatriene derivatives
(2017) Russian Journal of Physical Chemistry A, 91 (5), pp. 915-920. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018485011&doi=10.1134%2fS0036024417050041&partnerID=40&md5=aa280cc706732cdc6114075fa424518a

DOI: 10.1134/S0036024417050041

dos Passos Gomes, G., Yaremenko, I.A., Radulov, P.S., Novikov, R.A., Chernyshev, V.V., Korlyukov, A.A., Nikishin, G.I., Alabugin, I.V., Terent'ev, A.O.
Stereoelectronic Control in the Ozone-Free Synthesis of Ozonides
(2017) Angewandte Chemie - International Edition, 56 (18), pp. 4955-4959. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017375017&doi=10.1002%2fanie.201610699&partnerID=40&md5=efb363f1ae5d35e77f4570f109091504

DOI: 10.1002/anie.201610699

Gazieva, G.A., Karpova, T.B., Nechaeva, T.V., Nelyubina, Y.V., Zanin, I.E., Kravchenko, A.N.
Synthesis of N-{5-Oxo-2-thioxo(2,5-dithioxo)hexahydroimidazo-[4,5-d]imidazol-1(2H)-yl}formamides
(2017) Synlett, 28 (7), art. no. st-2016-d0667-l, pp. 858-862. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009357374&doi=10.1055%2fs-0036-1588388&partnerID=40&md5=c152e3aa9f51400fec419b37874f14cf

DOI: 10.1055/s-0036-1588388

Samoilova, N.A., Krayukhina, M.A., Babushkina, T.A., Yamskov, I.A., Likhosherstov, L.M., Piskarev, V.E.
Silver- and gold-labeled colloidal and crosslinked glycopolymers based on glycyl glycosynthons and maleic anhydride copolymers for lectin binding
(2017) Journal of Applied Polymer Science, 134 (16), art. no. 44718, . Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009816064&doi=10.1002%2fapp.44718&partnerID=40&md5=df060bc659821ae3c4988a3f87dc31ff

DOI: 10.1002/app.44718

Chen, C., Hou, X., Utkina, N., Danilov, L., Zhou, D., Torgov, V., Veselovsky, V., Liu, B., Feng, L.
Identification and biochemical characterization of a novel α-1,3-mannosyltransferase WfcD from Escherichia coli O141
(2017) Carbohydrate Research, 443-444, pp. 78-86. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017256670&doi=10.1016%2fj.carres.2017.04.003&partnerID=40&md5=b2dbfad233df9eb1ba12a125838da8e0

DOI: 10.1016/j.carres.2017.04.003

Abronina, P.I., Zinin, A.I., Malysheva, N.N., Stepanova, E.V., Chizhov, A.O., Torgov, V.I., Kononov, L.O.
A Novel Glycosyl Donor with a Triisopropylsilyl Nonparticipating Group in Benzyl-Free Stereoselective 1,2-cis-Galactosylation
(2017) Synlett, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019158185&doi=10.1055%2fs-0036-1589028&partnerID=40&md5=62af308c20232abf2e359af881fb4d0c

DOI: 10.1055/s-0036-1589028

Tukhvatshin, R.S., Kucherenko, A.S., Nelyubina, Y.V., Zlotin, S.G.
Tertiary Amine-Derived Ionic Liquid-Supported Squaramide as a Recyclable Organocatalyst for Noncovalent "on Water" Catalysis
(2017) ACS Catalysis, 7 (4), pp. 2981-2989. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019688200&doi=10.1021%2facscatal.7b00562&partnerID=40&md5=9517a922b1279a648db5b18ffb0b2e31

DOI: 10.1021/acscatal.7b00562

Zhmurov, P.A., Khoroshutina, Y.A., Novikov, R.A., Golovanov, I.S., Sukhorukov, A.Y., Ioffe, S.L.
Divergent Reactivity of In Situ Generated Metal Azides: Reaction with N,N-Bis(oxy)enamines as a Case Study
(2017) Chemistry - A European Journal, 23 (19), pp. 4570-4578. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85012050440&doi=10.1002%2fchem.201605390&partnerID=40&md5=4adb829c9099994d9241424fa46e4d6a

DOI: 10.1002/chem.201605390

Zhmurov, P.A., Khoroshutina, Y.A., Novikov, R.A., Golovanov, I.S., Sukhorukov, A.Y., Ioffe, S.L.
Divergent Reactivity of In Situ Generated Metal Azides: Reaction with N,N-Bis(oxy)enamines as a Case Study
(2017) Chemistry - A European Journal, 23 (19), p. 4466. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017173007&doi=10.1002%2fchem.201700193&partnerID=40&md5=1214975bfe065f90c4848e2694eb0767

DOI: 10.1002/chem.201700193

Kasimova, A.A., Shneider, M.M., Arbatsky, N.P., Popova, A.V., Shashkov, A.S., Miroshnikov, K.A., Balaji, V., Biswas, I., Knirel, Y.A.
Structure and gene cluster of the K93 capsular polysaccharide of Acinetobacter baumannii B11911 containing 5-N-Acetyl-7-N-[(R)-3-hydroxybutanoyl]pseudaminic acid
(2017) Biochemistry (Moscow), 82 (4), pp. 483-489. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017513953&doi=10.1134%2fS0006297917040101&partnerID=40&md5=4c86aed9e4b4cf341bda7eb7cd8d0108

DOI: 10.1134/S0006297917040101

Baranov, V.V., Antonova, M.M., Nelyubina, Y.V., Kolotyrkina, N.G., Kravchenko, A.N.
New Method for the Synthesis of 1-Substituted (3a,6a)-Diaryl­glycolurils
(2017) Synlett, 28 (6), art. no. st-2016-d0733-l, pp. 669-672. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009380828&doi=10.1055%2fs-0036-1588932&partnerID=40&md5=31e2d80b70005bd7bc1510bd2eb14e7f

DOI: 10.1055/s-0036-1588932

Elinson, M.N., Vereshchagin, A.N., Korshunov, A.D., Ryzhkov, F.V., Egorov, M.P.
Stereoselective cascade assembling of benzylidenecyanoacetates and 1,3-dimethylbarbituric acid into (1R∗,2S∗)-1-cyano-5,7-dialkyl-4,6,8-trioxo-2-aryl-5,7-diazaspiro[2.5]octane-1-carboxylates
(2017) Heterocyclic Communications, 23 (2), pp. 85-90. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017288324&doi=10.1515%2fhc-2016-0190&partnerID=40&md5=1f19884b9d908d871cd055097dc00659

DOI: 10.1515/hc-2016-0190

Varizhuk, A., Ischenko, D., Tsvetkov, V., Novikov, R., Kulemin, N., Kaluzhny, D., Vlasenok, M., Naumov, V., Smirnov, I., Pozmogova, G.
The expanding repertoire of G4 DNA structures
(2017) Biochimie, 135, pp. 54-62. Cited 2 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010662216&doi=10.1016%2fj.biochi.2017.01.003&partnerID=40&md5=42a790ff3b57b18936c8be24bcdda13d

DOI: 10.1016/j.biochi.2017.01.003

Borisova, I.A., Zubarev, A.A., Rodinovskaya, L.A., Shestopalov, A.M.
Synthesis and physicochemical properties of merocyanine dyes based on dihydropyridine and fragments of cyanoacetic acid derivatives
(2017) Arkivoc, 2017 (3), pp. 73-86. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017303778&doi=10.3998%2fark.5550190.0018.300&partnerID=40&md5=2876966cc24f25a3fe058ef6721b49cf

DOI: 10.3998/ark.5550190.0018.300

Shleeva, M.O., Trutneva, K.A., Demina, G.R., Zinin, A.I., Sorokoumova, G.M., Laptinskaya, P.K., Shumkova, E.S., Kaprelyants, A.S.
Free trehalose accumulation in dormant Mycobacterium smegmatis cells and its breakdown in early resuscitation phase
(2017) Frontiers in Microbiology, 8 (MAR), art. no. 524, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016608640&doi=10.3389%2ffmicb.2017.00524&partnerID=40&md5=118a83db416fb37ea97f2f794b2d5c8e

DOI: 10.3389/fmicb.2017.00524

Lyalin, B.V., Sigacheva, V.L., Kokorekin, V.A., Petrosyan, V.A.
Oxidative conversion of N-substituted 3-Aminopyrazoles to azopyrazoles using electrogenerated NaOCl as the mediator
(2017) Arkivoc, 2017 (3), pp. 55-62. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017322315&doi=10.3998%2fark.5550190.p010.030&partnerID=40&md5=6b841981bd2a7a9750a9be4fd9350b18

DOI: 10.3998/ark.5550190.p010.030

Baranov, V.V., Antonova, M.M., Karnoukhova, V.A., Kravchenko, A.N.
Unusual formation of imidazooxazolone in the reaction of 1-[(2-Acetylamino)ethyl]imidazolone with KSCN in the presence of AcOH
(2017) Arkivoc, 2017 (3), pp. 63-72. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017295243&doi=10.3998%2fark.5550190.p010.048&partnerID=40&md5=341418f56d5251aede8b1bc18782fbe8

DOI: 10.3998/ark.5550190.p010.048

Medvedev, M.G., Zeifman, A.A., Novikov, F.N., Bushmarinov, I.S., Stroganov, O.V., Titov, I.Yu., Chilov, G.G., Svitanko, I.V.
Quantifying Possible Routes for SpnF-Catalyzed Formal Diels-Alder Cycloaddition
(2017) Journal of the American Chemical Society, 139 (11), pp. 3942-3945. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015881878&doi=10.1021%2fjacs.6b13243&partnerID=40&md5=e30250666997710decc00b5960e97653

DOI: 10.1021/jacs.6b13243

Fedorov, O.V., Struchkova, M.I., Dilman, A.D.
Synthesis of gem-Difluorinated Hydroxypyrrolidines
(2017) Journal of Organic Chemistry, 82 (6), pp. 3270-3275. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015677962&doi=10.1021%2facs.joc.6b03033&partnerID=40&md5=3cde7fc940df5fcd847682d649ac790f

DOI: 10.1021/acs.joc.6b03033

Baranov, M.S., Kaskova, Z.M., Gritсenko, R., Postikova, S.G., Ivashkin, P.E., Kislukhin, A.A., Moskvin, D.I., Mineev, K.S., Arseniev, A.S., Labas, Y.A., Yampolsky, I.V.
Synthesis of Panal Terpenoid Core
(2017) Synlett, 28 (5), art. no. st-2016-b0575-l, pp. 583-588. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996939000&doi=10.1055%2fs-0036-1588104&partnerID=40&md5=404b9a305e60c487ae6a81c77fe38f54

DOI: 10.1055/s-0036-1588104

Shirinian, V.Z., Kavun, A.M., Lvov, A.G., Zavarzin, I.V., Krayushkin, M.M.
Practical and Efficient Synthesis of Polyaryl(hetaryl)-Substituted Cyclohexenones and Salicylates
(2017) Synthesis (Germany), 49 (6), art. no. ss-2016-z0605-op, pp. 1255-1263. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84997161511&doi=10.1055%2fs-0036-1588908&partnerID=40&md5=38ddca3efef0c2c5b6bc273a73095c25

DOI: 10.1055/s-0036-1588908

Novikov, R.A., Tarasova, A.V., Denisov, D.A., Borisov, D.D., Korolev, V.A., Timofeev, V.P., Tomilov, Y.V.
[4 + 2] Annulation of Donor-Acceptor Cyclopropanes with Acetylenes Using 1,2-Zwitterionic Reactivity
(2017) Journal of Organic Chemistry, 82 (5), pp. 2724-2738. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85014513122&doi=10.1021%2facs.joc.7b00209&partnerID=40&md5=ab924e9b596e664987ba6a35329d1055

DOI: 10.1021/acs.joc.7b00209

Kenyon, J.J., Kasimova, A.A., Shneider, M.M., Shashkov, A.S., Arbatsky, N.P., Popova, A.V., Miroshnikov, K.A., Hall, R.M., Knirel, Y.A.
The KL24 gene cluster and a genomic island encoding a Wzy polymerase contribute genes needed for synthesis of the K24 capsular polysaccharide by the multiply antibiotic resistant Acinetobacter baumannii isolate RCH51
(2017) Microbiology (United Kingdom), 163 (3), pp. 355-363. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017033872&doi=10.1099%2fmic.0.000430&partnerID=40&md5=5ebf08df9e887ecd0af06acf69db1d73

DOI: 10.1099/mic.0.000430

Levin, V.V., Struchkova, M.I., Dilman, A.D.
Coupling of N-acyliminium chlorides with gem-difluorinated organozinc reagents
(2017) Mendeleev Communications, 27 (2), pp. 139-140. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015985169&doi=10.1016%2fj.mencom.2017.03.010&partnerID=40&md5=c848fc864b185ceb4d3648484e8a7591

DOI: 10.1016/j.mencom.2017.03.010

Stakheev, A.Y., Bokarev, D.A., Mytareva, A.I., Janssens, T.V.W., Vennestrøm, P.N.R.
Detailed Study of Cu Migration in the Course of NH<inf>3</inf>-Facilitated Solid-State Ion-Exchange into *BEA Zeolites
(2017) Topics in Catalysis, 60 (3-5), pp. 255-259. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016966749&doi=10.1007%2fs11244-016-0607-x&partnerID=40&md5=ecc59381530632be095b8b952ede2750

DOI: 10.1007/s11244-016-0607-x

Mishanin, I.I., Kalenchuk, A.N., Maslakov, K.I., Lunin, V.V., Koklin, A.E., Finashina, E.D., Bogdan, V.I.
Oxidative dehydrogenation of ethane over a Mo–V–Nb–Te–O mixed-oxide catalyst in a cyclic mode
(2017) Kinetics and Catalysis, 58 (2), pp. 156-160. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017611816&doi=10.1134%2fS0023158417020094&partnerID=40&md5=8776d8910e06f3e340b3e5a0d44845a3

DOI: 10.1134/S0023158417020094

Zharkov, M.N., Kuchurov, I.V., Fomenkov, I.V., Tartakovsky, V.A., Fedyanin, I.V., Zlotin, S.G.
Safe and Convenient Synthesis of Primary N -Nitramines in the Freon Media
(2017) Synthesis (Germany), 49 (5), art. no. ss-2016-t0532-op, pp. 1103-1108. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991280268&doi=10.1055%2fs-0036-1588616&partnerID=40&md5=330b7f2a7df33a73218eaf13decf58d5

DOI: 10.1055/s-0036-1588616

Chizhkov, V.P., Boitsov, V.N.
A generalized theory of chromatography and multistep liquid extraction
(2017) Russian Journal of Physical Chemistry A, 91 (3), pp. 586-594. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85014038955&doi=10.1134%2fS0036024417030074&partnerID=40&md5=eefd4a35566bdb90a4abce38fef351ce

DOI: 10.1134/S0036024417030074

Bruk, L.G., Ustyugov, A.V., Katsman, E.A., Iskhakova, L.D., Oshanina, I.V., Tkachenko, O.P., Kustov, L.M., Temkin, O.N.
Kinetics and mechanism of the low-temperature oxidation of carbon monoxide with oxygen on a PdCl<inf>2</inf>–CuCl<inf>2</inf>/γ-Al<inf>2</inf>O<inf>3</inf> catalyst
(2017) Kinetics and Catalysis, 58 (2), pp. 179-190. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017620264&doi=10.1134%2fS0023158417020033&partnerID=40&md5=325e3734d2aa22190e399f03920caf80

DOI: 10.1134/S0023158417020033

Silchenko, A.S., Ustyuzhanina, N.E., Kusaykin, M.I., Krylov, V.B., Shashkov, A.S., Dmitrenok, A.S., Usoltseva, R.V., Zueva, A.O., Nifantiev, N.E., Zvyagintseva, T.N.
Expression and biochemical characterization and substrate specificity of the fucoidanase from Formosa algae
(2017) Glycobiology, 27 (3), pp. 254-263. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015907449&doi=10.1093%2fglycob%2fcww138&partnerID=40&md5=f17112115ad5621c09e60b510ccbb372

DOI: 10.1093/glycob/cww138

Vostrikov, N.S., Lobko, I.F., Spirikhin, L.V., Vakhitova, Y.V., Pivnitsky, K.K., Miftakhov, M.S.
Side-modified 15-deoxy-Δ12,14-prostaglandin D<inf>2</inf>, precursor of corresponding PGJ<inf>2</inf>. Synthesis from cloprostenol and anticancer activity
(2017) Mendeleev Communications, 27 (2), pp. 125-127. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015977487&doi=10.1016%2fj.mencom.2017.03.005&partnerID=40&md5=2165384f7fda13875ac86724e3292b39

DOI: 10.1016/j.mencom.2017.03.005

Vedenyapina, M.D., Sharifullina, L.R., Kulaishin, S.A., Vedenyapin, A.A., Lapidus, A.L.
Adsorption of 2,4-dichlorophenoxyacetic acid on activated carbon
(2017) Solid Fuel Chemistry, 51 (2), pp. 115-121. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018250187&doi=10.3103%2fS0361521917020100&partnerID=40&md5=0941c5dbf565f6a4d12649ea516e5b9d

DOI: 10.3103/S0361521917020100

Dutov, M.D., Shevelev, S.A., Koshelev, V.N., Aleksanyan, D.R., Serushkina, O.V., Neverova, O.D., Kolvina, E.V., Bobrov, E.S.
Dual reactivity of 1-chloro- and 1-bromo-3,5-dinitrobenzenes in aromatic nucleophilic substitution
(2017) Mendeleev Communications, 27 (2), pp. 160-162. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016062522&doi=10.1016%2fj.mencom.2017.03.018&partnerID=40&md5=25b1c041cba42c3df14ec0c51535f316

DOI: 10.1016/j.mencom.2017.03.018

Prezent, M.A., Daeva, E.D., Baranin, S.V., Zavarzin, I.V.
A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5-a]pyrimidines
(2017) Mendeleev Communications, 27 (2), pp. 169-171. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016012933&doi=10.1016%2fj.mencom.2017.03.021&partnerID=40&md5=e45dc8bec71091d0d7c706a0c91ef508

DOI: 10.1016/j.mencom.2017.03.021

Knyazeva, E.A., Wu, W., Chmovzh, T.N., Robertson, N., Woollins, J.D., Rakitin, O.A.
Dye-sensitized solar cells: Investigation of D-A-π-A organic sensitizers based on [1,2,5]selenadiazolo[3,4-c]pyridine
(2017) Solar Energy, 144, pp. 134-143. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009344276&doi=10.1016%2fj.solener.2017.01.016&partnerID=40&md5=9937a647ff6bf1898021fdf013bac540

DOI: 10.1016/j.solener.2017.01.016

Kuznetsov, V.V., Marochkin, I.I., Goloveshkin, A.S., Makhova, N.N., Shishkov, I.F.
Comparable study of the structure of 1,2-bis(2-acetamidoethyl) diaziridine and 3,3-diethyldiaziridine with structures of related compounds by X-ray diffraction analysis and quantum chemical calculations
(2017) Structural Chemistry, pp. 1-11. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013159203&doi=10.1007%2fs11224-016-0908-5&partnerID=40&md5=6964b6345d899217dea39067f1e63807

DOI: 10.1007/s11224-016-0908-5

Fetisov, E.O., Gloriozov, I.P., Nechaev, M.S., Kahlal, S., Saillard, J.-Y., Oprunenko, Y.F.
Thermally induced inter-ring haptotropic rearrangements in π-complexes of molybdenum with nitrogen containing polyaromatic heterocycles: A DFT study
(2017) Journal of Organometallic Chemistry, 830, pp. 212-218. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85008392741&doi=10.1016%2fj.jorganchem.2016.12.004&partnerID=40&md5=33f0ad8ea91b2dce4fbce6d63221f764

DOI: 10.1016/j.jorganchem.2016.12.004

Lvov, A.G., Kavun, A.M., Kachala, V.V., Nelyubina, Y.V., Metelitsa, A.V., Shirinian, V.Z.
Structural and Spectral Properties of Photochromic Diarylethenes: Size Effect of the Ethene Bridge
(2017) Journal of Organic Chemistry, 82 (3), pp. 1477-1486. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85011650276&doi=10.1021%2facs.joc.6b02665&partnerID=40&md5=28a597acf3e1a85f4b30b335f8ef2e2e

DOI: 10.1021/acs.joc.6b02665

Shesterkina, A.A., Shuvalova, E.V., Kirichenko, O.A., Strelkova, A.A., Nissenbaum, V.D., Kapustin, G.I., Kustov, L.M.
Application of silica-supported Fe–Cu nanoparticles in the selective hydrogenation of p-dinitrobenzene to p-phenylenediamine
(2017) Russian Journal of Physical Chemistry A, 91 (2), pp. 201-204. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013321923&doi=10.1134%2fS0036024417020285&partnerID=40&md5=8c70ba95c7e3a2775b4c594606483b80

DOI: 10.1134/S0036024417020285

Roshchina, T.M., Shoniya, N.K., Tegina, O.Y., Tkachenko, O.P., Kustov, L.M.
Physicochemical properties of the surfaces of silica species
(2017) Russian Journal of Physical Chemistry A, 91 (2), pp. 217-225. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013301354&doi=10.1134%2fS003602441702025X&partnerID=40&md5=c60aa24f3fd6561713dd3e851329a6be

DOI: 10.1134/S003602441702025X

Volkova, Y.A., Chernoburova, E.I., Petrova, A.S., Shtil, A.A., Zavarzin, I.V.
Reactions of hydrazones derived from oxamic acid thiohydrazides
(2017) Phosphorus, Sulfur and Silicon and the Related Elements, 192 (2), pp. 237-240. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009436187&doi=10.1080%2f10426507.2016.1250759&partnerID=40&md5=1430f8907c38995bb04010071b01c60c

DOI: 10.1080/10426507.2016.1250759

Stakheev, A.Y., Kaichev, V.V., Bukhtiyarov, V.I.
Preface
(2017) Topics in Catalysis, 60 (1-2), . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013964533&doi=10.1007%2fs11244-016-0728-2&partnerID=40&md5=6ee7a8106e031229d7414ced8082a20c

DOI: 10.1007/s11244-016-0728-2

Novikov, M.A., Ibatov, Y.A., Volchkov, N.V., Lipkind, M.B., Semenov, S.E., Nefedov, O.M.
Copper-catalyzed ligand free ring-opening amination of gem-fluorohalocyclopropanes – An efficient route toward 2-fluoroallylamines
(2017) Journal of Fluorine Chemistry, 194, pp. 58-72. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009286625&doi=10.1016%2fj.jfluchem.2017.01.001&partnerID=40&md5=d2ec7de2c225eb5b1d4c8c7d61113af5

DOI: 10.1016/j.jfluchem.2017.01.001

Ayt, A.O., Barachevsky, V.A., Duensing, A., Fomicheva, Y.Y., Gagarskiy, S.V., Iglev, H., Kiyko, V.V., Krayushkin, M.M., Sergeev, A.N., Veniaminov, A.V., Zakharov, V.V.
Thresholds for nonlinear recording of fluorescent centers in chromone-doped polymer films
(2017) Optical and Quantum Electronics, 49 (2), art. no. 72, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010735747&doi=10.1007%2fs11082-017-0900-3&partnerID=40&md5=ecc1ef0e039a1c7b164713e1db1ea80f

DOI: 10.1007/s11082-017-0900-3

Novakov, I.A., Yablokov, A.S., Navrotskii, M.B., Mkrtchyan, A.S., Vernigora, A.A., Babushkin, A.S., Kachala, V.V., Ruchko, E.A.
Synthesis of 3-oxoesters and functional derivatives of pyrimidin-4(3Н)-one based on 1-(2,6-dihalophenyl)cyclopropan-1-carboxylic acids
(2017) Russian Journal of General Chemistry, 87 (2), pp. 224-230. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017255727&doi=10.1134%2fS1070363217020128&partnerID=40&md5=4482907644a152071c137b21b641be43

DOI: 10.1134/S1070363217020128

Barsegyan, Y.A., Baranov, V.V., Kravchenko, A.N.
Glycolurils in the synthesis of fused polyheterocyclic compounds
(2017) Chemistry of Heterocyclic Compounds, 53 (2), pp. 116-122. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015235415&doi=10.1007%2fs10593-017-2029-5&partnerID=40&md5=02388fcbab235a3f0b78e7522ce559eb

DOI: 10.1007/s10593-017-2029-5

Lebedeva, O., Kultin, D., Kudryavtsev, I., Root, N., Kustov, L.
The role of initial hexagonal self-ordering in anodic nanotube growth in ionic liquid
(2017) Electrochemistry Communications, 75, pp. 78-81. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009060617&doi=10.1016%2fj.elecom.2017.01.005&partnerID=40&md5=44800c6c814e058f39415d4a1cde8af6

DOI: 10.1016/j.elecom.2017.01.005

Polikarpova, A.V., Maslakova, A.A., Levina, I.S., Kulikova, L.E., Kuznetsov, Y.V., Guseva, A.A., Shchelkunova, T.A., Zavarzin, I.V., Smirnova, O.V.
Selection of progesterone derivatives specific to membrane progesterone receptors
(2017) Biochemistry (Moscow), 82 (2), pp. 140-148. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013159243&doi=10.1134%2fS0006297917020055&partnerID=40&md5=aec0a4f8b2cf5be9802d2b868f26d168

DOI: 10.1134/S0006297917020055

Knirel, Y.A., Guo, X., Senchenkova, S.N., Perepelov, A.V., Liu, B., Shashkov, A.S.
Structures and gene clusters of the O-specific polysaccharides of the lipopolysaccharides of Escherichia coli O69 and O146 containing glycolactilic acids: ether conjugates of d-GlcNAc and d-Glc with (R)- and (S)-lactic acid
(2017) Glycoconjugate Journal, 34 (1), pp. 71-84. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988424251&doi=10.1007%2fs10719-016-9730-y&partnerID=40&md5=738b79a0ccc292685f2cd712f8b7f0d0

DOI: 10.1007/s10719-016-9730-y

Nikishin, G.I., Kapustina, N.I., Sokova, L.L., Bityukov, O.V., Terent'ev, A.O.
One-pot oxidative bromination – Esterification of aldehydes to 2-bromoesters using cerium (IV) ammonium nitrate and lithium bromide
(2017) Tetrahedron Letters, 58 (4), pp. 352-354. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85007487747&doi=10.1016%2fj.tetlet.2016.12.036&partnerID=40&md5=f60c719df0886272010133c10c912406

DOI: 10.1016/j.tetlet.2016.12.036

Hanske, J., Schulze, J., Aretz, J., McBride, R., Loll, B., Schmidt, H., Knirel, Y., Rabsch, W., Wahl, M.C., Paulson, J.C., Rademacher, C.
Bacterial polysaccharide specificity of the pattern recognition receptor langerin is highly species-dependent
(2017) Journal of Biological Chemistry, 292 (3), pp. 862-871. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010333012&doi=10.1074%2fjbc.M116.751750&partnerID=40&md5=bd79efe3f3b11b69281eed49574c7f0a

DOI: 10.1074/jbc.M116.751750

Lempert, D.B., Sheremetev, A.B.
The energetic potential of azo- and azoxyfurazan nitro derivatives as components of composite rocket propellants
(2017) Chemistry of Heterocyclic Compounds, pp. 1-8. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009858744&doi=10.1007%2fs10593-017-2008-x&partnerID=40&md5=f734df86102dcd1876552927d898c5ab

DOI: 10.1007/s10593-017-2008-x

Verkhnyatskaya, S.A., Krylov, V.B., Nifantiev, N.E.
Pyranoside-into-Furanoside Rearrangement of 4-Pentenyl Glycosides in the Synthesis of a Tetrasaccharide-Related to Galactan I of Klebsiella pneumoniae
(2017) European Journal of Organic Chemistry, 2017 (3), pp. 710-718. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010665871&doi=10.1002%2fejoc.201601413&partnerID=40&md5=977484f7c323f0d63f219b3e46fb529a

DOI: 10.1002/ejoc.201601413

Dalinger, I.L., Kormanov, A.V., Vatsadze, I.A., Serushkina, O.V., Shkineva, T.K., Suponitsky, K.Y., Pivkina, A.N., Sheremetev, A.B.
Synthesis of 1- and 5-(pyrazolyl)tetrazole amino and nitro derivatives
(2017) Chemistry of Heterocyclic Compounds, pp. 1-10. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009742503&doi=10.1007%2fs10593-017-2003-2&partnerID=40&md5=7912bc8208c9b46a373937631e941c07

DOI: 10.1007/s10593-017-2003-2

Eurtivong, C., Semenov, V., Semenova, M., Konyushkin, L., Atamanenko, O., Reynisson, J., Kiselyov, A.
3-Amino-thieno[2,3-b]pyridines as microtubule-destabilising agents: Molecular modelling and biological evaluation in the sea urchin embryo and human cancer cells
(2017) Bioorganic and Medicinal Chemistry, 25 (2), pp. 658-664. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006857277&doi=10.1016%2fj.bmc.2016.11.041&partnerID=40&md5=3e260a0a134078bd78238f1e25730a65

DOI: 10.1016/j.bmc.2016.11.041

Panferova, L.I., Smirnov, V.O., Levin, V.V., Kokorekin, V.A., Struchkova, M.I., Dilman, A.D.
Synthesis of 3-Fluoroindoles via Photoredox Catalysis
(2017) Journal of Organic Chemistry, 82 (1), pp. 745-753. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018479835&doi=10.1021%2facs.joc.6b02344&partnerID=40&md5=0d0649c3e2ad1dd11158419a1b8b7b98

DOI: 10.1021/acs.joc.6b02344

Salikov, R.F., Trainov, K.P., Levina, A.A., Belousova, I.K., Medvedev, M.G., Tomilov, Y.V.
Synthesis of Branched Tryptamines via the Domino Cloke-Stevens/Grandberg Rearrangement
(2017) Journal of Organic Chemistry, 82 (1), pp. 790-795. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018476323&doi=10.1021%2facs.joc.6b02578&partnerID=40&md5=3d63ec4e18a30613b068d9f8e8462d0e

DOI: 10.1021/acs.joc.6b02578

Medvedev, M.G., Bushmarinov, I.S., Sun, J., Perdew, J.P., Lyssenko, K.A.
Density functional theory is straying from the path toward the exact functional
(2017) Science, 355 (6320), art. no. aah5975, . Cited 9 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009265616&doi=10.1126%2fscience.aah5975&partnerID=40&md5=2381f377171d86c4ff3e40a9671f0d52

DOI: 10.1126/science.aah5975

Semenov, V.V., Lichitsky, B.V., Komogortsev, A.N., Dudinov, A.A., Krayushkin, M.M., Konyushkin, L.D., Atamanenko, O.P., Karmanova, I.B., Strelenko, Y.A., Shor, B., Semenova, M.N., Kiselyov, A.S.
Synthesis and anti-mitotic activity of 6,7-dihydro-4H-isothiazolo[4,5-b]pyridin-5-ones: In vivo and cell-based studies
(2017) European Journal of Medicinal Chemistry, 125, pp. 573-585. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989947718&doi=10.1016%2fj.ejmech.2016.09.075&partnerID=40&md5=3d78922550c53c2c9b92779da281e754

DOI: 10.1016/j.ejmech.2016.09.075

Kononov, L.O., Fedina, K.G., Orlova, A.V., Kondakov, N.N., Abronina, P.I., Podvalnyy, N.M., Chizhov, A.O.
Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?
(2017) Carbohydrate Research, 437, pp. 28-35. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85004045190&doi=10.1016%2fj.carres.2016.11.009&partnerID=40&md5=4f91217d3859e6c3764a44fb797f0ba8

DOI: 10.1016/j.carres.2016.11.009

Pyatakov, D.A., Astakhov, A.V., Sokolov, A.N., Fakhrutdinov, A.N., Fitch, A.N., Rybakov, V.B., Chernyshev, V.V., Chernyshev, V.M.
Alkoxy base-mediated selective synthesis and new rearrangements of 1,2,4-triazolodipyrimidinones
(2017) Tetrahedron Letters, 58 (8), pp. 748-754. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009929124&doi=10.1016%2fj.tetlet.2017.01.030&partnerID=40&md5=f92d541ca98703aa0d18f48de9d3e597

DOI: 10.1016/j.tetlet.2017.01.030

Yashin, A.Y., Yashunsky, D.V., Vedenin, A.N., Nifantiev, N.E., Yashin, Y.I., Nemzer, B.V.
Antioxidant activity of polyphenols from larch wood: an amperometric study
(2017) Nutrition and Food Science, 47 (2), pp. 297-303. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016945790&doi=10.1108%2fNFS-05-2016-0064&partnerID=40&md5=ec7dae9cc389fdfc5a8320c324ae02b2

DOI: 10.1108/NFS-05-2016-0064

Kuznetsov, N.Yu., Tikhov, R.M., Godovikov, I.A., Medvedev, M.G., Lyssenko, K.A., Burtseva, E.I., Kirillova, E.S., Bubnov, Y.N.
Stereoselective synthesis of novel adamantane derivatives with high potency against rimantadine-resistant influenza A virus strains
(2017) Organic and Biomolecular Chemistry, 15 (15), pp. 3152-3157. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017497156&doi=10.1039%2fc7ob00331e&partnerID=40&md5=16daf345308dd77da28d92dc6294c5ff

DOI: 10.1039/c7ob00331e

Zelenov, V.P., Bukalov, S.S., Leites, L.A., Aysin, R.R., Subbotin, A.N., Struchkova, M.I., Fedyanin, I.V.
Trifluoroacetyl nitrate
(2017) Mendeleev Communications, 27 (1), pp. 31-34. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010378948&doi=10.1016%2fj.mencom.2017.01.009&partnerID=40&md5=158ac760321b5550d290b5091c63f7ef

DOI: 10.1016/j.mencom.2017.01.009

Chirkova, Z.V., Kabanova, M.V., Filimonov, S.I., Abramov, I.G., Samet, A.V., Stashina, G.A., Suponitsky, K.Y.
The C-3 acylation of 1-hydroxyindoles
(2017) Tetrahedron Letters, 58 (8), pp. 755-757. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009830190&doi=10.1016%2fj.tetlet.2017.01.025&partnerID=40&md5=331fe78dd66202e407ec5a7ee77f5a93

DOI: 10.1016/j.tetlet.2017.01.025

Vinnitskiy, D.Z., Ustyuzhanina, N.E., Dmitrenok, A.S., Shashkov, A.S., Nifantiev, N.E.
Synthesis and NMR analysis of model compounds related to fucosylated chondroitin sulfates: GalNAc and Fuc(1 → 6)GalNAc derivatives
(2017) Carbohydrate Research, 438, pp. 9-17. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85003016109&doi=10.1016%2fj.carres.2016.11.015&partnerID=40&md5=6edcde6dc154b2cd1aa21ea60778d9e3

DOI: 10.1016/j.carres.2016.11.015

Varbanets, L.D., Zdorovenko, E.A., Brovarskaya, O.S., Kalinichenko, S.V.
Characterization of the lipopolysaccharide of Escherichia coli 126
(2017) Microbiology (Russian Federation), 86 (1), pp. 56-63. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013037513&doi=10.1134%2fS0026261717010167&partnerID=40&md5=021017f40bd1da3bef83fd6a2845b6fe

DOI: 10.1134/S0026261717010167

Han, R., Perepelov, A.V., Wang, Y., Filatov, A.V., Wang, M., Shashkov, A.S., Wang, L., Knirel, Y.A.
Structural and genetic characterization of the O-antigen of Enterobacter cloacae C5529 related to the O-antigen of E. cloacae G3054
(2017) Carbohydrate Research, 443-444, pp. 49-52. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015930140&doi=10.1016%2fj.carres.2017.02.006&partnerID=40&md5=7b3914b075e960f69e1a281a6c3fdd08

DOI: 10.1016/j.carres.2017.02.006

Tkachenko, O.P., Kucherov, A.V., Kustov, L.M., Virkkunen, V., Leinonen, T., Denifl, P.
A study of Ziegler-Natta propylene polymerization catalysts by spectroscopic methods
(2017) Materials, 10 (5), art. no. 496, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018868386&doi=10.3390%2fma10050496&partnerID=40&md5=a3066a09d1aa6a363b33c3396d3ddc56

DOI: 10.3390/ma10050496

Vil, V.A., Yaremenko, I.A., Ilovaisky, A.I., Terent'ev, A.O.
Synthetic strategies for peroxide ring construction in artemisinin
(2017) Molecules, 22 (1), art. no. 136, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009470021&doi=10.3390%2fmolecules22010117&partnerID=40&md5=e12f6ed84ca2985e6b77098528eba8c5

DOI: 10.3390/molecules22010117

Belen'kii, L.I., Evdokimenkova, Y.B.
The Literature of Heterocyclic Chemistry, Part XIV, 2014
(2017) Advances in Heterocyclic Chemistry, 122, pp. 245-301. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006972525&doi=10.1016%2fbs.aihch.2016.09.002&partnerID=40&md5=069d82188d94ecf36f463f95ba9e1a9f

DOI: 10.1016/bs.aihch.2016.09.002

Zanyatkin, I., Stroylova, Y., Tishina, S., Stroylov, V., Melnikova, A., Haertle, T., Muronetz, V.
Inhibition of Prion Propagation by 3,4-Dimethoxycinnamic Acid
(2017) Phytotherapy Research, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019424297&doi=10.1002%2fptr.5824&partnerID=40&md5=dc8bac0970b352c9fe314ac4fe060fa3

DOI: 10.1002/ptr.5824

Egorova, K.S., Toukach, P.V.
CSDB-GT: A new curated database on glycosyltransferases
(2017) Glycobiology, 27 (4), pp. 285-290. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019553099&doi=10.1093%2fglycob%2fcww137&partnerID=40&md5=864204de4e7c99b08443577fcdb92428

DOI: 10.1093/glycob/cww137

Yaremenko, I.A., Syroeshkin, M.A., Levitsky, D.O., Fleury, F., Terent’ev, A.O.
Cyclic peroxides as promising anticancer agents: in vitro cytotoxicity study of synthetic ozonides and tetraoxanes on human prostate cancer cell lines
(2017) Medicinal Chemistry Research, 26 (1), pp. 170-179. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994454876&doi=10.1007%2fs00044-016-1736-2&partnerID=40&md5=44c5d3b55ab38cb4b88c775ee44ca09b

DOI: 10.1007/s00044-016-1736-2

Shvetsova, S.V., Shabalin, K.A., Bobrov, K.S., Ivanen, D.R., Ustyuzhanina, N.E., Krylov, V.B., Nifantiev, N.E., Naryzhny, S.N., Zgoda, V.G., Eneyskaya, E.V., Kulminskaya, A.A.
Characterization of a new α-L-fucosidase isolated from Fusarium proliferatum LE1 that is regioselective to α-(1 → 4)-L-fucosidic linkage in the hydrolysis of α-L-fucobiosides
(2017) Biochimie, 132, pp. 54-65. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84995513642&doi=10.1016%2fj.biochi.2016.10.014&partnerID=40&md5=134c68d74e57a3b48dc996c4812090a9

DOI: 10.1016/j.biochi.2016.10.014

Muravyev, N.V., Monogarov, K.A., Asachenko, A.F., Nechaev, M.S., Ananyev, I.V., Fomenkov, I.V., Kiselev, V.G., Pivkina, A.N.
Pursuing reliable thermal analysis techniques for energetic materials: Decomposition kinetics and thermal stability of dihydroxylammonium 5,5′-bistetrazole-1,1′-diolate (TKX-50)
(2017) Physical Chemistry Chemical Physics, 19 (1), pp. 436-449. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016162922&doi=10.1039%2fc6cp06498a&partnerID=40&md5=55be6bf143d1be7f8e80cb98c70f0974

DOI: 10.1039/c6cp06498a

Pavlov, V.A., Pavlova, T.N.
Paradoxes of symmetry: Homochirality; cryptochiral reactions; chiral field, memory, and induction; chiral and racemic environment
(2017) Current Organic Chemistry, 21 (10), pp. 872-888. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018388615&doi=10.2174%2f1385272821666161128115134&partnerID=40&md5=acd163ec3ad4f5395497dce427f51c10

DOI: 10.2174/1385272821666161128115134

Gromovykh, T.I., Sadykova, V.S., Lutcenko, S.V., Dmitrenok, A.S., Feldman, N.B., Danilchuk, T.N., Kashirin, V.V.
Bacterial cellulose synthesized by Gluconacetobacter hansenii for medical applications
(2017) Applied Biochemistry and Microbiology, 53 (1), pp. 60-67. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013441138&doi=10.1134%2fS0003683817010094&partnerID=40&md5=7c8162700cc9a5f0980896e1d60ca026

DOI: 10.1134/S0003683817010094

Vedenyapina, M.D., Strel’tsova, E.D., Sharpai, Y.V., Terent’ev, A.O., Vedenyapin, A.A.
Adsorption of ethyl benzoate on activated carbon
(2017) Solid Fuel Chemistry, 51 (1), pp. 44-47. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013952656&doi=10.3103%2fS0361521917010116&partnerID=40&md5=bb2c8a8908a1dda74fcb80dbf64a374f

DOI: 10.3103/S0361521917010116

Rohdenburg, M., Mayer, M., Grellmann, M., Jenne, C., Borrmann, T., Kleemiss, F., Azov, V.A., Asmis, K.R., Grabowsky, S., Warneke, J.
Superelectrophilic Behavior of an Anion Demonstrated by the Spontaneous Binding of Noble Gases to [B<inf>12</inf>Cl<inf>11</inf>]-
(2017) Angewandte Chemie - International Edition, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019703512&doi=10.1002%2fanie.201702237&partnerID=40&md5=ff09c63e4fdc6f681946443eed32d543

DOI: 10.1002/anie.201702237

Aleksandrov, A.I., Akopova, T.A., Shevchenko, V.G., Cherkaev, G.V., Degtyarev, E.N., Dubinskii, A.A., Krasovskii, V.G., Prokof’ev, A.I., Abramchuk, S.S., Buzin, M.I.
A biocompatible nanocomposite based on allyl chitosan and vinyltriethoxysilane for tissue engineering
(2017) Polymer Science - Series B, 59 (1), pp. 97-108. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85014954440&doi=10.1134%2fS1560090417010018&partnerID=40&md5=e1d805fc055190c4eda7a3fe2dbb08af

DOI: 10.1134/S1560090417010018

Vinogradov, M.G., Turova, O.V., Zlotin, S.G.
The progress in the chemistry of N-Acyliminium ions &amp; their use in stereoselective organic synthesis
(2017) Russian Chemical Reviews, 86 (1), pp. 1-17. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85011552195&doi=10.1070%2fRCR4628&partnerID=40&md5=be0f2128d260ca6187f6328893903eef

DOI: 10.1070/RCR4628

Serenko, O., Strashnov, P., Kapustin, G., Kalinin, M., Kuchkina, N., Serkova, E., Shifrina, Z., Muzafarov, A.
Adsorption properties of pyridylphenylene dendrimers
(2017) RSC Advances, 7 (13), pp. 7870-7875. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010653622&doi=10.1039%2fc6ra27064f&partnerID=40&md5=ba10065a638b2017cbe2b16a969230e3

DOI: 10.1039/c6ra27064f

Greish, A.A., Glukhov, L.M., Kustov, L.M.
Oxidative dehydrogenation of dimethyl ether to 1,2-dimethoxyethane over oxide catalysts
(2017) Mendeleev Communications, 27 (1), pp. 72-74. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010457888&doi=10.1016%2fj.mencom.2017.01.023&partnerID=40&md5=f67930229af2866823451d2168a55985

DOI: 10.1016/j.mencom.2017.01.023

Shestakov, A.S., Moustafa, A.H., Bushmarinov, I.S., Goloveshkin, A.S., Shapovalov, A.V., Shikhaliev, K.S., Prezent, M.A., Sidorenko, O.E.
Detailed Studies of the Alkylation Sides of Pyridin-2-yl and 4,6-Dimethylpyrimidin-2-yl-cyanamides
(2017) Journal of Heterocyclic Chemistry, 54 (1), pp. 551-560. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961751206&doi=10.1002%2fjhet.2621&partnerID=40&md5=1a0449ef115a705e4e2417c6a84bf017

DOI: 10.1002/jhet.2621

Ivanov, S.M., Shestopalov, A.M., Mironovich, L.M., Rodinovskaya, L.A.
One-pot Method for Reduction of Pyrazolo[5,1-c][1,2,4]Triazine-7-diazonium Tetrafluoroborate to 7-Hydrazinyl Derivatives
(2017) Journal of Heterocyclic Chemistry, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017640108&doi=10.1002%2fjhet.2874&partnerID=40&md5=922c6d851445ba8fbe4ea9e01ba54e43

DOI: 10.1002/jhet.2874

Badikova, A.D., Kulyashova, I.N., Kudasheva, F.K., Tsadkin, M.A., Mortikov, E.S., Yalalova, R.A.
Modification of Neutral Sulfite Liquors with Production of Lignosulfonate Drilling Reagents
(2017) Chemistry and Technology of Fuels and Oils, 52 (6), pp. 656-662. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85014648170&doi=10.1007%2fs10553-017-0757-y&partnerID=40&md5=d6d70f9d5c6c4de3580523ebf1515342

DOI: 10.1007/s10553-017-0757-y

 

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В интервью газете "Поиск" сотрудник ИОХ РАН член-корреспондент РАН Валентин Анаников рассказывает о новом проекте по биопластикам и о том, как изменилась работа российских ученых после появления в стране Российского научного фонда (РНФ).
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