РУС ENG
Министерство науки и высшего образования Российской Федерации
Российская Академия Наук

Публикации за 2016 год

Rassokhina, I.V., Volkova, Y.A., Kozlov, A.S., Scherbakov, A.M., Andreeva, O.E., Shirinian, V.Z., Zavarzin, I.V.
Synthesis and antiproliferative activity evaluation of steroidal imidazo[1,2-A]pyridines
(2016) Steroids, 113, pp. 29-37. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84975263373&partnerID=40&md5=703624a71195709dfbddf82833de3604

DOI: 10.1016/j.steroids.2016.06.001

Minyaev, M.E., Vinogradov, A.A., Roitershtein, D.M., Borisov, R.S., Ananyev, I.V., Churakov, A.V., Nifant'Ev, I.E.
Catalytic activity of phenyl substituted cyclopentadienyl neodymium complexes in the ethylene oligomerization process
(2016) Journal of Organometallic Chemistry, 818, pp. 128-136. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84973861964&partnerID=40&md5=a7b2b44e3b6badec15c3e7e5ad8843dd

DOI: 10.1016/j.jorganchem.2016.06.003

Isaev, A.N.
Intermolecular charge transfer as evidence for unusual O-H...C(sp3) hydrogen bond
(2016) Computational and Theoretical Chemistry, 1090, pp. 180-192. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84975727034&partnerID=40&md5=9bd98aef55c79fb2d5ac14d6a8902d83

DOI: 10.1016/j.comptc.2016.06.014

Podvalnyy, N.M., Chizhov, A.O., Zinin, A.I., Kononov, L.O.
Rapid synthesis of linear homologous oligoarabinofuranosides related to mycobacterial lipoarabinomannan and a neoglycoconjugate thereof
(2016) Carbohydrate Research, 431, pp. 25-32. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84971641012&partnerID=40&md5=481a548e7bc7c330bf0698ed60159139

DOI: 10.1016/j.carres.2016.05.009

Nikulshin, P.A., Salnikov, V.A., Varakin, A.N., Kogan, V.M.
The use of CoMoS catalysts supported on carbon-coated alumina for hydrodeoxygenation of guaiacol and oleic acid
(2016) Catalysis Today, 271, pp. 45-55. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84938795198&partnerID=40&md5=a800af643998669be87dd7dd97e45f1f

DOI: 10.1016/j.cattod.2015.07.032

Kirichenko, O.A., Kapustin, G.I., Tkachenko, O.P., Nissenbaum, V.D., Mishin, I.V., Davshan, N.A., Redina, E.A., Kustov, L.M.
Synthesis and characterization of novel Au/θ-Al<inf>2-x</inf>Fe<inf>x</inf>O<inf>3</inf> nanomaterials with high thermal stability in catalytic oxidation of carbon monoxide
(2016) Materials Research Bulletin, 80, pp. 139-149. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962815486&partnerID=40&md5=e78bd282baf1d8ce9e186571483d5346

DOI: 10.1016/j.materresbull.2016.03.042

Chen, C., Liu, B., Xu, Y., Utkina, N., Zhou, D., Danilov, L., Torgov, V., Veselovsky, V., Feng, L.
Biochemical characterization of the novel α-1, 3-galactosyltransferase WclR from Escherichia coli O3
(2016) Carbohydrate Research, 430, pp. 36-43. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84968783399&partnerID=40&md5=501c564028033b05457b9768d57cfc13

DOI: 10.1016/j.carres.2016.04.012

Shashkov, A.S., Zhang, Y., Sun, Q., Guo, X., Senchenkova, S.N., Perepelov, A.V., Knirel, Y.A.
Structure and gene cluster of the O-antigen of Escherichia coli O133
(2016) Carbohydrate Research, 430, pp. 82-84. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969940857&partnerID=40&md5=90033dfebc4cd80311aba2ec14017b2a

DOI: 10.1016/j.carres.2016.04.028

Duan, Z., Senchenkova, S.N., Guo, X., Perepelov, A.V., Shashkov, A.S., Liu, B., Knirel, Y.A.
Structure and gene cluster of the O-antigen of Escherichia coli O156 containing a pyruvic acid acetal
(2016) Carbohydrate Research, 430, pp. 24-28. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84966309367&partnerID=40&md5=a5f80c6e5ce16b1e4896c38b15155589

DOI: 10.1016/j.carres.2016.04.025

Chilingarov, N.S., Medvedev, A.A., Deyko, G.S., Kustov, L.M., Chernikova, E.A., Glukhov, L.M., Polyakova, M.V., Ioutsi, V.A., Markov, V.Y., Sidorov, L.N.
The evaporation study of silicon-containing ionic liquid
(2016) Chemical Physics Letters, 657, pp. 8-10. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84970977771&partnerID=40&md5=fdbe91643f95ebd4a3badf9f8a27040c

DOI: 10.1016/j.cplett.2016.05.015

Stakheev, A.Y., Mashkovsky, I.S., Bragina, G.O., Baeva, G.N., Telegina, N.S., Malmstrøm Larsen, K., Kustov, A.L., Thøgersen, J.R.
Mechanism of Low-Temperature NO<inf>x</inf> Storage for Reducing NO<inf>x</inf> Cold Start Emission
(2016) Topics in Catalysis, 59 (10-12), pp. 931-937. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84977136787&partnerID=40&md5=8eff924f90f2ec1959f54192a833e49d

DOI: 10.1007/s11244-016-0571-5

Krylov, V.B., Argunov, D.A., Vinnitskiy, D.Z., Gerbst, A.G., Ustyuzhanina, N.E., Dmitrenok, A.S., Nifantiev, N.E.
The Pyranoside- into -Furanoside Rearrangement of Alkyl Glycosides: Scope and Limitations
(2016) Synlett, 27 (11), art. no. st-2016-d0011-l, pp. 1659-1664. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964054441&partnerID=40&md5=e672166fe8653477ea21865f8f038adc

DOI: 10.1055/s-0035-1561595

Shashkov, A.S., Streshinskaya, G.M., Tul’skaya, E.M., Senchenkova, S.N., Baryshnikova, L.M., Dmitrenok, A.S., Ostash, B.E., Fedorenko, V.A.
Cell wall glycopolymers of Streptomyces albus, Streptomyces albidoflavus and Streptomyces pathocidini
(2016) Antonie van Leeuwenhoek, International Journal of General and Molecular Microbiology, 109 (7), pp. 923-936. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964027496&partnerID=40&md5=104dc037cff01db18db7c5e36ceb87f0

DOI: 10.1007/s10482-016-0691-8

Mytareva, A.I., Stakheev, A.Y., Baeva, G.N., Bokarev, D.A., Kustov, A.L., Thøgersen, J.R.
New Insights into the Mechanism of Synergistic Effect for [CeO<inf>2</inf>–ZrO<inf>2</inf> + H-Beta] CombiCat in NH<inf>3</inf>–SCR
(2016) Topics in Catalysis, 59 (10-12), pp. 919-924. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84977178233&partnerID=40&md5=7115060e357ee62a11a15217ebc68aa1

DOI: 10.1007/s11244-016-0569-z

Knirel, Y.A., Qian, C., Senchenkova, S.N., Guo, X., Shashkov, A.S., Chizhov, A.O., Perepelov, A.V., Liu, B.
Structure of the β-l-fucopyranosyl phosphate-containing O-specific polysaccharide of Escherichia coli O84
(2016) International Journal of Biological Macromolecules, 88, pp. 578-585. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964316649&partnerID=40&md5=89e557f1c1ad4a79b93046a1ee3eb4b6

DOI: 10.1016/j.ijbiomac.2016.04.025

Barsukov, D.V., Pershin, A.N., Subbotina, I.R.
Increase of CO photocatalytic oxidation rate over anatase TiO<inf>2</inf> particles by adsorbed water at moderate coverages: The role of peroxide species
(2016) Journal of Photochemistry and Photobiology A: Chemistry, 324, pp. 175-183. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962833134&partnerID=40&md5=fc8b64f80579e300ddcc312422778004

DOI: 10.1016/j.jphotochem.2016.03.021

Kulikova, N.A., Abroskin, D.P., Badun, G.A., Chernysheva, M.G., Korobkov, V.I., Beer, A.S., Tsvetkova, E.A., Senik, S.V., Klein, O.I., Perminova, I.V.
Label Distribution in Tissues of Wheat Seedlings Cultivated with Tritium-Labeled Leonardite Humic Acid
(2016) Scientific Reports, 6, art. no. 28869, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84976544774&partnerID=40&md5=f7bac5060571f35b4740cf11ddaacdd4

DOI: 10.1038/srep28869

Kapaev, R.R., Toukach, P.V.
Simulation of 2D NMR Spectra of Carbohydrates Using GODESS Software
(2016) Journal of Chemical Information and Modeling, 56 (6), pp. 1100-1104. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84976447859&partnerID=40&md5=94a156ce0eff8fae3f9fa4c652fc7d5b

DOI: 10.1021/acs.jcim.6b00083

Semyakin, S.S., Struchkova, M.I., Sheremetev, A.B.
A Novel Mild Method for the Synthesis of 3-Amino-4-(5-aryl-1H-1,2,4-Triazol-3-yl)Furazans
(2016) Chemistry of Heterocyclic Compounds, pp. 1-4. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84976273931&partnerID=40&md5=ea98e133d97cf4a15cb0bb8cb891b63b

DOI: 10.1007/s10593-016-1888-5
DOCUMENT TYPE: Article in Press

Kochkin, D.V., Khandy, M.T., Zaitsev, G.P., Tolkacheva, N.V., Shashkov, A.S., Titova, M.V., Chirva, V.Y., Nosov, A.M.
Protodioscin in Dioscorea deltoidea Suspension Cell Culture
(2016) Chemistry of Natural Compounds, pp. 1-5. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84975488512&partnerID=40&md5=5faa01a21b39dad32e1f1d7eda6a3e42

DOI: 10.1007/s10600-016-1734-0
DOCUMENT TYPE: Article in Press

Terent'Ev, A.O., Pastukhova, Z.Y., Yaremenko, I.A., Novikov, R.A., Demchuk, D.V., Bruk, L.G., Levitsky, D.O., Fleury, F., Nikishin, G.I.
Selective transformation of tricyclic peroxides with pronounced antischistosomal activity into 2-hydroxy-1,5-diketones using iron (II) salts
(2016) Tetrahedron, 72 (24), pp. 3421-3426. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84965175034&partnerID=40&md5=7ba1c571409625dce96f20a390ce9baa

DOI: 10.1016/j.tet.2016.04.054

Arzumanyan, A.V., Terent'Ev, A.O., Novikov, R.A., Lakhtin, V.G., Grigoriev, M.S., Nikishin, G.I.
Reduction of Organosilicon Peroxides: Ring Contraction and Cyclodimerization
(2016) Organometallics, 35 (11), pp. 1667-1673. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84974782512&partnerID=40&md5=7b50e01d9b08fd41aedfe54279e8db69

DOI: 10.1021/acs.organomet.6b00129

Panova, Y.S., Kashin, A.S., Vorobev, M.G., Degtyareva, E.S., Ananikov, V.P.
Nature of the copper-oxide-mediated C-S cross-coupling reaction: Leaching of catalytically active species from the metal oxide surface
(2016) ACS Catalysis, 6 (6), pp. 3637-3643. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84973647690&partnerID=40&md5=fa7bb88e1a5e313e642cb9797533988c

DOI: 10.1021/acscatal.6b00337

Shashkov, A.S., Zhang, W., Perepelov, A.V., Weintraub, A., Liu, B., Widmalm, G., Knirel, Y.A.
Structure of the O-polysaccharide of Escherichia coli O132
(2016) Carbohydrate Research, 427, pp. 44-47. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84963538102&partnerID=40&md5=7580a782725dd16744410d0cac25b7ef

DOI: 10.1016/j.carres.2016.03.016

Perepelov, A.V., Filatov, A.V., Wang, M., Shashkov, A.S., Wang, L., Knirel, Y.A.
Structure and gene cluster of the O-antigen of Enterobacter cloacae G3421
(2016) Carbohydrate Research, 427, pp. 55-59. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964794094&partnerID=40&md5=f35076f9847eba2293f82863639544c8

DOI: 10.1016/j.carres.2016.03.008

Novikov, R.A., Tarasova, A.V., Tomilov, Y.V.
GaCl<inf>3</inf>-Mediated Isomerization of Donor-Acceptor Cyclopropanes into (2-Arylalkylidene)malonates
(2016) Synlett, 27 (9), art. no. st-2015-b0897-l, pp. 1367-1370. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960145489&partnerID=40&md5=5250dd3623cc2a6e6658cd33ab58ce5f

DOI: 10.1055/s-0035-1561389

Knirel, Y.A., Qian, C., Shashkov, A.S., Sizova, O.V., Zdorovenko, E.L., Naumenko, O.I., Senchenkova, S.N., Perepelov, A.V., Liu, B.
Structural relationships between genetically closely related O-antigens of Escherichia coli and Shigella spp.
(2016) Biochemistry (Moscow), 81 (6), pp. 600-608. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84975678743&partnerID=40&md5=e750af447f8764a01cd308dee3a33353

DOI: 10.1134/S0006297916060067

Kustov, L.M., Furman, D.B., Barkova, A.P.
Metathesis of C<inf>5</inf>–C<inf>8</inf> Terminal Olefins on Re<inf>2</inf>O<inf>7</inf>/Al<inf>2</inf>O<inf>3</inf> Catalysts
(2016) Catalysis Letters, 146 (6), pp. 1033-1039. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961859316&partnerID=40&md5=05589a146c45dccc9f702f5c7dadd3a1

DOI: 10.1007/s10562-016-1698-5

Ivanov, E.V., Batov, D.V., Kravchenko, A.N.
(D<inf>2</inf>O-H<inf>2</inf>O) solvent isotope effects on some thermodynamic properties of the Albicar dissolution (hydration) between T = (278.15 and 313.15) K at ambient pressure
(2016) Journal of Chemical Thermodynamics, 97, pp. 341-347. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959376446&partnerID=40&md5=525bad23340386a4e41ca3cd44ab7221

DOI: 10.1016/j.jct.2016.02.012

Geisman, A.N., Valuev-Elliston, V.T., Ozerov, A.A., Khandazhinskaya, A.L., Chizhov, A.O., Kochetkov, S.N., Pannecouque, C., Naesens, L., Seley-Radtke, K.L., Novikov, M.S.
1,6-Bis[(benzyloxy)methyl]uracil derivatives — Novel antivirals with activity against HIV-1 and influenza H1N1 virus
(2016) Bioorganic and Medicinal Chemistry, 24 (11), pp. 2476-2485. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84963948615&partnerID=40&md5=4bbf0eac7058a35f4335a3d650fc8668

DOI: 10.1016/j.bmc.2016.04.010

Mishanin, I.I., Kalenchuk, A.N., Maslakov, K.I., Lunin, V.V., Koklin, A.E., Finashina, E.D., Bogdan, V.I.
Deactivation of a mixed oxide catalyst of Mo–V–Te–Nb–O composition in the reaction of oxidative ethane dehydrogenation
(2016) Russian Journal of Physical Chemistry A, 90 (6), pp. 1132-1136. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84971671373&partnerID=40&md5=c5c1ec7239445834fd1a78aff97d4334

DOI: 10.1134/S0036024416060133

Semenov, V.V., Tsyganov, D.V., Semenova, M.N., Chuprov-Netochin, R.N., Raihstat, M.M., Konyushkin, L.D., Volynchuk, P.B., Marusich, E.I., Nazarenko, V.V., Leonov, S.V., Kiselyov, A.S.
Efficient Synthesis of Glaziovianin A Isoflavone Series from Dill and Parsley Extracts and Their in Vitro/in Vivo Antimitotic Activity
(2016) Journal of Natural Products, 79 (5), pp. 1429-1438. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84971426137&partnerID=40&md5=c5353c5b91d5e7f512e675ac40ade680

DOI: 10.1021/acs.jnatprod.6b00173

Volkova, Y.A., Gorbatov, S.A.
1-Sulfonyl-1,2,3-triazoles as promising reagents in the synthesis of nitrogen-containing linear and heterocyclic structures (microreview)
(2016) Chemistry of Heterocyclic Compounds, pp. 1-3. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969920946&partnerID=40&md5=68007a365cb7eefd8e5d706362601d4b

DOI: 10.1007/s10593-016-1865-z
DOCUMENT TYPE: Article in Press

Gazieva, G.A., Anikina, L.V., Pukhov, S.A., Karpova, T.B., Nelyubina, Y.V., Kravchenko, A.N.
Substituted N-aminothioglycolurils containing thiosemicarbazone moiety and their cytotoxic activity in vitro
(2016) Molecular Diversity, pp. 1-10. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969833453&partnerID=40&md5=269c84d40afdb5aa20e833a7fe0eb35d

DOI: 10.1007/s11030-016-9671-1
DOCUMENT TYPE: Article in Press

Kirichenko, O.A., Davshan, N.A., Redina, E.A., Kapustin, G.I., Mishin, I.V., Tkachenko, O.P., Kucherov, A.V., Kustov, L.M.
Gold nanoparticles in environmental catalysis: Influence of the Fe-modified alumina supports on the catalytic behavior of supported gold nanoparticles in CO oxidation in the presence of ammonia
(2016) Chemical Engineering Journal, 292, pp. 62-71. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958528257&partnerID=40&md5=f435f2aec15a9784218692c64ec1f409

DOI: 10.1016/j.cej.2016.01.101

Shashkov, A.S., Yang, B., Senchenkova, S.N., Perepelov, A.V., Liu, B., Knirel, Y.A.
Structures and genetics of biosynthesis of glycerol 1-phosphate-containing O-polysaccharides of Escherichia coli O28ab, O37, and O100
(2016) Carbohydrate Research, 426, pp. 26-32. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962440512&partnerID=40&md5=14179d3f38d0e3ee5c4079176da8d834

DOI: 10.1016/j.carres.2016.03.011

Muravyev, N.V., Monogarov, K.A., Bragin, A.A., Fomenkov, I.V., Pivkina, A.N.
HP-DSC study of energetic materials. Part I. Overview of pressure influence on thermal behavior
(2016) Thermochimica Acta, 631, pp. 1-7. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962509194&partnerID=40&md5=5ae4e8856081480da7f1ab2348ff7b5e

DOI: 10.1016/j.tca.2016.03.018

Starosotnikov, A.M., Nikol'skiy, V.V., Borodulya, A.N., Kachala, V.V., Bastrakov, M.A., Solkan, V.N., Shevelev, S.A.
Synthesis and Functionalization of 5,7-Dinitroquinoline and Its N-Oxide
(2016) Asian Journal of Organic Chemistry, 5 (5), pp. 685-690. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961689605&partnerID=40&md5=292c26563fd03f6b4ac005fe93d1b2bb

DOI: 10.1002/ajoc.201600065

Kuptsov, A.H., Yashunsky, D.V., Ghosh, R., Albrecht, V., Bezdetnaya, L., Nifantiev, N.E.
Near IR spectroscopy of the solutions of a bacteriochlorin derivative as a quantitative method for the quality assurance of liquid products
(2016) Mendeleev Communications, 26 (3), pp. 261-263. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969915602&partnerID=40&md5=9d623212ac16f551242d20ed2e1ec512

DOI: 10.1016/j.mencom.2016.05.014

Terent'Ev, A.O., Sharipov, M.Y., Glinuskin, A.P., Krylov, I.B., Gaidarenko, D.V., Nikishin, G.I.
Difference in α-thiocyanation of malonates, β-oxo esters and β-diketones with sodium thiocyanate and cerium(IV) ammonium nitrate
(2016) Mendeleev Communications, 26 (3), pp. 226-227. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84970021250&partnerID=40&md5=1bd3770e00f6935959f2dd1e5213a6b3

DOI: 10.1016/j.mencom.2016.05.001

Finashina, E.D., Kramareva, N.V., Kucherov, A.V., Tkachenko, O.P., Kustov, L.M.
Preparation, characterization, and catalytic testing of different Me–chitosan complexes for triglycerides transesterification
(2016) Research on Chemical Intermediates, 42 (5), pp. 4907-4920. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84974827246&partnerID=40&md5=47f10f86da5dab419f0edb4fcd276a7f

DOI: 10.1007/s11164-015-2330-9

Vatsadze, S.Z., Shulga, D.A., Loginova, Y.D., Vatsadze, I.A., Wang, L., Yu, H., Kudryavtsev, K.V.
Computer modeling of ferrocene-substituted 3,7-diazabicyclo[3.3.1]nonanes as serine protease inhibitors
(2016) Mendeleev Communications, 26 (3), pp. 212-213. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84970016284&partnerID=40&md5=05a10bf4c2b4f7cda583b2b2e8824646

DOI: 10.1016/j.mencom.2016.04.011

Baykov, S.V., Zharov, A.A., Stashina, G.A., Zavarzin, I.V., Kofanov, E.R.
Reaction of amidoximes with acetonitrile at high pressure
(2016) Mendeleev Communications, 26 (3), pp. 264-265. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969988508&partnerID=40&md5=3b5970a980bb18803bce39660b97a6a9

DOI: 10.1016/j.mencom.2016.05.015

Drzewiecka, D., Shashkov, A.S., Arbatsky, N.P., Knirel, Y.A.
Immunochemical characterization of the O antigens of two Proteus strains, O8-related antigen of Proteus mirabilis 12 B-r and O2-related antigen of Proteus genomospecies 5/6 12 B-k, infecting a hospitalized patient in Poland
(2016) Microbiology (United Kingdom), 162 (5), art. no. 000274, pp. 789-797. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964940223&partnerID=40&md5=9f1380dc40275baa37b6071d24bb6856

DOI: 10.1099/mic.0.000274

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Shashkov, A.S., Kusaykin, M.I., Stonik, V.A., Nifantiev, N.E., Usov, A.I.
Structure and biological activity of a fucosylated chondroitin sulfate from the sea cucumber Cucumaria japonica
(2016) Glycobiology, 26 (5), pp. 449-459. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84965144158&partnerID=40&md5=2582296464899316d8c4f6a7811d73bf

DOI: 10.1093/glycob/cwv119

Kucherov, A.V.
Water as a key factor providing an easy migration/redistribution of Cu2+ species in CuO/HZSM-5
(2016) Mendeleev Communications, 26 (3), pp. 254-255. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969962262&partnerID=40&md5=e427a4832aff76073789047ccc1b3cb6

DOI: 10.1016/j.mencom.2016.05.011

Shashkov, A.S., Kenyon, J.J., Senchenkova, S.N., Shneider, M.M., Popova, A.V., Arbatsky, N.P., Miroshnikov, K.A., Volozhantsev, N.V., Hall, R.M., Knirel, Y.A.
Acinetobacter baumannii K27 and K44 capsular polysaccharides have the same K unit but different structures due to the presence of distinct wzy genes in otherwise closely related K gene clusters
(2016) Glycobiology, 26 (5), pp. 501-508. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84965124250&partnerID=40&md5=a06acc3e9ee6d466230ad71456cc03ab

DOI: 10.1093/glycob/cwv168

Starosotnikov, A.M., Bastrakov, M.A., Pavlov, A.A., Fedyanin, I.V., Dalinger, I.L., Shevelev, S.A.
Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan
(2016) Mendeleev Communications, 26 (3), pp. 217-219. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969931908&partnerID=40&md5=076c29c38210399786f614abed60196d

DOI: 10.1016/j.mencom.2016.04.013

Shesterkina, A.A., Kirichenko, O.A., Kozlova, L.M., Kapustin, G.I., Mishin, I.V., Strelkova, A.A., Kustov, L.M.
Liquid-phase hydrogenation of phenylacetylene to styrene on silica-supported Pd-Fe nanoparticles
(2016) Mendeleev Communications, 26 (3), pp. 228-230. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969916849&partnerID=40&md5=3c949392a99a94fdf118ec7f9aab2e98

DOI: 10.1016/j.mencom.2016.05.002

Konstantinova, L.S., Baranovsky, I.V., Irtegova, I.G., Bagryanskaya, I.Y., Shundrin, L.A., Zibarev, A.V., Rakitin, O.A.
Fused 1,2,3-dithiazoles: Convenient synthesis, structural characterization, and electrochemical properties
(2016) Molecules, 21 (5), art. no. 596, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84973661448&partnerID=40&md5=b84e67e8140b030740a6cca530e5ca02

DOI: 10.3390/molecules21050596

Naumovich, Y.A., Buckland, V.E., Sen'ko, D.A., Nelyubina, Y.V., Khoroshutina, Y.A., Sukhorukov, A.Yu., Ioffe, S.L.
Metal-assisted addition of a nitrate anion to bis(oxy)enamines. A general approach to the synthesis of α-nitroxy-oxime derivatives from nitronates
(2016) Organic and Biomolecular Chemistry, 14 (16), pp. 3963-3974. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969219503&partnerID=40&md5=216ce65b2bd000eea596462f78cf3475

DOI: 10.1039/c6ob00388e

Morozov, O.S., Gribanov, P.S., Asachenko, A.F., Dorovatovskii, P.V., Khrustalev, V.N., Rybakov, V.B., Nechaev, M.S.
Hydrohydrazination of Arylalkynes Catalyzed by an Expanded Ring N-Heterocyclic Carbene (er-NHC) Gold Complex under Solvent-Free Conditions
(2016) Advanced Synthesis and Catalysis, 358 (9), pp. 1463-1468. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959294984&partnerID=40&md5=c5910ec4a7660ee7cb8e076b4417e454

DOI: 10.1002/adsc.201500658

Tsyganov, D.V., Krayushkin, M.M., Konyushkin, L.D., Strelenko, Y.A., Semenova, M.N., Semenov, V.V.
Facile Synthesis of Natural Alkoxynaphthalene Analogues from Plant Alkoxybenzenes
(2016) Journal of Natural Products, 79 (4), pp. 923-928. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84967317320&partnerID=40&md5=88e0e95e7ea89f5c20277ef93c85831b

DOI: 10.1021/acs.jnatprod.5b01007

Maslov, M.Y., Plotnikova, T.M., Anishchenko, A.M., Aliev, O.I., Nifantiev, N.E., Plotnikov, M.B.
Hemorheological effects of secoisolariciresinol in ovariectomized rats
(2016) Biorheology, 53 (1), pp. 23-31. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84966600356&partnerID=40&md5=5e905ef84c422eaa7cf1ea1324ca8c4b

DOI: 10.3233/BIR-15066

Belov, N.A., Alentiev, A.Y., Ronova, I.A., Sinitsyna, O.V., Nikolaev, A.Y., Zharov, A.A.
Microstructure relaxation process of polyhexafluoropropylene after swelling in supercritical carbon dioxide
(2016) Journal of Applied Polymer Science, 133 (14), art. no. 43105, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84954372303&partnerID=40&md5=0c734f0fae73061d04506aa15b4a6cc8

DOI: 10.1002/app.43105

Zhou, D., Chen, C., Xu, L., Utkina, N., Danilov, L., Torgov, V., Veselovsky, V., Liu, B., Feng, L.
Mass spectrometric characterization of a two-glycosyltransferase tandem reaction for assembly of tetrasaccharide repeating unit of Escherichia coli O77 O-antigen
(2016) Carbohydrate Research, 424, pp. 24-29. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959537751&partnerID=40&md5=9e5c9987d569775247ad7855d867ae61

DOI: 10.1016/j.carres.2016.02.007

Sigida, E.N., Fedonenko, Y.P., Shashkov, A.S., Arbatsky, N.P., Zdorovenko, E.L., Konnova, S.A., Ignatov, V.V., Knirel, Y.A.
Elucidation of a masked repeating structure of the O-specific polysaccharide of the halotolerant soil bacteria Azospirillum halopraeferens Au4
(2016) Beilstein Journal of Organic Chemistry, 12, pp. 636-642. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84976321566&partnerID=40&md5=fd090f2173683661f89b8ccb95f36d3e

DOI: 10.3762/bjoc.12.62

Elinson, M.N., Ryzhkov, F.V., Zaimovskaya, T.A., Egorov, M.P.
Solvent-free multicomponent assembling of isatins, malononitrile, and dimedone: Fast and efficient way to functionalized spirooxindole system
(2016) Monatshefte fur Chemie, 147 (4), pp. 755-760. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960970217&partnerID=40&md5=9150b2ccb6f4ec6fcb5b127cb7557bb2

DOI: 10.1007/s00706-015-1617-2

Orekhov, A.S., Akunets, A.A., Borisenko, L.A., Gromov, A.I., Merkuliev, Y.A., Pimenov, V.G., Sheveleva, E.E., Vasiliev, V.G., Borisenko, N.G.
Modern trends in low-density materials for fusion
(2016) Journal of Physics: Conference Series, 688 (1), art. no. 012080, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964825676&partnerID=40&md5=4366b25f68d5624fe0199ebbd091423a

DOI: 10.1088/1742-6596/688/1/012080

Lempert, D.-B., Dalinger, I.-L., Shu, Y.-J., Kazakov, A.-I., Sheremetev, A.-B.
Estimation of the ballistic effectiveness of 3,4- and 3,5-dinitro-1-(trinitromethyl)-1H-pyrazoles as oxidizers for composite solid propellants
(2016) Huozhayao Xuebao/Chinese Journal of Explosives and Propellants, 39 (2), pp. 16-21. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84967163147&partnerID=40&md5=58f66320f11b5932ec9b72da86b1d1d9

DOI: 10.14077/j.issn.1007-7812.2016.02.003

Senchenkova, S.N., Zhang, Y., Perepelov, A.V., Guo, X., Shashkov, A.S., Weintraub, A., Liu, B., Widmalm, G., Knirel, Y.A.
Structure and gene cluster of the o-antigen of Escherichia coli O165 containing 5-N-acetyl- 7-N-[(R)-3-hydroxybutanoyl]pseudaminic acid
(2016) Glycobiology, 26 (4), pp. 335-342. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964871931&partnerID=40&md5=62f29f5afcd3048d0357c6e5c7af3fa3

DOI: 10.1093/glycob/cwv106

Senchenkova, S.N., Zhang, Y., Perepelov, A.V., Guo, X., Shashkov, A.S., Liu, B., Knirel, Y.A.
Structure and biosynthesis gene cluster of the O-antigen of Escherichia coli O12
(2016) Biochemistry (Moscow), 81 (4), pp. 401-406. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969813513&partnerID=40&md5=b51bd4a399356a3f1f7c5b06312e0a05

DOI: 10.1134/S0006297916040106

Aleksandrov, V.V., Bryzgunov, V.A., Grabovski, E.V., Gritsuk, A.N., Volobuev, I.V., Kazakov, E.D., Kalinin, Y.G., Korolev, V.D., Laukhin, Y.I., Medovshchikov, S.F., Mitrofanov, K.N., Oleinik, G.M., Pimenov, V.G., Smirnova, E.A., Ustroev, G.I., Frolov, I.N.
Measurements of the parameters of a condensed deuterated Z-pinch on the angara-5-1 facility
(2016) Plasma Physics Reports, 42 (4), pp. 355-361. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84970974308&partnerID=40&md5=34540153a4c2d0af6d8a095d22f3a7a0

DOI: 10.1134/S1063780X16040012

Zaitsev, K.V., Cherepakhin, V.S., Churakov, A.V., Peregudov, A.S., Tarasevich, B.N., Egorov, M.P., Zaitseva, G.S., Karlov, S.S.
Extending the family of stable heavier carbenes: New tetrylenes based on N,N,O-ligands
(2016) Inorganica Chimica Acta, 443, pp. 91-100. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84953455611&partnerID=40&md5=f94cff842afb1c2c5dc1d121e0d15dd2

DOI: 10.1016/j.ica.2015.12.025

Drenichev, M.S., Oslovsky, V.E., Sun, L., Tijsma, A., Kurochkin, N.N., Tararov, V.I., Chizhov, A.O., Neyts, J., Pannecouque, C., Leyssen, P., Mikhailov, S.N.
Modification of the length and structure of the linker of N6-benzyladenosine modulates its selective antiviral activity against enterovirus 71
(2016) European Journal of Medicinal Chemistry, 111, pp. 84-94. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957546069&partnerID=40&md5=cfd8e32cf9822a924b2f41cb03a120f0

DOI: 10.1016/j.ejmech.2016.01.036

Ivanov, E.V., Batov, D.V., Baranov, V.V., Kravchenko, A.N.
Temperature-dependent thermochemical properties of the Mebicaret (2,4-dimethyl-6,8-diethylglycoluril) solutions in H<inf>2</inf>O and D<inf>2</inf>O at the ambient pressure
(2016) Thermochimica Acta, 627-629, pp. 48-54. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84963619511&partnerID=40&md5=1a3239ecbed556e58c965c17e6112aab

DOI: 10.1016/j.tca.2016.01.010

Panferova, L.I., Tsymbal, A.V., Levin, V.V., Struchkova, M.I., Dilman, A.D.
Reactions of gem-Difluorinated Phosphonium Salts Induced by Light
(2016) Organic Letters, 18 (5), pp. 996-999. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960157688&partnerID=40&md5=21cd276dbad321344d595aa4cbeac14d

DOI: 10.1021/acs.orglett.6b00117

Perepelov, A.V., Guo, X., Senchenkova, S.N., Li, Y., Shashkov, A.S., Liu, B., Knirel, Y.A.
Structure and gene cluster of the O-antigen of Escherichia coli O137
(2016) Carbohydrate Research, 422, pp. 13-16. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84956713720&partnerID=40&md5=1d411b53dfe5acaa5cc9340a8e9bb98f

DOI: 10.1016/j.carres.2016.01.002

Rybakov, A.A., Bryukhanov, I.A., Larin, A.V., Zhidomirov, G.M.
Theoretical aspects of methanol carbonylation on copper-containing zeolites
(2016) Petroleum Chemistry, 56 (3), pp. 259-266. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84971268476&partnerID=40&md5=62f04755a782d2327bbd01944bd20d86

DOI: 10.1134/S0965544116030129

Pimenov, V.G., Sheveleva, E.E., Sakharov, A.M.
Use of freezing techniques for increasing the output of ultralow density laser targets
(2016) Instruments and Experimental Techniques, 59 (2), pp. 321-324. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969765316&partnerID=40&md5=98c180d5e443e1193db9a334c467c6a1

DOI: 10.1134/S0020441216010309

Grinevich, T.V., Solov’yanov, A.A., Vinogradov, D.B., Bulatov, P.V., Berlin, A.A.
Preparation of polyfunctional oligoethers
(2016) Doklady Chemistry, 467 (1), pp. 73-75. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84970956383&partnerID=40&md5=b5f2cecd23ee666ead37f203ab195b2d

DOI: 10.1134/S0012500816030058

Kravchenko, A.N., Chikunov, I.E., Gazieva, G.A., Makhova, N.N.
Efficient synthesis of N,N'-methylenebisglycolurils
(2016) Mendeleev Communications, 26 (2), pp. 136-138. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962157131&partnerID=40&md5=5c50979c27241b24f141dd24add606cf

DOI: 10.1016/j.mencom.2016.03.018

Mytareva, A.I., Bokarev, D.A., Baeva, G.N., Krivoruchenko, D.S., Belyankin, A.Y., Stakheev, A.Y.
Composite catalysts for selective catalytic reduction of NO<inf>x</inf> and oxidation of residual NH<inf>3</inf>
(2016) Petroleum Chemistry, 56 (3), pp. 211-216. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84971283612&partnerID=40&md5=600d0b5980042212309a4333484f7672

DOI: 10.1134/S0965544116030087

Nuriev, V.N., Vatsadze, I.A., Sviridenkova, N.V., Vatsadze, S.Z.
Synthesis of 3,7-disubstituted hexahydro- and tetrahydro-2H-indazoles from cross-conjugated dienones
(2016) Russian Journal of Organic Chemistry, 52 (3), pp. 389-396. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84970965923&partnerID=40&md5=edb3c52457d5953062d0c63341052df5

DOI: 10.1134/S1070428016030167

Khakimov, D.V., Pivina, T.S.
Calculated enthalpies of formation of 5,5'-bitetrazole salts
(2016) Mendeleev Communications, 26 (2), pp. 134-135. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962193465&partnerID=40&md5=2ade5c16569d321b563e2196a4873ca6

DOI: 10.1016/j.mencom.2016.03.017

Kuznetsov, V.V., Vedenyapina, M.D., Pleshchev, M.I., Gashev, S.B., Makhova, N.N., Vedenyapin, A.A.
Kinetics and mechanism of N-chloromethylamine decomposition in solutions
(2016) Russian Journal of Physical Chemistry A, 90 (3), pp. 541-544. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958794133&partnerID=40&md5=6b8565d100e70e14cab7adf64e024477

DOI: 10.1134/S0036024416030225

Gorshunova, K.K., Travkina, O.S., Kustov, L.M., Kutepov, B.I.
Synthesis and adsorption properties of the cation exchange forms of OFF-type zeolite
(2016) Russian Journal of Physical Chemistry A, 90 (3), pp. 652-657. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958818587&partnerID=40&md5=1e546022ab64a1e3fbc49baf0b54b9e3

DOI: 10.1134/S0036024416030122

Elinson, M.N., Dorofeeva, E.O., Vereshchagin, A.N., Korshunov, A.D., Egorov, M.P.
Simple and facile electrocatalytic approach to medicinally relevant spirocyclopropylpyrazolones directly from pyrazoline-5-ones and activated olefins
(2016) Research on Chemical Intermediates, 42 (3), pp. 2191-2200. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959932913&partnerID=40&md5=a6e7ab95107985926818cd0a6777cd79

DOI: 10.1007/s11164-015-2142-y

Isaev, A.N.
Hydrogen bonded C-H···Y (Y = O, S, Hal) molecular complexes: A natural bond orbital analysis
(2016) Russian Journal of Physical Chemistry A, 90 (3), pp. 601-609. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958756765&partnerID=40&md5=0c6d9d8823edf81fe1b1e901eef3d0f4

DOI: 10.1134/S0036024416030183

Matyugina, E.S., Valuev-Elliston, V.T., Chizhov, A.O., Kochetkov, S.N., Khandazhinskaya, A.L.
HIV-1 non-nucleoside reverse transcriptase inhibitors: Incorporation of benzylphosphonate moiety for solubility improvement
(2016) Mendeleev Communications, 26 (2), pp. 114-116. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962135607&partnerID=40&md5=34d8a440ab22fd7ff12be6b9774516c6

DOI: 10.1016/j.mencom.2016.03.009

Salazar, M., Hoffmann, S., Tkachenko, O.P., Becker, R., Grünert, W.
Hybrid catalysts for the selective catalytic reduction of NO by NH<inf>3</inf>: The influence of component separation on the performance of hybrid systems
(2016) Applied Catalysis B: Environmental, 182, pp. 213-219. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84942549009&partnerID=40&md5=f4c71dbf90090ed151be235c602d0abb

DOI: 10.1016/j.apcatb.2015.09.028

Keshtov, M.L., Kuklin, S.A., Godovskii, D.Y., Konstantinov, I.O., Krayushkin, M.M., Peregudov, A.S., Khokhlov, A.R.
Synthesis and optical and electrochemical properties of 5,6-bis[9-(2-decyltetradecyl)-9H-carbazol-3-yl]naphtho[2,1-b:3,4-b’]dithiophene as a promising building block for photovoltaic applications
(2016) Doklady Chemistry, 467 (1), pp. 94-99. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84971016488&partnerID=40&md5=74444d54bbb42748967232086e2fa6e1

DOI: 10.1134/S0012500816030022

Filatova, E.V., Turova, O.V., Kuchurov, I.V., Kostenko, A.A., Nigmatov, A.G., Zlotin, S.G.
Asymmetric catalytic synthesis of functionalized tetrahydroquinolines in supercritical fluids
(2016) Journal of Supercritical Fluids, 109, pp. 35-42. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84948410684&partnerID=40&md5=fdfce08f0a7da8ac211e46cf9f206acc

DOI: 10.1016/j.supflu.2015.11.004

Elinson, M.N., Vereshchagin, A.N., Bobrovsky, S.I., Nasybullin, R.F., Ilovaisky, A.I., Merkulova, V.M.
Pseudo four-component reaction of salicylaldehydes and cyclic ketones with two molecules of malononitrile: A facile and efficient way to synthesize 4-[2-(dicyanomethylene)cyclic or heterocyclic]-2-amino-4 H -chromenes
(2016) Comptes Rendus Chimie, 19 (3), pp. 292-297. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84951204799&partnerID=40&md5=61b27df4992a1764910fbf1fedcb43ad

DOI: 10.1016/j.crci.2015.11.002

Bakun, V.G., Saliev, A.N., Zemlyakov, N.D., Savost’yanov, A.P., Lapidus, A.L.
Structure and gasification of coal from the Gukovo-Gryaznovskoe deposit
(2016) Solid Fuel Chemistry, 50 (2), pp. 69-75. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969780162&partnerID=40&md5=ea50a9f031702fcf086755f56d7aeefb

DOI: 10.3103/S0361521916020026

Kryshtal, G.V., Zhdankina, G.M., Ignat'ev, N.V., Schulte, M., Zlotin, S.G.
The orthoester Johnson-Claisen rearrangement of allylic terpenols in the presence of acidic ionic liquid
(2016) Journal of Fluorine Chemistry, 183, pp. 23-29. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84956473122&partnerID=40&md5=b94b41585408241cf57562bb0c141473

DOI: 10.1016/j.jfluchem.2016.01.005

Zdvizhkov, A.T., Terent'Ev, A.O., Radulov, P.S., Novikov, R.A., Tafeenko, V.A., Chernyshev, V.V., Ilovaisky, A.I., Levitsky, D.O., Fleury, F., Nikishin, G.I.
Transformation of 2-allyl-1,3-diketones to bicyclic compounds containing 1,2-dioxolane and tetrahydrofuran rings using the I<inf>2</inf>/H<inf>2</inf>O<inf>2</inf> system
(2016) Tetrahedron Letters, 57 (8), pp. 949-952. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955457218&partnerID=40&md5=f3948b5280f4f42d6d54e7ae671e184e

DOI: 10.1016/j.tetlet.2016.01.061

Migulin, V.A.
Convenient and efficient synthesis of 2-methyl-5-nitrobenzo[b]thiophene and its derivatives
(2016) Synthetic Communications, pp. 1-6. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961208215&partnerID=40&md5=dc5344c008ce76ba5bfcef83c825506a

DOI: 10.1080/00397911.2015.1136645
DOCUMENT TYPE: Article in Press

Mendkovich, A.S., Syroeshkin, M.A., Nasybullina, D.V., Mikhailov, M.N., Gultyai, V.P., Elinson, M.N., Rusakov, A.I.
C-OH bond cleavage initiated by electron transfer: Electroreduction of 9-fluorenol
(2016) Electrochimica Acta, 191, pp. 962-973. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961309959&partnerID=40&md5=a6305d3da799599276805ae9eca3cff5

DOI: 10.1016/j.electacta.2016.01.127

Khatuntseva, E.A., Sherman, A.A., Tsvetkov, Y.E., Nifantiev, N.E.
Phenyl 2-azido-2-deoxy-1-selenogalactosides: a single type of glycosyl donor for the highly stereoselective synthesis of α- and β-2-azido-2-deoxy-d-galactopyranosides
(2016) Tetrahedron Letters, 57 (6), pp. 708-711. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955192470&partnerID=40&md5=86c9d0569d801c60fcfe991bfa81809e

DOI: 10.1016/j.tetlet.2016.01.013

Shashkov, A.S., Potekhina, N.V., Senchenkova, S.N., Evtushenko, L.I.
Teichoic, teichulosonic and teichuronic acids in the cell wall of Brevibacterium aurantiacum VKM Ac-2111T
(2016) Carbohydrate Research, 421, pp. 17-24. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84953319837&partnerID=40&md5=8d43d942be47c9d2ad478a6c074c758f

DOI: 10.1016/j.carres.2015.12.007

Kashin, A.S., Galkin, K.I., Khokhlova, E.A., Ananikov, V.P.
Direct observation of self-organized water-containing structures in the liquid phase and their influence on 5-(hydroxymethyl)furfural formation in ionic liquids
(2016) Angewandte Chemie — International Edition, 55 (6), pp. 2161-2166. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961285584&partnerID=40&md5=9af1f93ff66c2e4c3dd1233db1e4347f

DOI: 10.1002/anie.201510090

Kustov, L.M., Tarasov, A.L.
Fischer-Tropsch synthesis in a slurry mode using ionic liquids
(2016) Catalysis Communications, 75, pp. 42-44. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84950146302&partnerID=40&md5=1529544d997aefdc12c63f7cccd2b964

DOI: 10.1016/j.catcom.2015.12.003

Terent'ev, A.O., Vil', V.A., Gorlov, E.S., Nikishin, G.I., Pivnitsky, K.K., Adam, W.
Lanthanide-catalyzed oxyfunctionalization of 1,3-diketones, acetoacetic esters, and malonates by oxidative C-O coupling with malonyl peroxides
(2016) Journal of Organic Chemistry, 81 (3), pp. 810-823. Cited 2 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957598968&partnerID=40&md5=264541bde00d302babcd34afd8c7ccd6

DOI: 10.1021/acs.joc.5b02233

Vedenyapina, M.D., Sharipov, M.Yu., Terent'Ev, A.O., Skundin, A.M., Vedenyapin, A.A.
Kinetics and mechanism of the electrochemical reduction of [1,2-bis(tert-butylperoxy)ethyl]benzene under conditions of the in situ recovery of a platinum surface
(2016) Russian Journal of Physical Chemistry A, 90 (2), pp. 475-478. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84953439635&partnerID=40&md5=3280e5f3ee457fcd85a2597e53267153

DOI: 10.1134/S0036024416020333

Bakharev, V.V., Parfenov, V.E., Gidaspov, A.A., Selezneva, E.V., Baymuratov, M.R., Averkiev, B.B., Sheremetev, A.B.
A simple and convenient method for the synthesis of 1,3,5-triazine-nitrolic acids. the first X-ray investigation of Z-isomeric nitrolic acid
(2016) Heterocyclic Communications, 22 (1), pp. 7-10. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957952551&partnerID=40&md5=5b235c8578a5d6ff2cb8fcb453e9ac61

DOI: 10.1515/hc-2015-0218

Elinson, M.N., Ryzhkov, F.V., Korolev, V.A., Egorov, M.P.
Pot, atom and step-economic (PASE) synthesis of medicinally relevant spiro[oxindole-3,4′-pyrano[4,3-b]pyran] scaffold
(2016) Heterocyclic Communications, 22 (1), pp. 11-15. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957957873&partnerID=40&md5=01b89dd7e2d5292204c16c75b53bd690

DOI: 10.1515/hc-2015-0232

Guo, X., Senchenkova, S.N., SHashkov, A.S., Perepelov, A.V., Liu, B., Knirel, Y.A.
Structure and gene cluster of the o-antigen of Escherichia coli o96
(2016) Carbohydrate Research, 420, pp. 1-5. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84950128829&partnerID=40&md5=400173a936ebd06543ddf7c0b1ee738c

DOI: 10.1016/j.carres.2015.11.005

Sinditskii, V.P., Burzhava, A.V., Chernyi, A.N., Shmelev, D.S., Apalkova, V.N., Palysaeva, N.V., Sheremetev, A.B.
A comparative study of two difurazanyl ethers: Thermal and physico-chemical properties
(2016) Journal of Thermal Analysis and Calorimetry, 123 (2), pp. 1431-1438. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84954306436&partnerID=40&md5=c1d9ae9a1fb2d69c3f6121431b74f7c0

DOI: 10.1007/s10973-015-5048-4

Karelin, A.A., Tsvetkov, Y.E., Paulovičová, E., Paulovičová, L., Nifantiev, N.E.
A Blockwise Approach to the Synthesis of (1→2)-Linked Oligosaccharides Corresponding to Fragments of the Acid-Stable β-Mannan from the Candida albicans Cell Wall
(2016) European Journal of Organic Chemistry, 2016 (6), pp. 1173-1181. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959147367&partnerID=40&md5=3a2b23efb4c746cbd1c82214c4b37fe2

DOI: 10.1002/ejoc.201501464

Kozlov, V.V., Danilov, L.L.
Reversed-phase ion-pair high-performance liquid chromatography assay of polyprenyl diphosphate oligomer homologues
(2016) Journal of Separation Science, 39 (3), pp. 525-527. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960796166&partnerID=40&md5=5ce14f3cea0469e1c170afb4abb9563c

DOI: 10.1002/jssc.201501098

Komarova, B.S., Tsvetkov, Y.E., Nifantiev, N.E.
Design of α-Selective Glycopyranosyl Donors Relying on Remote Anchimeric Assistance
(2016) Chemical Record, 16 (1), pp. 488-506. Cited 2 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959221494&partnerID=40&md5=cd23322ff8f7ca50ba72586b2795fbc2

DOI: 10.1002/tcr.201500245

Krylov, I.B., Kompanets, M.O., Novikova, K.V., Opeida, I.O., Kushch, O.V., Shelimov, B.N., Nikishin, G.I., Levitsky, D.O., Terent'ev, A.O.
Well-Known Mediators of Selective Oxidation with Unknown Electronic Structure: Metal-Free Generation and EPR Study of Imide-N-oxyl Radicals
(2016) Journal of Physical Chemistry A, 120 (1), pp. 68-73. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955103012&partnerID=40&md5=59707867644903966d675300b0d38494

DOI: 10.1021/acs.jpca.5b10722

Golomidova, A.K., Kulikov, E.E., Prokhorov, N.S., Guerrero-Ferreira, R.C., Knirel, Y.A., Kostryukova, E.S., Tarasyan, K.K., Letarov, A.V.
Branched lateral tail fiber organization in T5-like bacteriophages DT57C and DT571/2 is revealed by genetic and functional analysis
(2016) Viruses, 8 (1), art. no. 26, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955609597&partnerID=40&md5=d9a7abb4515c93865c4730431ecb5296

DOI: 10.3390/v8010026

Barachevsky, V.A., Venidiktova, O.V., Kobeleva, O.I., Gorelik, A.M., Ayt, A.O., Krayushkin, M.M., Tameev, A.R., Sigeikin, G.I., Saveliev, M.A., Vasiluyk, G.T.
Multifunctional nanostructured photochromic photoswitches
(2016) IEEE-NANO 2015 — 15th International Conference on Nanotechnology, art. no. 7388999, pp. 358-361. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964329566&partnerID=40&md5=6952777f6d1b9c9b7398d0797d411dd2

DOI: 10.1109/NANO.2015.7388999

Ustyuzhanina, N.E., Bilan, M.I., Gerbst, A.G., Ushakova, N.A., Tsvetkova, E.A., Dmitrenok, A.S., Usov, A.I., Nifantiev, N.E.
Anticoagulant and antithrombotic activities of modified xylofucan sulfate from the brown alga Punctaria plantaginea
(2016) Carbohydrate Polymers, 136, art. no. 10404, pp. 826-833. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84943623670&partnerID=40&md5=97e8e413965bb4f18137d9489e308dc4

DOI: 10.1016/j.carbpol.2015.09.102

Schols, D., Ruchko, E.A., Lavrenov, S.N., Kachala, V.V., Nawrozkij, M.B., Babushkin, A.S.
Structural analogs of umifenovir 2*. The synthesis and antiHIV activity study of new regioisomeric (trans-2-phenylcyclopropyl)-1Н-indole derivatives
(2016) Chemistry of Heterocyclic Compounds, pp. 1-6. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84954481101&partnerID=40&md5=1cfd7ff5c20e3fbfb431e66d3fabb8bf

DOI: 10.1007/s10593-016-1807-9
DOCUMENT TYPE: Article in Press

Mikhaylov, A.A., Dilman, A.D., Novikov, R.A., Khoroshutina, Y.A., Struchkova, M.I., Arkhipov, D.E., Nelyubina, Y.V., Tabolin, A.A., Ioffe, S.L.
Tandem Pd-catalyzed C-C coupling/recyclization of 2-(2-bromoaryl)cyclopropane-1,1-dicarboxylates with primary nitro alkanes
(2016) Tetrahedron Letters, 57 (1), pp. 11-14. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84949921007&partnerID=40&md5=5d3fb945d140f2973ae54fc1528a6368

DOI: 10.1016/j.tetlet.2015.10.091

Kuznetsov, N.Yu., Tikhov, R.M., Godovikov, I.A., Khrustalev, V.N., Bubnov, Yu.N.
New enolate-carbodiimide rearrangement in the concise synthesis of 6-amino-2,3-dihydro-4-pyridinones from homoallylamines
(2016) Organic and Biomolecular Chemistry, 14 (18), pp. 4283-4298. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84966930556&partnerID=40&md5=bf79544bdc7feff6d56e6d47b488ec4c

DOI: 10.1039/c6ob00293e

Fershtat, L.L., Kulikov, A.S., Ananyev, I.V., Struchkova, M.I., Makhova, N.N.
New Method for the Synthesis and Reactivity of (5-R-1,3,4-Oxadiazol-2-yl)furoxans
(2016) Journal of Heterocyclic Chemistry, 53 (1), pp. 102-108. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84956709611&partnerID=40&md5=4786eda4d1d146777b2bbe02ad04ac5d

DOI: 10.1002/jhet.1940

Komarova, B.S., Orekhova, M.V., Tsvetkov, Y.E., Nifantiev, N.E.
Contribution of carbohydrate chemistry to assessment of the biological role of natural α-glucosides
(2016) Carbohydrate Chemistry, 41, pp. 187-237. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84951284171&partnerID=40&md5=d2140cf8d1b7a80d250aab71aa05689c

DOI: 10.1039/9781782620600-00187

Nazarov, A.K., Zavarzin, I.V., Nazarov, G.V., Aksenov, A.V., Levina, I.S.
Preparation and Bioavailability Evaluation of Micronized Steroidal Mecigestone Drug Substance
(2016) Pharmaceutical Chemistry Journal, 49 (10), pp. 706-710. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957556868&partnerID=40&md5=d4c041e58228b964ef0de78d31f49782

DOI: 10.1007/s11094-016-1357-6

Chizhkov, V.P., Boitsov, V.N.
Loss of thermodynamic work at the cascade stages during the separation of a multicomponent mixture of ideal gases
(2016) Russian Journal of Physical Chemistry A, 90 (1), pp. 226-232. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84949571044&partnerID=40&md5=ea734bacacd610aedd8184fc1efe20e4

DOI: 10.1134/S0036024416010064

Shirinian, V.Z., Lonshakov, D.V., Lvov, A.G., Kavun, A.M., Yadykov, A.V., Krayushkin, M.M.
Photo- and PH-switchable fluorescent diarylethenes based on 2,3-diarylcyclopent-2-en-1-ones with dialkylamino groups
(2016) Dyes and Pigments, 124, pp. 258-267. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84944205944&partnerID=40&md5=63ee9fd7e2d3a9360e25711fa28775da

DOI: 10.1016/j.dyepig.2015.09.027

Ananikov, V.P.
Do nanoparticles have a survival instinct?
(2016) Mendeleev Communications, 26 (1), pp. 1-2. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957066541&partnerID=40&md5=ab8e95d404aea0ad0b056ba87f6e3b52

DOI: 10.1016/j.mencom.2016.01.001

Zavelev, D.E., Chistyakov, A.V., Zhidomirov, G.M., Gubanov, M.A., Tsodikov, M.V., Moiseev, I.I.
Mechanism of the reductive dehydration of ethanol into C<inf>3+</inf> alkanes over the commercial alumina — Platinum catalyst AP-64
(2016) Kinetics and Catalysis, 57 (1), pp. 95-103. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962142351&partnerID=40&md5=a785ee7754966dd923710144d38d90aa

DOI: 10.1134/S0023158416010134

Ananikov, V., Liu, X., Schneider, U.
Catalysis to Build Molecular Complexity with Atomic Precision
(2016) Chemistry — An Asian Journal, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84968456934&partnerID=40&md5=5e3904deffbab232a815f8562288a3e8

DOI: 10.1002/asia.201501405
DOCUMENT TYPE: Article in Press

Galkin, K.I., Krivodaeva, E.A., Romashov, L.V., Zalesskiy, S.S., Kachala, V.V., Burykina, J.V., Ananikov, V.P.
Critical Influence of 5-Hydroxymethylfurfural Aging and Decomposition on the Utility of Biomass Conversion in Organic Synthesis
(2016) Angewandte Chemie — International Edition, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84973575848&partnerID=40&md5=326066d7917a37986de0e976d5ab8f98

DOI: 10.1002/anie.201602883
DOCUMENT TYPE: Article in Press

Kuchuk, E.A., Zaitsev, K.V., Karlov, S.S., Egorov, M.P., Churakov, A.V.
Crystal structure of 4,8-di-tert-butyl-6,6-dichloro-13-ethyl-2,10-dimethyl-13,14-dihydro-12H-dibenzo[d,i][1,3,7,2]dioxazasilecine toluene 0.25-solvate
(2016) Acta Crystallographica Section E: Crystallographic Communications, 71, pp. o1065-o1066. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955469528&partnerID=40&md5=aab0da5817e55323bdee8fa442848b2e

DOI: 10.1107/S2056989015023889

Karmanova, I.B., Firgang, S.I., Konyushkin, L.D., Khrustalev, V.N., Ignatov, A.V., Kuznetsov, L.A., Pinchuk, Y.A., Kozlov, I.A., Semenov, V.V.
Dill and parsley seed extracts in scale up synthesis of aminopolyalkoxybenzenes — Beneficial synthons for fused nitrogen polyalkoxyheterocycles
(2016) Mendeleev Communications, 26 (1), pp. 66-68. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84956914420&partnerID=40&md5=2064e1ed049545aa0feccf8b6a191e10

DOI: 10.1016/j.mencom.2016.01.026

Galkina, M.A., Bodrin, G.V., Goryunov, E.I., Goryunova, I.B., Sherstneva, A.S., Urmambetova, J.S., Kolotyrkina, N.G., Il'In, M.M., Brel, V.K., Kochetkov, K.A.
Regioselective aza-Michael addition of azoles to 4-(diphenylphosphoryl)but-3-en-2-one
(2016) Mendeleev Communications, 26 (1), pp. 75-76. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84956889031&partnerID=40&md5=03c447489f459e5d77524fc9c3715e3f

DOI: 10.1016/j.mencom.2016.01.029

Fershtat, L.L., Larin, A.A., Epishina, M.A., Ovchinnikov, I.V., Kulikov, A.S., Ananyev, I.V., Makhova, N.N.
Design of hybrid heterocyclic systems with a furoxanylpyridine core via tandem hetero-Diels-Alder/retro-Diels-Alder reactions of (1,2,4-triazin-3-yl)furoxans
(2016) RSC Advances, 6 (37), pp. 31526-31539. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962129216&partnerID=40&md5=c926f29eca542b5acac6ea09acea63b6

DOI: 10.1039/c6ra05110c

Sedykh, A.E., Gordeev, E.G., Pentsak, E.O., Ananikov, V.P.
Shielding the chemical reactivity using graphene layers for controlling the surface properties of carbon materials
(2016) Physical Chemistry Chemical Physics, 18 (6), pp. 4608-4616. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957555408&partnerID=40&md5=3f417342caeef53f292a223a42771063

DOI: 10.1039/c5cp05586e

Roshchina, T.M., Shoniya, N.K., Tegina, O.Y., Tkachenko, O.P., Kustov, L.M.
Physicochemical properties of surfaces of SBA-15 silicas, according to adsorption-static, gas-chromatographic, and IR spectroscopic data
(2016) Russian Journal of Physical Chemistry A, 90 (1), pp. 191-200. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84949599548&partnerID=40&md5=40d3b3c5800abde31695977aa8dcb5af

DOI: 10.1134/S0036024416010258

Mankaev, B.N., Zaitsev, K.V., Karlov, S.S., Egorov, M.P., Churakov, A.V.
Crystal structure of 2,6-bis(2-hydroxy-5-methylphenyl)-4-phenylpyridinium bromide dichloromethane hemisolvate hemihydrate
(2016) Acta Crystallographica Section E: Crystallographic Communications, 71, pp. o953-o954. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955505306&partnerID=40&md5=31b967c674b921142af252dfc16c8be0

DOI: 10.1107/S2056989015021386

Volkova, Y.A., Antonov, Y.S., Komkov, A.V., Scherbakov, A.M., Shashkov, A.S., Menchikov, L.G., Chernoburova, E.I., Zavarzin, I.V.
Access to steroidal pyridazines via modified thiohydrazides
(2016) RSC Advances, 6 (49), pp. 42863-42868. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969246449&partnerID=40&md5=2921d67317bb405def5704fc9ff41654

DOI: 10.1039/c6ra06881b

Gidaspov, A.A., Zalomlenkov, V.A., Bakharev, V.V., Parfenov, V.E., Yurtaev, E.V., Struchkova, M.I., Palysaeva, N.V., Suponitsky, K.Y., Lempert, D.B., Sheremetev, A.B.
Novel trinitroethanol derivatives: High energetic 2-(2,2,2-trinitroethoxy)-1,3,5-triazines
(2016) RSC Advances, 6 (41), pp. 34921-34934. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84966378438&partnerID=40&md5=33499c22072c41078afde2260ccbdf86

DOI: 10.1039/c6ra05826d

Lvov, A.G., Bulich, E.Yu., Metelitsa, A.V., Shirinian, V.Z.
Facile synthesis of photoactive diaryl(hetaryl)cyclopentenes by ionic hydrogenation
(2016) RSC Advances, 6 (64), pp. 59016-59020. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84976359364&partnerID=40&md5=68108bf2bce50cd29a83650435942509

DOI: 10.1039/c6ra11791k

Rodygin, K.S., Werner, G., Kucherov, F.A., Ananikov, V.P.
Calcium Carbide: A Unique Reagent for Organic Synthesis and Nanotechnology
(2016) Chemistry — An Asian Journal, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969402652&partnerID=40&md5=e3c3d90119e6a5b47662d3f9eb8981d3

DOI: 10.1002/asia.201501323
DOCUMENT TYPE: Article in Press

Sedenkova, K.N., Averina, E.B., Grishin, Y.K., Andriasov, K.S., Stepanova, S.A., Roznyatovsky, V.A., Kutateladze, A.G., Rybakov, V.B., Albov, D.V., Kuznetsova, T.S., Zefirov, N.S.
Beyond the Dimer and Trimer: Tetraspiro[2.1.25.1.29.1.213.13] hexadecane-1,3,5,7-tetraone-the Cyclic Tetramer of Carbonylcyclopropane
(2016) Chemistry — A European Journal, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84976209164&partnerID=40&md5=21a9668909732b1e9d9eadb33ac7e6c6

DOI: 10.1002/chem.201600140
DOCUMENT TYPE: Article in Press

Elinson, M.N., Vereshchagin, A.N., Ryzhkov, F.V.
Catalysis of Cascade and Multicomponent Reactions of Carbonyl Compounds and C-H Acids by Electricity
(2016) Chemical Record, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84973931763&partnerID=40&md5=ea04d96e288f4b0bdec48c75e897792a

DOI: 10.1002/tcr.201600044
DOCUMENT TYPE: Article in Press

Varlamov, A.V., Guranova, N.I., Novikov, R.A., Ilyushenkova, V.V., Khrustalev, V.N., Baleeva, N.S., Borisova, T.N., Voskressensky, L.G.
Synthesis of novel fluorescent 12a-aryl substituted indoxylisoquinolines via aryne-induced domino process
(2016) RSC Advances, 6 (15), pp. 12642-12646. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957106745&partnerID=40&md5=c7ad596fc309571bcdd8c582cf1782a5

DOI: 10.1039/c5ra25323c

Gvozdev, V.D., Shavrin, K.N., Egorov, M.P., Nefedov, O.M.
Stereoselective one-pot synthesis of (1Z)- and (1E)-1-arylmethylidene-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles by cyclization of alk-4-ynals with o-diaminobenzene
(2016) Mendeleev Communications, 26 (1), pp. 3-5. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957070783&partnerID=40&md5=68f6ccb3de73331ef23838d7e4b46b82

DOI: 10.1016/j.mencom.2016.01.002

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
(2016) Journal of Heterocyclic Chemistry, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961751206&partnerID=40&md5=8e582dd87f1e4fcbd08a7b63792e9494

DOI: 10.1002/jhet.2621
DOCUMENT TYPE: Article in Press

Pivkina, A.N., Muravyev, N.V., Monogarov, K.A., Fomenkov, I.V., Schoonman, J.
Catalysis of HMX Decomposition and Combustion: Defect Chemistry Approach
(2016) Energetic Nanomaterials: Synthesis, Characterization, and Application, pp. 193-230. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84966775461&partnerID=40&md5=8295a674c8efd2ce9a9694ed5e9e5d91

DOI: 10.1016/B978-0-12-802710-3.00009-X

Menchikov, L.G., Nefedov, O.M.
Spiro[2.4]hepta-4,6-dienes: Synthesis and application in organic synthesis
(2016) Russian Chemical Reviews, 85 (3), pp. 205-225. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84963543221&partnerID=40&md5=2fbce4dcce86050a697677d071af3be2

DOI: 10.1070/RCR4600

Tsivadze, A.Y., Aksyutin, O.E., Ishkov, A.G., Fomkin, A.A., Men’shchikov, I.E., Pribylov, A.A., Isaeva, V.I., Kustov, L.M., Shkolin, A.V., Strizhenov, E.M.
Adsorption of methane on an MOF-199 organometallic framework structure at high pressures in the range of supercritical temperatures
(2016) Protection of Metals and Physical Chemistry of Surfaces, 52 (1), pp. 24-29. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955471886&partnerID=40&md5=5c36571affe54d284ca76523708b0393

DOI: 10.1134/S2070205116010263

Tabolin, A.A., Ioffe, S.L.
Small Ring Compounds and N-oxides: Cycloadditions and Related Processes
(2016) Israel Journal of Chemistry, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959155778&partnerID=40&md5=f85d60bd197567d9dd28dd97ed62f1df

DOI: 10.1002/ijch.201500082
DOCUMENT TYPE: Article in Press

Vedenyapina, M.D., Stopp, P., Weichgrebe, D., Vedenyapin, A.A.
Adsorption of diclofenac sodium from aqueous solutions on activated carbon
(2016) Solid Fuel Chemistry, 50 (1), pp. 46-50. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961601692&partnerID=40&md5=c0a13245ec18cbf702fceca486fc1c52

DOI: 10.3103/S0361521916010109

Yashunsky, D.V., Tsvetkov, Y.E., Grachev, A.A., Chizhov, A.O., Nifantiev, N.E.
Synthesis of 3-aminopropyl glycosides of linear β-(1→3)-d-glucooligosaccharides
(2016) Carbohydrate Research, 419, pp. 1-10. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84947563167&partnerID=40&md5=fab55b7bc6743ab7b750381d3880f702

DOI: 10.1016/j.carres.2015.10.012

Botavina, M.A., Agafonov, Y.A., Gaidai, N.A., Groppo, E., Cortés Corberán, V., Lapidus, A.L., Martra, G.
Towards efficient catalysts for the oxidative dehydrogenation of propane in the presence of CO<inf>2</inf>: Cr/SiO<inf>2</inf> systems prepared by direct hydrothermal synthesis
(2016) Catalysis Science and Technology, 6 (3), pp. 840-850. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957873559&partnerID=40&md5=eb5b72b57efc0d7259668ba2a4b009ed

DOI: 10.1039/c5cy00998g

Rodygin, K.S., Ananikov, V.P.
An efficient metal-free pathway to vinyl thioesters with calcium carbide as the acetylene source
(2016) Green Chemistry, 18 (2), pp. 482-486. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955319557&partnerID=40&md5=0b1d4eae80baf95483a812f61b78298e

DOI: 10.1039/c5gc01552a

Zhang, R., Eckert, T., Lütteke, T., Hanstein, S., Scheidig, A., Bonvin, A.M.J.J., Nifantiev, N.E., Kožár, T., Schauer, R., Enani, M.A., Siebert, H.-C.
Structure-function relationships of antimicrobial peptides and proteins with respect to contact molecules on pathogen surfaces
(2016) Current Topics in Medicinal Chemistry, 16 (1), pp. 89-98. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84947750006&partnerID=40&md5=a74dc78e8f9fd71273acc0019372149d

Galkin, K.I., Ananikov, V.P.
Alkynes as a versatile platform for construction of chemical molecular complexity and realization of molecular 3D printing
(2016) Russian Chemical Reviews, 85 (3), pp. 226-247. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84963576465&partnerID=40&md5=b344d5b195c347287d7907e7ddedf6a6

DOI: 10.1070/RCR4611

 Zdorovenko, E.L., Kadykova, A.A., Varbanets, L.D., Shashkov, A.S., Kiprianova, E.A., Brovarskaya, O.S., Knirel, Y.A.

Structure of the O-specific polysaccharides of Pseudomonas chlororaphis subsp. chlororaphis UCM B-106
(2016) Carbohydrate Research, 433, pp. 1-4. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978219417&partnerID=40&md5=764a50385be432d025f487bb78c25044

DOI: 10.1016/j.carres.2016.06.013
DOCUMENT TYPE: Article

Senchenkova, S.N., Guo, X., Filatov, A.V., Perepelov, A.V., Liu, B., Shashkov, A.S., Knirel, Y.A.
Structure elucidation and gene cluster characterization of the O-antigen of Escherichia coli O80
(2016) Carbohydrate Research, 432, pp. 83-87. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978880249&partnerID=40&md5=71ffc47dd91d71f03903ceafc97b8cc9

DOI: 10.1016/j.carres.2016.07.011

Fedorov, O.V., Levin, V.V., Volodin, A.D., Struchkova, M.I., Korlyukov, A.A., Dilman, A.D.
Synthesis of difluorosubstituted six-membered nitronates via an addition/substitution cascade
(2016) Tetrahedron Letters, 57 (32), pp. 3639-3642. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978863405&partnerID=40&md5=993fd388a63bd2dac35768b563055a6d

DOI: 10.1016/j.tetlet.2016.06.135

Trifonov, A.L., Zemtsov, A.A., Levin, V.V., Struchkova, M.I., Dilman, A.D.
Nucleophilic Difluoromethylation Using (Bromodifluoromethyl)trimethylsilane
(2016) Organic Letters, 18 (14), pp. 3458-3461. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978730683&partnerID=40&md5=e4f5c997bba6d98590171adedd224241

DOI: 10.1021/acs.orglett.6b01641

Keshtov, M.L., Konstantinov, I.O., Krayushkin, M.M., Kuklin, S.A., Masoud, S.M., Osipov, S.N., Khokhlov, A.R.
New electron-accepting quinoxalinothiadiazole-containing heterocycles as promising building blocks for organic optoelectronic devices
(2016) Doklady Chemistry, 468 (2), pp. 202-207. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978435123&partnerID=40&md5=841197974fb79a6b6fc146af6353acde

DOI: 10.1134/S0012500816060069

Isaeva, V.I., Kustov, L.M.
Metal-Organic Frameworks and Related Materials: Miles to Go
(2016) Zeolites and Zeolite-like Materials, pp. 33-109. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978633704&partnerID=40&md5=7b13ae3817c28f13a7dacead65735b9d

DOI: 10.1016/B978-0-444-63506-8.00002-1
DOCUMENT TYPE: Book Chapter

Sels, B.F., Kustov, L.M.
Zeolites and Zeolite-like Materials
(2016) Zeolites and Zeolite-like Materials, pp. 1-459. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978764820&partnerID=40&md5=3e94005ec2d403eb5d12547b3fdc36e2

Sels, B.F., Kustov, L.M.
Preface
(2016) Zeolites and Zeolite-like Materials, pp. xiii-xiv. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978646289&partnerID=40&md5=fc56f1766d87cb76f8691115dd07f28c

DOI: 10.1016/B978-0-444-63506-8.10000-X

Kustov, L.M., Kuperman, A., Kustov, A.
Further Steps of Zeolites Toward Industrial Applications: A Short-Range Outlook
(2016) Zeolites and Zeolite-like Materials, pp. 309-369. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978742651&partnerID=40&md5=1e515f2f121330fbc4a812ae13e60c5d

DOI: 10.1016/B978-0-444-63506-8.00009-4

Kustov, L.M., Furman, D.B., Barkova, A.P.
Metathesis of C<inf>5</inf>–C<inf>8</inf> Terminal Olefins on Re<inf>2</inf>O<inf>7</inf>/Al<inf>2</inf>O<inf>3</inf> Catalysts
(2016) Catalysis Letters, pp. 1-7. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84977996260&partnerID=40&md5=471063574930d69f604aaf39c05cbad5

DOI: 10.1007/s10562-016-1698-5
DOCUMENT TYPE: Article in Press

Klenov, M.S., Guskov, A.A., Anikin, O.V., Churakov, A.M., Strelenko, Y.A., Fedyanin, I.V., Lyssenko, K.A., Tartakovsky, V.A.
Synthesis of Tetrazino-tetrazine 1,3,6,8-Tetraoxide (TTTO)
(2016) Angewandte Chemie — International Edition, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978827381&partnerID=40&md5=c91e87d421d6aea8df5eed8a9f518167

DOI: 10.1002/anie.201605611
DOCUMENT TYPE: Article in Press

Platonov, D.N., Belyy, A.Y., Ananyev, I.V., Tomilov, Y.V.
Synthesis of 1,2,3,4,5,6,7-Heptasubstituted Cycloheptatrienes through Cycloaddition Reactions of Substituted Cyclopentadienones
(2016) European Journal of Organic Chemistry, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978736613&partnerID=40&md5=88fa6d63f341d94a50c8e62cfde613f1

DOI: 10.1002/ejoc.201600516
DOCUMENT TYPE: Article in Press

 Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Tsvetkova, E.A., Shashkov, A.S., Stonik, V.A., Nifantiev, N.E., Usov, A.I.
Structural characterization of fucosylated chondroitin sulfates from sea cucumbers Apostichopus japonicus and Actinopyga mauritiana
(2016) Carbohydrate Polymers, 153, pp. 399-405.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84980349528&partnerID=40&md5=20c8ea2ae1e8fa0472f31363c3c0b726

DOI: 10.1016/j.carbpol.2016.07.076


Sheveleva, E.E., Pimenov, V.G., Pikulin, I.V., Sakharov, A.M.
The formation of ultralow-density microcellular diane-formaldehyde gels and aerogels
(2016) Polymer Science — Series B, 58 (2), pp. 173-182.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979642321&partnerID=40&md5=f1910a73c3e316b2422ea7a604d4b128

DOI: 10.1134/S1560090416020081


Kalenchuk, A.N., Bogdan, V.I., Bogorodskii, S.E., Kustov, L.M.
Effect of the structure of the ortho, meta, and para isomers of perhydroterphenyl on their reactivity in heterogeneous catalytic dehydrogenation
(2016) Kinetics and Catalysis, 57 (2), pp. 219-223.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979641024&partnerID=40&md5=63c4eeda7642eec2df68931919e62eb7

DOI: 10.1134/S0023158416020038


Isaeva, V.I., Eliseev, O.L., Kazantsev, R.V., Chernyshev, V.V., Davydov, P.E., Saifutdinov, B.R., Lapidus, A.L., Kustov, L.M.
Fischer-Tropsch synthesis over MOF-supported cobalt catalysts (Co@MIL-53(Al))
(2016) Dalton Transactions, 45 (30), pp. 12006-12014.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979894406&partnerID=40&md5=aa1917f6dce854c38f3dbd895288d879

DOI: 10.1039/c6dt01394e


Toukach, P.V., Egorova, K.S.
Carbohydrate structure database merged from bacterial, archaeal, plant and fungal parts
(2016) Nucleic Acids Research, 44 (D1), pp. D1229-D1236.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979545696&partnerID=40&md5=f1f164b1b15a8b74f33df44ac8e05e61

DOI: 10.1093/nar/gkv840


Keshtov, M.L., Kuklin, S.A., Radychev, N.A., Ostapov, I.E., Nikolaev, A.Y., Konstantinov, I.O., Krayushkin, M.M., Koukaras, E.N., Sharma, A., Sharma, G.D.
Synthesis of new D-A1-D-A2 type low bandgap terpolymers based on different thiadiazoloquinoxaline acceptor units for efficient polymer solar cells
(2016) RSC Advances, 6 (75), pp. 71232-71244.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979953929&partnerID=40&md5=d61be55857aff091dbbea75f5748ec24

DOI: 10.1039/c6ra14537j


 Yashunsky, D.V., Tsvetkov, Y.E., Nifantiev, N.E.

Synthesis of 3-aminopropyl glycoside of branched β-(1 → 3)-D-glucooctaoside
(2016) Carbohydrate Research, 436, pp. 25-30. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994747486&doi=10.1016%2fj.carres.2016.11.005&partnerID=40&md5=fcfc6696d16bfcdfb2546c66669fc968

DOI: 10.1016/j.carres.2016.11.005

Gerbst, A.G., Krylov, V.B., Argunov, D.A., Solovev, A.S., Dmitrenok, A.S., Shashkov, A.S., Nifantiev, N.E.
Ring distortion in pyranosides caused by per-O-sulfation
(2016) Carbohydrate Research, 436, pp. 20-24. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994311278&doi=10.1016%2fj.carres.2016.10.011&partnerID=40&md5=e62b0b3987007b1f7fa19cf01066216b

DOI: 10.1016/j.carres.2016.10.011

Perepelov, A.V., Wang, Q., Filatov, A.V., Xia, X., Shashkov, A.S., Weintraub, A., Widmalm, G., Wang, L., Knirel, Y.A.
Corrigendum to “Structures and gene clusters of the closely related O-antigens of Escherichia coli O46 and O134, both containing D-glucuronoyl-D-allothreonine” (Carbohydrate Research (2015) 409 (20–24) (S0008621515000981) (10.1016/j.carres.2015.03.014))
(2016) Carbohydrate Research, 436, p. 54. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85004038649&doi=10.1016%2fj.carres.2016.11.014&partnerID=40&md5=0e8cbcca7c6b362282b4e6c6fce10e66

DOI: 10.1016/j.carres.2016.11.014

Perepelov, A.V., Guo, X., Senchenkova, S.N., Shashkov, A.S., Liu, B., Knirel, Y.A.
Structure elucidation and analysis of biosynthesis genes of the O-antigen of Escherichia coli O131 containing N-acetylneuraminic acid
(2016) Carbohydrate Research, 436, pp. 41-44. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994728019&doi=10.1016%2fj.carres.2016.11.003&partnerID=40&md5=a9d15dc7875471be80f13a6b95ccb322

DOI: 10.1016/j.carres.2016.11.003

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
(2016) Synlett, . Article in Press. 
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

Shirinian, V.Z., Lvov, A.G., Yadykov, A.V., Yaminova, L.V., Kachala, V.V., Markosyan, A.I.
Triaryl-Substituted Divinyl Ketones Cyclization: Nazarov Reaction versus Friedel-Crafts Electrophilic Substitution
(2016) Organic Letters, 18 (24), pp. 6260-6263. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006506892&doi=10.1021%2facs.orglett.6b03023&partnerID=40&md5=ac6e34ce838c6b178b804f3367fbe290

DOI: 10.1021/acs.orglett.6b03023

Fershtat, L.L., Epishina, M.A., Ovchinnikov, I.V., Struchkova, M.I., Romanova, A.A., Ananyev, I.V., Makhova, N.N.
Side-chain prototropic tautomerism of 4-hydroxyfuroxans in methylation reactions
(2016) Tetrahedron Letters, 57 (50), pp. 5685-5689. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996538261&doi=10.1016%2fj.tetlet.2016.11.023&partnerID=40&md5=4201f213efab85817bf39ce892bf7b43

DOI: 10.1016/j.tetlet.2016.11.023

Pavlova, A.S., Ivanova, O.A., Chagarovskiy, A.O., Stebunov, N.S., Orlov, N.V., Shumsky, A.N., Budynina, E.M., Rybakov, V.B., Trushkov, I.V.
Domino Staudinger/aza-Wittig/Mannich Reaction: An Approach to Diversity of Di- and Tetrahydropyrrole Scaffolds
(2016) Chemistry — A European Journal, 22 (50), pp. 17967-17971. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996917543&doi=10.1002%2fchem.201604056&partnerID=40&md5=ca57d1bbc68eb5670138d60460d21f9c

DOI: 10.1002/chem.201604056

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
(2016) Synlett, . Article in Press. 
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

Muravyev, N.V., Bragin, A.A., Monogarov, K.A., Nikiforova, A.S., Korlyukov, A.A., Fomenkov, I.V., Shishov, N.I., Pivkina, A.N.
5-Amino-3,4-dinitropyrazole as a Promising Energetic Material
(2016) Propellants, Explosives, Pyrotechnics, 41 (6), pp. 999-1005. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994740511&doi=10.1002%2fprep.201600068&partnerID=40&md5=b70ac4f0c9b6ef61b1dde3ac5f8f5711

DOI: 10.1002/prep.201600068

Dorokhov, V.S., Permyakov, E.A., Nikulshin, P.A., Maximov, V.V., Kogan, V.M.
Experimental and computational study of syngas and ethanol conversion mechanisms over K-modified transition metal sulfide catalysts
(2016) Journal of Catalysis, 344, pp. 841-853. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994888144&doi=10.1016%2fj.jcat.2016.08.005&partnerID=40&md5=2ec3690d46f4abdb1244cb1fc7ea77ee

DOI: 10.1016/j.jcat.2016.08.005

Sukhova, E.V., Yashunsky, D.V., Tsvetkov, Y.E., Nifantiev, N.E.
The synthesis of the phosphate-bridged tetrasaccharide representing the repeating unit of the capsular polysaccharide of Streptococcus pneumoniae serotype 6B
(2016) Phosphorus, Sulfur and Silicon and the Related Elements, 191 (11-12), pp. 1543-1544. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84992561236&doi=10.1080%2f10426507.2016.1213251&partnerID=40&md5=540b86682d315666c9d57768584167ff

DOI: 10.1080/10426507.2016.1213251

Senchenkova, S.N., Guo, X., Naumenko, O.I., Shashkov, A.S., Perepelov, A.V., Liu, B., Knirel, Y.A.
Structure and genetics of the O-antigens of Escherichia coli O182–O187
(2016) Carbohydrate Research, 435, pp. 58-67. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989337858&doi=10.1016%2fj.carres.2016.09.014&partnerID=40&md5=a65c93937adbdaff289992d5c80f9a1f

DOI: 10.1016/j.carres.2016.09.014

Kachalov, V.V., Lavrenov, V.A., Lishchiner, I.I., Malova, O.V., Tarasov, A.L., Zaichenko, V.M.
Scientific bases of biomass processing into basic component of aviation fuel
(2016) Journal of Physics: Conference Series, 774 (1), art. no. 012136, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85007039308&doi=10.1088%2f1742-6596%2f774%2f1%2f012136&partnerID=40&md5=d241f2c8789a405dff9d5cdfe6d3b066

DOI: 10.1088/1742-6596/774/1/012136

Eremin, D.B., Ananikov, V.P.
Understanding active species in catalytic transformations: From molecular catalysis to nanoparticles, leaching, "Cocktails" of catalysts and dynamic systems
(2016) Coordination Chemistry Reviews, . Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009834476&doi=10.1016%2fj.ccr.2016.12.021&partnerID=40&md5=3ff8e4246ca214e5e2fc0a03bd88bc8d

DOI: 10.1016/j.ccr.2016.12.021

Zavozin, A.G., Simirskaya, N.I., Nelyubina, Y.V., Zlotin, S.G.
Novel di- and tetra(pyrazolyl)bipyridine ligands and their Co (II)-complexes for electrochemical applications
(2016) Tetrahedron, 72 (47), pp. 7552-7556. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991268647&doi=10.1016%2fj.tet.2016.10.006&partnerID=40&md5=01a4566c68dbe8571c7588259ace6c7c

DOI: 10.1016/j.tet.2016.10.006

Semakin, A.N., Kokuev, A.O., Nelyubina, Y.V., Sukhorukov, A.Yu., Zhmurov, P.A., Ioffe, S.L., Tartakovsky, V.A.
Construction of bis-, tris- and tetrahydrazones by addition of azoalkenes to amines and ammonia
(2016) Beilstein Journal of Organic Chemistry, 12, pp. 2471-2477. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85000956336&doi=10.3762%2fbjoc.12.241&partnerID=40&md5=88b44e8ed828e1bb77862420e0681819

DOI: 10.3762/bjoc.12.241

Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Tsvetkova, E.A., Shashkov, A.S., Stonik, V.A., Nifantiev, N.E., Usov, A.I.
Structural characterization of fucosylated chondroitin sulfates from sea cucumbers Apostichopus japonicus and Actinopyga mauritiana
(2016) Carbohydrate Polymers, 153, pp. 399-405. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84980349528&doi=10.1016%2fj.carbpol.2016.07.076&partnerID=40&md5=d9b28e24f1d2d93fca3b5f86746d1e72

DOI: 10.1016/j.carbpol.2016.07.076

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
(2016) Tetrahedron Letters, . Article in Press. 
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

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
(2016) Tetrahedron Letters, . Article in Press. 
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

Novikov, R.A., Borisov, D.D., Tomilov, Y.V.
The effect of ligands on the change of diastereoselectivity dimerization of 2-(naphthyl-1)cyclopropanedicarboxylate in the presence of GaCl<inf>3</inf>
(2016) Arkivoc, 2016 (5), pp. 362-374. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994765299&doi=10.3998%2fark.5550190.p009.860&partnerID=40&md5=add37f3f78fc310d079172e12c36f0ac

DOI: 10.3998/ark.5550190.p009.860

Bastrakov, M.A., Starosotnikov, A.M., Pavlov, A.A., Dalinger, I.L., Shevelev, S.A.
Synthesis of novel polycyclic heterosystems from 5-nitro[1,2,5]selenadiazolo[3,4-e]benzofuroxans
(2016) Chemistry of Heterocyclic Compounds, pp. 1-4. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994476109&doi=10.1007%2fs10593-016-1950-3&partnerID=40&md5=007025cfb63ffb9f38f41ba2762006c7

DOI: 10.1007/s10593-016-1950-3

Lvov, A.G., Shirinyan, V.Z.
Photoinduced Rearrangements of Diarylethenes
(2016) Chemistry of Heterocyclic Compounds, pp. 1-8. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994472165&doi=10.1007%2fs10593-016-1946-z&partnerID=40&md5=2a6ce701c8c95ee6595b5c3fffe67631

DOI: 10.1007/s10593-016-1946-z

Argunov, D.A., Krylov, V.B., Nifantiev, N.E.
The Use of Pyranoside-into-Furanoside Rearrangement and Controlled O(5) → O(6) Benzoyl Migration as the Basis of a Synthetic Strategy to Assemble (1→5)- and (1→6)-Linked Galactofuranosyl Chains
(2016) Organic Letters, 18 (21), pp. 5504-5507. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994585588&doi=10.1021%2facs.orglett.6b02735&partnerID=40&md5=426cd880d0b11cf062cf0e6528d5bb08

DOI: 10.1021/acs.orglett.6b02735

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
(2016) Synlett, . Article in Press. 
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

Kokorekin, V.A., Solomatin, Y.A., Gening, M.L., Petrosyan, V.A.
Electrochemical S<inf>N</inf>H(An) functionalization of 1,2- and 1,4-dihydroxybenzenes
(2016) Mendeleev Communications, 26 (6), pp. 540-542. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996921091&doi=10.1016%2fj.mencom.2016.11.028&partnerID=40&md5=abf0f4a104c55dfba8af00cbdcb2eb8e

DOI: 10.1016/j.mencom.2016.11.028

Sheremetev, A.B., Korolev, V.L., Potemkin, A.A., Aleksandrova, N.S., Palysaeva, N.V., Hoang, T.H., Sinditskii, V.P., Suponitsky, K.Y.
Oxygen-Rich 1,2,4-Triazolo[3,4-d]-1,2,4-triazolo[3,4-f]furazano[3,4-b]pyrazines as Energetic Materials
(2016) Asian Journal of Organic Chemistry, 5 (11), pp. 1388-1397. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988813701&doi=10.1002%2fajoc.201600386&partnerID=40&md5=ffc563227675323579979081418e3222

DOI: 10.1002/ajoc.201600386

Rassolov, A.V., Markov, P.V., Bragina, G.O., Baeva, G.N., Mashkovskii, I.S., Yakushev, I.A., Vargaftik, M.N., Stakheev, A.Y.
Catalytic properties of nanostructured Pd–Ag catalysts in the liquid-phase hydrogenation of terminal and internal alkynes
(2016) Kinetics and Catalysis, 57 (6), pp. 853-858. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84999664642&doi=10.1134%2fS0023158416060124&partnerID=40&md5=5a986b5db71f77e22730eb6b28e8a2ce

DOI: 10.1134/S0023158416060124

Shershnev, V.A., Bogdanova, L.M., Golubeva, N.D., Yuryeva, E.A., Sanina, N.A., Shirinyan, V.Z., Aldoshin, S.M., Dzhardimalieva, G.I.
Photochromic and Magnetic Nanocomposites Based on Epoxy and Polycarbonate Matrices
(2016) Journal of Inorganic and Organometallic Polymers and Materials, 26 (6), pp. 1320-1327. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989162878&doi=10.1007%2fs10904-016-0450-3&partnerID=40&md5=74556d9210b68235f0241d4988e38cc7

DOI: 10.1007/s10904-016-0450-3

Lebedeva, O., Kultin, D., Root, N., Guseynov, F., Dunaev, S., De Melo, F., Kustov, L.
First successful synthesis of polypyridines in ionic liquid: Role of 1‐butyl-3-methylimidazolium tetrafluoroborate as electrolyte
(2016) Synthetic Metals, 221, pp. 268-274. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84993961106&doi=10.1016%2fj.synthmet.2016.09.013&partnerID=40&md5=36deecfa5c41e0320511ccbe98ffd5f2

DOI: 10.1016/j.synthmet.2016.09.013

Sukhanova, A.A., Nelyubina, Y.V., Zlotin, S.G.
Asymmetric synthesis of 3-prenyl-substituted pyrrolidin-2-ones
(2016) Mendeleev Communications, 26 (6), pp. 471-473. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996671169&doi=10.1016%2fj.mencom.2016.11.003&partnerID=40&md5=f2cf8d9f3c2aa64259fe06a68a230363

DOI: 10.1016/j.mencom.2016.11.003

Chudov, K.A., Levchenko, K.S., Barachevskii, V.A., Valova, T.M., Grebennikov, E.P., Shmelin, P.S., Poroshin, N.O., Adamov, G.E., Yarovenko, V.N., Krayushkin, M.M.
3-Acyl-2-furylthiochromones: a new family of compounds with photoinduced fluorescence
(2016) Mendeleev Communications, 26 (6), pp. 521-523. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996848231&doi=10.1016%2fj.mencom.2016.11.021&partnerID=40&md5=1dd78ef8d85fda0694d340678385587d

DOI: 10.1016/j.mencom.2016.11.021

Markov, P.V., Bragina, G.O., Rassolov, A.V., Baeva, G.N., Mashkovsky, I.S., Murzin, V.Y., Zubavichus, Y.V., Stakheev, A.Y.
Pd–Cu catalyst prepared from heterobimetallic PdCu<inf>2</inf>(OAc)<inf>6</inf>: an XRD-EXAFS study and activity/selectivity in the liquid-phase hydrogenation of a C≡C bond
(2016) Mendeleev Communications, 26 (6), pp. 502-504. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84997501275&doi=10.1016%2fj.mencom.2016.11.014&partnerID=40&md5=b4770b8cab4c8c3a86e57b599baf6f74

DOI: 10.1016/j.mencom.2016.11.014

Ustyuzhanina, N.E., Fershtat, L.L., Gening, M.L., Nifantiev, N.E., Makhova, N.N.
New insight into the antiaggregant activity of furoxans
(2016) Mendeleev Communications, 26 (6), pp. 513-515. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84997207236&doi=10.1016%2fj.mencom.2016.11.018&partnerID=40&md5=c2eb14b218f12186d11688d2449e804c

DOI: 10.1016/j.mencom.2016.11.018

Shved, A.S., Tabolin, A.A., Novikov, R.A., Nelyubina, Y.V., Timofeev, V.P., Ioffe, S.L.
Six-Membered Cyclic Nitroso Acetals: Synthesis and Studies of the Nitrogen Inversion Process of N-Silyloxy-3,6-dihydro-2H-1,2-oxazines
(2016) European Journal of Organic Chemistry, 2016 (33), pp. 5569-5578. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84995946831&doi=10.1002%2fejoc.201600952&partnerID=40&md5=36a0a83801a3ec569dc63505661ddc38

DOI: 10.1002/ejoc.201600952

Yuzbashev, T.V., Bondarenko, P.Y., Sobolevskaya, T.I., Yuzbasheva, E.Y., Laptev, I.A., Kachala, V.V., Fedorov, A.S., Vybornaya, T.V., Larina, A.S., Sineoky, S.P.
Metabolic evolution and 13C flux analysis of a succinate dehydrogenase deficient strain of Yarrowia lipolytica
(2016) Biotechnology and Bioengineering, 113 (11), pp. 2425-2432. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988939378&doi=10.1002%2fbit.26007&partnerID=40&md5=f994045ebc7199506ccaf288d75a3779

DOI: 10.1002/bit.26007

Greish, A.A., Finashina, E.D., Tkachenko, O.P., Shuvalova, E.V., Kustov, L.M.
Synthesis of dimethyl carbonate from methanol and CO<inf>2</inf> on the SnO<inf>2</inf>/Al<inf>2</inf>O<inf>3</inf>-based catalyst
(2016) Mendeleev Communications, 26 (6), pp. 497-499. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84997327893&doi=10.1016%2fj.mencom.2016.11.012&partnerID=40&md5=e3c47b055f36cf1acf5b703b8a76952a

DOI: 10.1016/j.mencom.2016.11.012

Kustov, L.M., Abramenko, N.B.
Study of ecotoxicity of silver nanoparticles using algae
(2016) Russian Journal of Physical Chemistry A, 90 (11), pp. 2217-2220. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991670339&doi=10.1134%2fS0036024416110121&partnerID=40&md5=fcbc6548784e1f4ea77d186f43f88cc4

DOI: 10.1134/S0036024416110121

Vedenyapina, M.D., Ubushieva, G.T., Kuznetsov, V.V., Makhova, N.N., Vedenyapin, A.A.
Anodic dissolution of gold in a solution of 1,3-diaminopropane with the formation of a cathodic deposit and a colloidal solution of Au
(2016) Russian Journal of Physical Chemistry A, 90 (11), pp. 2312-2315. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991716112&doi=10.1134%2fS0036024416110297&partnerID=40&md5=89f026aef16385a469572fd1fc628d61

DOI: 10.1134/S0036024416110297

Rassolov, A.V., Markov, P.V., Bragina, G.O., Baeva, G.N., Krivoruchenko, D.S., Mashkovskii, I.S., Yakushev, I.A., Vargaftik, M.N., Stakheev, A.Y.
Formation of Pd–Ag nanoparticles in supported catalysts based on the heterobimetallic complex PdAg<inf>2</inf>(OAc)<inf>4</inf>(HOAc)<inf>4</inf>
(2016) Kinetics and Catalysis, 57 (6), pp. 859-865. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84999791813&doi=10.1134%2fS0023158416060112&partnerID=40&md5=a74b23360abdcb3d1ac67d56ffec87b0

DOI: 10.1134/S0023158416060112

Drzewiecka, D., Arbatsky, N.P., Kondakova, A.N., Shashkov, A.S., Knirel, Y.A.
Structures and serospecificity of threoninecontaining O polysaccharides of two clinical isolates belonging to the genus proteus and their classification into O11 subserogroups
(2016) Journal of Medical Microbiology, 65 (11), pp. 1260-1266. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84995947179&doi=10.1099%2fjmm.0.000360&partnerID=40&md5=f0df7058f93839a58d6e3652d6343fd1

DOI: 10.1099/jmm.0.000360

Gazieva, G.A., Anikina, L.V., Pukhov, S.A., Karpova, T.B., Nelyubina, Y.V., Kravchenko, A.N.
Substituted N-aminothioglycolurils containing thiosemicarbazone moiety and their cytotoxic activity in vitro
(2016) Molecular Diversity, 20 (4), pp. 837-846. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969833453&doi=10.1007%2fs11030-016-9671-1&partnerID=40&md5=154520a1b47de5bd9231a97b13c9807c

DOI: 10.1007/s11030-016-9671-1

Terent'ev, A.O., Mulina, O.M., Pirgach, D.A., Syroeshkin, M.A., Glinushkin, A.P., Nikishin, G.I.
Electrochemical synthesis of sulfonamides from arenesulfonohydrazides or sodium p-methylbenzenesulfinate and amines
(2016) Mendeleev Communications, 26 (6), pp. 538-539. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84997426737&doi=10.1016%2fj.mencom.2016.11.027&partnerID=40&md5=3775c808deb429c6c1c6a10390c7c0fd

DOI: 10.1016/j.mencom.2016.11.027

Semionova, V.V., Korolev, V.V., Glebov, E.M., Shirinyan, V.Z., Sapchenko, S.A.
Photochromic properties of polycrystals: 2,3-diarylcyclopentenone and its adduct with a metal-organic coordination polymer
(2016) Journal of Structural Chemistry, 57 (6), pp. 1216-1224. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010651064&doi=10.1134%2fS0022476616060238&partnerID=40&md5=a68322d820bccf79b05f1c50fa671261

DOI: 10.1134/S0022476616060238

Churusova, S.G., Aleksanyan, D.V., Vasil'ev, A.A., Nelyubina, Y.V., Novikov, V.V., Pavlov, A.A., Denisov, G.L., Klemenkova, Z.S., Kozlov, V.A.
5,6- and 6,6-Membered Palladium(II) Pincer Complexes Based on Functionalized Carboxamides with Ancillary Sulfur and Nitrogen Donors
(2016) European Journal of Inorganic Chemistry, 2016 (33), pp. 5271-5280. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84995685607&doi=10.1002%2fejic.201601093&partnerID=40&md5=86e9a549f7e97f64e95ab29db6c1c1e5

DOI: 10.1002/ejic.201601093

Markov, P.V., Bragina, G.O., Rassolov, A.V., Mashkovsky, I.S., Baeva, G.N., Tkachenko, O.P., Yakushev, I.A., Vargaftik, M.N., Stakheev, A.Y.
Performance of a bimetallic Pd–In catalyst in the selective liquid-phase hydrogenation of internal and terminal alkynes
(2016) Mendeleev Communications, 26 (6), pp. 494-496. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996957470&doi=10.1016%2fj.mencom.2016.11.011&partnerID=40&md5=860f9f1688361b023cf8ff2f0a12e481

DOI: 10.1016/j.mencom.2016.11.011

Krylov, V.B., Argunov, D.A., Nifantiev, N.E.
Pyranoside-into-furanoside rearrangement of D-glucuronopyranoside derivatives
(2016) Mendeleev Communications, 26 (6), pp. 483-484. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84997218102&doi=10.1016%2fj.mencom.2016.11.007&partnerID=40&md5=6f847064f793f0d91012af6d874213c8

DOI: 10.1016/j.mencom.2016.11.007

Izmest'ev, A.N., Gazieva, G.A., Sigay, N.V., Serkov, S.A., Karnoukhova, V.A., Kachala, V.V., Shashkov, A.S., Zanin, I.E., Kravchenko, A.N., Makhova, N.N.
An effective one-pot access to polynuclear dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties via a 1,3-dipolar cycloaddition strategy
(2016) Beilstein Journal of Organic Chemistry, 12, pp. 2240-2249. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994417383&doi=10.3762%2fbjoc.12.216&partnerID=40&md5=b7344b9f6b19a0de3a7461e304012fa7

DOI: 10.3762/bjoc.12.216

Vereshchagin, A.N., Elinson, M.N., Korshunov, A.D., Anisina, Y.E., Novikov, R.A., Goloveshkin, A.S., Bushmarinov, I.S., Zlotin, S.G., Egorov, M.P.
Stereoselective Michael Halogenation Initiated Ring Closure (MHIRC) Synthesis of Spirocyclopropanes from Benzylidenemalononitriles and 3-Arylisoxazol-5(4H)-ones
(2016) Synlett, 27 (17), pp. 2489-2493. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979202555&doi=10.1055%2fs-0035-1562690&partnerID=40&md5=b1ac4b8fe4673f062a0885f3476caa5f

DOI: 10.1055/s-0035-1562690

Ogurtsov, V.A., Shastin, A.V., Zlotin, S.G., Rakitin, O.A.
Erratum: Corrigendum to “Short and efficient synthesis of 1-(2-oxido-1,2,5-oxadiazol-3-yl)alkyl nitrates by unconventional nitrooxylation of 3-alkyl-1,2,5-oxadiazole 2-oxides” (Tetrahedron Lett. (2016) 57(36) (4027–4030))
(2016) Tetrahedron Letters, 57 (42), p. 4770. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988599194&doi=10.1016%2fj.tetlet.2016.09.019&partnerID=40&md5=b45217b4bdf474080eadabe456f3ebff

DOI: 10.1016/j.tetlet.2016.09.019

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
(2016) Synthesis (Germany), . Article in Press. 
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

Sukhorukov, A.Y., Sukhanova, A.A., Zlotin, S.G.
Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients
(2016) Tetrahedron, 72 (41), pp. 6191-6281. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987949040&doi=10.1016%2fj.tet.2016.07.067&partnerID=40&md5=f8bb65807e7d04a5e4a5d97c91cb0688

DOI: 10.1016/j.tet.2016.07.067

Kuznetsov, N.Y., Tikhov, R.M., Strelkova, T.V., Bubnov, Y.N., Lyssenko, K.A.
Synthesis of 6-amino-2,3-dihydropyridine-4-thiones via novel efficient thioenolate-carbodiimide rearrangement
(2016) Tetrahedron Letters, 57 (41), pp. 4525-4528. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987962182&doi=10.1016%2fj.tetlet.2016.08.010&partnerID=40&md5=6a5fe725b7a28906ed81c6699e7b7520

DOI: 10.1016/j.tetlet.2016.08.010

Fedorov, O.V., Struchkova, M.I., Dilman, A.D.
Silicon Reagent with Functionalized Tetrafluoroethylene Fragments: Preparation and Coupling with Aldehydes
(2016) Journal of Organic Chemistry, 81 (19), pp. 9455-9460. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84990882856&doi=10.1021%2facs.joc.6b01739&partnerID=40&md5=4f9890251eef13aa5f97400cfed06f62

DOI: 10.1021/acs.joc.6b01739

Asquith, C.R.M., Konstantinova, L.S., Laitinen, T., Meli, M.L., Poso, A., Rakitin, O.A., Hofmann-Lehmann, R., Hilton, S.T.
Evaluation of Substituted 1,2,3-Dithiazoles as Inhibitors of the Feline Immunodeficiency Virus (FIV) Nucleocapsid Protein via a Proposed Zinc Ejection Mechanism
(2016) ChemMedChem, pp. 2119-2126. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989810189&doi=10.1002%2fcmdc.201600260&partnerID=40&md5=6556b853f4434939bd5b5c50808234e1

DOI: 10.1002/cmdc.201600260

Ramkumar, K., Samanta, S., Kyani, A., Yang, S., Tamura, S., Ziemke, E., Stuckey, J.A., Li, S., Chinnaswamy, K., Otake, H., Debnath, B., Yarovenko, V., Sebolt-Leopold, J.S., Ljungman, M., Neamati, N.
Mechanistic evaluation and transcriptional signature of a glutathione S-transferase omega 1 inhibitor
(2016) Nature Communications, 7, art. no. 13084, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84990986159&doi=10.1038%2fncomms13084&partnerID=40&md5=ea74f0d8a3aa75fbd475bf533801b0e9

DOI: 10.1038/ncomms13084

Zdorovenko, E.L., Kadykova, A.A., Varbanets, L.D., Shashkov, A.S., Kiprianova, E.A., Brovarskaya, O.S., Knirel, Y.A.
Structure of the O-specific polysaccharides of Pseudomonas chlororaphis subsp. chlororaphis UCM B-106
(2016) Carbohydrate Research, 433, pp. 1-4. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978219417&doi=10.1016%2fj.carres.2016.06.013&partnerID=40&md5=f3ee059f259bca61e1be4328be16e3d6

DOI: 10.1016/j.carres.2016.06.013

Scherbakov, A.M., Levina, I.S., Kulikova, L.E., Fedyushkina, I.V., Skvortsov, V.S., Veselovsky, A.V., Kuznetsov, Y.V., Zavarzin, I.V.
Cytotoxic activity and molecular modeling of progestins, pregna-D′-pentaranes
(2016) Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 10 (4), pp. 341-345. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996520760&doi=10.1134%2fS1990750816040077&partnerID=40&md5=4291597ab84dc3a5c8b3aef96a22ce98

DOI: 10.1134/S1990750816040077

Dalinger, I.L., Suponitsky, K.Y., Pivkina, A.N., Sheremetev, A.B.
Novel Melt-Castable Energetic Pyrazole: A Pyrazolyl-Furazan Framework Bearing Five Nitro Groups
(2016) Propellants, Explosives, Pyrotechnics, 41 (5), pp. 789-792. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991406680&doi=10.1002%2fprep.201600050&partnerID=40&md5=81e9f428c1a8980f0218cf10b00a0291

DOI: 10.1002/prep.201600050

Nikitushkin, V.D., Shleeva, M.O., Zinin, A.I., Trutneva, K.A., Ostrovsky, D.N., Kaprelyants, A.S.
The main pigment of the dormant Mycobacterium smegmatis is porphyrin
(2016) FEMS Microbiology Letters, 363 (19), art. no. fnw206, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84992206943&doi=10.1093%2ffemsle%2ffnw206&partnerID=40&md5=ab98c53f6615f35e8f484600fc95eaf5

DOI: 10.1093/femsle/fnw206

Feduschak, T., Akimov, A., Morozov, M., Uymin, M., Zaikovskii, V., Prosvirin, I., Vosmerikov, A., Zhuravkov, S., Vlasov, V., Kogan, V.
Synthesis and characterization of mechanically activated bulky molybdenum sulphide catalysts [Synthèse et caractérisation de catalyseurs massifs à base de disulfure de molybdène par activation mécanique]
(2016) Comptes Rendus Chimie, 19 (10), pp. 1315-1325. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959576331&doi=10.1016%2fj.crci.2016.01.011&partnerID=40&md5=9e224e43567ad963c5cce1427d1e7bf8

DOI: 10.1016/j.crci.2016.01.011

Dorokhov, V.S., Kamorin, M.A., Rozhdestvenskaya, N.N., Kogan, V.M.
Synthesis and conversion of alcohols over modified transition metal sulphides
(2016) Comptes Rendus Chimie, 19 (10), pp. 1184-1193. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84959919633&doi=10.1016%2fj.crci.2015.11.018&partnerID=40&md5=37ca165a9f551c4b835a01372cdab2a1

DOI: 10.1016/j.crci.2015.11.018

Kalenchuk, A.N., Bogorodskii, S.E., Bogdan, V.I.
Kinetic and thermodynamic parameters of hydrogen release during the heterogeneous catalytic dehydrogenation of cis- and trans-isomers of perhydro-m-terphenyl
(2016) Russian Journal of Physical Chemistry A, 90 (10), pp. 1921-1924. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987915626&doi=10.1134%2fS0036024416100162&partnerID=40&md5=cf416c5a0aee9b4aef372e64ee16f995

DOI: 10.1134/S0036024416100162

Isaev, A.N.
O–H···C hydrogen bond in the methane–water complex
(2016) Russian Journal of Physical Chemistry A, 90 (10), pp. 1978-1985. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987923227&doi=10.1134%2fS0036024416100150&partnerID=40&md5=0426ac0864f9fdc23d97d4b01b593bdc

DOI: 10.1134/S0036024416100150

Serykh, A.I.
Low-Dimensional Indium Oxo-Species on the Surface of In<inf>2</inf>O<inf>3</inf>/Al<inf>2</inf>O<inf>3</inf> Catalytic Material: The Sites of Dissociative Adsorption of Hydrogen
(2016) Journal of Physical Chemistry C, 120 (38), pp. 21436-21440. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989306793&doi=10.1021%2facs.jpcc.6b05681&partnerID=40&md5=4bbe467a48942e08ced58e90516a973c

DOI: 10.1021/acs.jpcc.6b05681

Kosheleva, Y.A., Medvedeva, S.M., Shikhaliev, K.S., Zubkov, F.I., Ryzhkova, E.A., Prezent, M.A.
Synthesis of substituted pyrazolo[3,4-d]pyrimidines by reactions of 5-amino-1-phenyl-1H-pyrazole derivatives with N-substituted isatins
(2016) Chemistry of Heterocyclic Compounds, pp. 1-5. Article in Press. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988937097&doi=10.1007%2fs10593-016-1935-2&partnerID=40&md5=6d740e7004087c24ccf8dea85e9cac4c

DOI: 10.1007/s10593-016-1935-2

Borisov, D.D., Novikov, R.A., Tomilov, Y.V.
GaCl<inf>3</inf>-Mediated Reactions of Donor–Acceptor Cyclopropanes with Aromatic Aldehydes
(2016) Angewandte Chemie — International Edition, 55 (40), pp. 12233-12237. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84990219134&doi=10.1002%2fanie.201603927&partnerID=40&md5=1a555bbe7553b942f88a0d5110ea6a52

DOI: 10.1002/anie.201603927

Egorova, K.S., Ananikov, V.P.
Which Metals are Green for Catalysis? Comparison of the Toxicities of Ni, Cu, Fe, Pd, Pt, Rh, and Au Salts
(2016) Angewandte Chemie — International Edition, 55 (40), pp. 12150-12162. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84990177883&doi=10.1002%2fanie.201603777&partnerID=40&md5=8d5e6af36efb3bab9dc097da80bc65db

DOI: 10.1002/anie.201603777

Platonov, D.N., Okonnishnikova, G.P., Salikov, R.F., Tomilov, Y.V.
Synthesis and UV–vis spectra of a new type of dye via a decarboxylative azo coupling reaction
(2016) Tetrahedron Letters, 57 (38), pp. 4311-4313. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84984680108&doi=10.1016%2fj.tetlet.2016.08.043&partnerID=40&md5=6933a4ce4378327ae7f5eafbf025f3ad

DOI: 10.1016/j.tetlet.2016.08.043

Fershtat, L.L., Larin, A.A., Epishina, M.A., Kulikov, A.S., Ovchinnikov, I.V., Ananyev, I.V., Makhova, N.N.
Regioselective synthesis of bifuroxanyl systems with the 3-nitrobifuroxanyl core via a one-pot acylation/nitrosation/cyclization cascade
(2016) Tetrahedron Letters, 57 (38), pp. 4268-4272. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84984783390&doi=10.1016%2fj.tetlet.2016.08.011&partnerID=40&md5=c2766a1af0a41664397e84e914a33df4

DOI: 10.1016/j.tetlet.2016.08.011

Kashparova, V.P., Klushin, V.A., Leontyeva, D.V., Smirnova, N.V., Chernyshev, V.M., Ananikov, V.P.
Selective Synthesis of 2,5-Diformylfuran by Sustainable 4-acetamido-TEMPO/Halogen-Mediated Electrooxidation of 5-Hydroxymethylfurfural
(2016) Chemistry — An Asian Journal, 11 (18), pp. 2578-2585. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988372940&doi=10.1002%2fasia.201600801&partnerID=40&md5=9261180dd289bf7a5a3d87b3442f3ee0

DOI: 10.1002/asia.201600801

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
(2016) Synthesis (Germany), . Article in Press. 
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

Eliseev, O.L., Tsapkina, M.V., Lapidus, A.L.
Fischer–Tropsch synthesis on cobalt catalysts with alkaline earth metal additives
(2016) Solid Fuel Chemistry, 50 (5), pp. 282-285. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991799949&doi=10.3103%2fS0361521916050050&partnerID=40&md5=e244c10e467431a7e4ed15db542c4c9f

DOI: 10.3103/S0361521916050050

Kokorekin, V.A., Yaubasarova, R.R., Neverov, S.V., Petrosyan, V.A.
Reactivity of electrogenerated thiocyanogen in the thiocyanation of pyrazolo[1,5-a]pyrimidines
(2016) Mendeleev Communications, 26 (5), pp. 413-414. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989204401&doi=10.1016%2fj.mencom.2016.09.016&partnerID=40&md5=a9dcbcaad68e0db7c6498ac8041ff346

DOI: 10.1016/j.mencom.2016.09.016

Elinson, M.N., Ryzhkov, F.V., Vereshchagin, A.N., Zaimovskaya, T.A., Korolev, V.A., Egorov, M.P.
Multicomponent assembling of isatins, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-ones: one-pot efficient approach to privileged spiro[indoline-3,4’-pyrano[3,2-c]pyridine]-2,5’(6’H)-dione scaffold
(2016) Mendeleev Communications, 26 (5), pp. 399-401. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989171920&doi=10.1016%2fj.mencom.2016.09.011&partnerID=40&md5=2796547f06179ec6b0c19cbfe163a325

DOI: 10.1016/j.mencom.2016.09.011

Kucherenko, A.S., Perepelkin, V.V., Zhdankina, G.M., Kryshtal, G.V., Srinivasan, E., Inani, H., Zlotin, S.G.
Ionic liquid supported 4-HO-Pro-Val derived organocatalysts for asymmetric aldol reactions in the presence of water
(2016) Mendeleev Communications, 26 (5), pp. 388-390. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989189604&doi=10.1016%2fj.mencom.2016.09.007&partnerID=40&md5=919d7b08b823f424b15808c265f2caa3

DOI: 10.1016/j.mencom.2016.09.007

Paulovičová, E., Paulovičová, L., Pilišiová, R., Jančinová, V., Yashunsky, D.V., Karelin, A.A., Tsvetkov, Y.E., Nifantiev, N.E.
The evaluation of β-(1 → 3)-nonaglucoside as an anti-Candida albicans immune response inducer
(2016) Cellular Microbiology, 18 (9), pp. 1294-1307. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84982163209&doi=10.1111%2fcmi.12631&partnerID=40&md5=03d3bd50c0fc10c8bfe63cbc5a5e08e0

DOI: 10.1111/cmi.12631

Usachev, N.Y., Gerzeliev, I.M., Kharlamov, V.V., Kalinin, V.P., Belanova, E.P., Kanaev, S.A., Kazakov, A.V., Starostina, T.S.
Oxidative conversion of ethane involving lattice oxygen of molybdenum systems modified with aluminum, gallium, or yttrium oxide
(2016) Petroleum Chemistry, 56 (9), pp. 841-845. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010015593&doi=10.1134%2fS0965544116090218&partnerID=40&md5=84c6fe3141343fe863e0aae1ac14e4bb

DOI: 10.1134/S0965544116090218

Nirvanappa, A.C., Mohan, C.D., Rangappa, S., Ananda, H., Sukhorukov, A.Y., Shanmugam, M.K., Sundaram, M.S., Nayaka, S.C., Girish, K.S., Chinnathambi, A., Zayed, M.E., Alharbi, S.A., Sethi, G., Basappa, Rangappa, K.S.
Novel synthetic oxazines target NF-κB in colon cancer in vitro and inflammatory bowel disease in vivo
(2016) PLoS ONE, 11 (9), art. no. e0163209, . 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991691519&doi=10.1371%2fjournal.pone.0163209&partnerID=40&md5=6f00016b5dae76465ec0667c65e81ce9

DOI: 10.1371/journal.pone.0163209

Bastrakov, M.A., Geraseva, A.O., Starosotnikov, A.M., Fedyanin, I.V., Pavlov, A.A., Ugrak, B.I., Shevelev, S.A.
Synthesis of nitro pyrido- and dipyrido[1,4]oxazines
(2016) Mendeleev Communications, 26 (5), pp. 383-385. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989182949&doi=10.1016%2fj.mencom.2016.09.005&partnerID=40&md5=bdb119191519ca8fae41ba1a359da5d8

DOI: 10.1016/j.mencom.2016.09.005

Markov, P.V., Bragina, G.O., Baeva, G.N., Tkachenko, O.P., Mashkovskii, I.S., Yakushev, I.A., Vargaftik, M.N., Stakheev, A.Y.
Supported catalysts based on Pd–In nanoparticles for the liquid-phase hydrogenation of terminal and internal alkynes: 1. formation and structure
(2016) Kinetics and Catalysis, 57 (5), pp. 617-624. Cited 4 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991055971&doi=10.1134%2fS002315841605013X&partnerID=40&md5=d514ab004547795d9610d65c6041c277

DOI: 10.1134/S002315841605013X

Minyaev, M.E., Vinogradov, A.A., Roitershtein, D.M., Borisov, R.S., Ananyev, I.V., Churakov, A.V., Nifant'Ev, I.E.
Catalytic activity of phenyl substituted cyclopentadienyl neodymium complexes in the ethylene oligomerization process
(2016) Journal of Organometallic Chemistry, 818, pp. 128-136. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84973861964&doi=10.1016%2fj.jorganchem.2016.06.003&partnerID=40&md5=827f23891612e801d0e8a28a40341811

DOI: 10.1016/j.jorganchem.2016.06.003

Kuznetsov, V.V., Shevtsov, A.V., Pleshchev, M.I., Strelenko, Y.A., Makhova, N.N.
Diastereoselective synthesis of 1,3-di- and 1,3,3-trisubstituted diaziridines coupled with neurotransmitter amino acids
(2016) Mendeleev Communications, 26 (5), pp. 391-394. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989189617&doi=10.1016%2fj.mencom.2016.09.008&partnerID=40&md5=ba8361dfa21707ccf9eb90e26854e9ea

DOI: 10.1016/j.mencom.2016.09.008

Kuzmin, V.A., Podrugina, T.A., Nekipelova, T.D., Doroshenko, I.A., Proskurnina, M.V., Golovina, G.V., Radchenko, E.V., Kostyukov, A.A., Temnov, V.V., Matveeva, E.D., Palyulin, V.A., Zefirov, N.S.
New phosphonate-substituted tricarbocyanines and their interaction with bovine serum albumin
(2016) Doklady Chemistry, 470 (1), pp. 264-267. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989339590&doi=10.1134%2fS001250081609007X&partnerID=40&md5=8d4242ad7cbd5637a6b76bf5200fc16e

DOI: 10.1134/S001250081609007X

Finashina, E.D., Kustov, L.M., Krasovskii, V.G., Formenova, E.I.
Carboxylation of 2-methylbutyn-3-ol-2 on Ag- and Cu-containing catalysts
(2016) Russian Journal of Physical Chemistry A, 90 (9), pp. 1729-1732. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84982203489&doi=10.1134%2fS0036024416090089&partnerID=40&md5=0dba722a2f035eab6924eff777d9d457

DOI: 10.1134/S0036024416090089

Usachev, N.Y., Gerzeliev, I.M., Belanova, E.P., Kazakov, A.V., Kalinin, V.P., Kharlamov, V.V., Kanaev, S.A., Starostina, T.S.
Thermal and structural properties of molybdenum systems modified with aluminum, gallium, or yttrium oxide
(2016) Petroleum Chemistry, 56 (9), pp. 846-851. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009968793&doi=10.1134%2fS096554411609022X&partnerID=40&md5=46c5b59c7b43681eff8b0cd868d8369c

DOI: 10.1134/S096554411609022X

Vedenyapina, M.D., Strel’tsova, E.D., Vil’, V.A., Terent’ev, A.O., Vedenyapin, A.A.
Adsorption of benzoyl peroxide on activated carbon
(2016) Solid Fuel Chemistry, 50 (5), pp. 306-309. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991755566&doi=10.3103%2fS0361521916050086&partnerID=40&md5=7d073576f5e8b1bd910e11650fc31e7a

DOI: 10.3103/S0361521916050086

Markov, P.V., Bragina, G.O., Baeva, G.N., Mashkovskii, I.S., Rassolov, A.V., Yakushev, I.A., Vargaftik, M.N., Stakheev, A.Y.
Supported catalysts based on Pd–In nanoparticles for the liquid- phase hydrogenation of terminal and internal alkynes: 2. catalytic properties
(2016) Kinetics and Catalysis, 57 (5), pp. 625-631. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991045320&doi=10.1134%2fS0023158416050141&partnerID=40&md5=83b642f2edaecf038e120b4b9aaffd60

DOI: 10.1134/S0023158416050141

Streshinskaya, G.M., Sashkov, A.S., Tul’skaya, E.M., Senchenkova, S.N., Dmitrenok, A.S., Piskunkova, N.F., Bueva, O.V., Evtushenko, L.I.
Cell wall glycopolymers of type strains from three species of the genus Actinoplanes
(2016) Biochemistry (Moscow), 81 (9), pp. 999-1012. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987971451&doi=10.1134%2fS0006297916090091&partnerID=40&md5=f5e2261d9366a788b49bdce50cf1465d

DOI: 10.1134/S0006297916090091

Ananikov, V.P., Galkin, K.I., Egorov, M.P., Sakharov, A.M., Zlotin, S.G., Redina, E.A., Isaeva, V.I., Kustov, L.M., Gening, M.L., Nifantiev, N.E.
Challenges in the development of organic and hybrid molecular systems
(2016) Mendeleev Communications, 26 (5), pp. 365-374. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988917248&doi=10.1016%2fj.mencom.2016.09.001&partnerID=40&md5=fe7c68ae287fdd5323b96aaf7bee7d52

DOI: 10.1016/j.mencom.2016.09.001

Krasnobaeva, O.N., Belomestnykh, I.P., Nosova, T.A., Kondakov, D.F., Elizarova, T.A., Danilov, V.P.
Europium oxide containing catalysts for oxidative dehydrogenation of alkanes
(2016) Russian Journal of Inorganic Chemistry, 61 (9), pp. 1074-1079. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84989856985&doi=10.1134%2fS0036023616090126&partnerID=40&md5=1ae3048c01d344685026bea3b0086764

DOI: 10.1134/S0036023616090126

Elinson, M.N., Ryzhkov, F.V., Nasybullin, R.F., Vereshchagin, A.N., Egorov, M.P.
Fast Efficient and General PASE Approach to Medicinally Relevant 4H,5H-Pyrano-[4,3-b]pyran-5-one and 4,6-Dihydro-5H-pyrano-[3,2-c]pyridine-5-one Scaffolds
(2016) Helvetica Chimica Acta, 99 (9), pp. 724-731. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987704776&doi=10.1002%2fhlca.201600150&partnerID=40&md5=39eca4a7777cdeab88a642db623aff28

DOI: 10.1002/hlca.201600150

Gus’kov, P.O., Ryzhov, A.N., Zhagfarov, F.G., Smolenskii, E.A., Lapidus, A.L.
Mathematical simulation of the kinetics of visbreaking of tars
(2016) Solid Fuel Chemistry, 50 (5), pp. 286-299. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991746859&doi=10.3103%2fS0361521916050062&partnerID=40&md5=5a67a082130729678774237a14636ee6

DOI: 10.3103/S0361521916050062

Vedenyapina, M.D., Kuznetsov, V.V., Makhova, N.N., Vedenyapin, A.A.
Mechanism of the anodic dissolution of gold in solutions of 6-alkyl-1,5-diazabicyclo[3.1.0]hexanes
(2016) Russian Journal of Physical Chemistry A, 90 (9), pp. 1903-1908. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84982199296&doi=10.1134%2fS0036024416090284&partnerID=40&md5=716ba9af2f274e74a6d1cffb05d178a3

DOI: 10.1134/S0036024416090284

Wittmann, A., Lamprinaki, D., Bowles, K.M., Katzenellenbogen, E., Knirel, Y.A., Whitfield, C., Nishimura, T., Matsumoto, N., Yamamoto, K., Iwakura, Y., Saijo, S., Kawasaki, N.
Dectin-2 recognizes mannosylated O-antigens of human opportunistic pathogens and augments lipopolysaccharide activation of myeloid cells
(2016) Journal of Biological Chemistry, 291 (34), pp. 17629-17638. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84984683744&doi=10.1074%2fjbc.M116.741256&partnerID=40&md5=e46656df9115a028bdfd5cfb5eb28170

DOI: 10.1074/jbc.M116.741256

Isaev, A.N.
Intermolecular charge transfer as evidence for unusual O-H...C(sp3) hydrogen bond
(2016) Computational and Theoretical Chemistry, 1090, pp. 180-192. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84975727034&doi=10.1016%2fj.comptc.2016.06.014&partnerID=40&md5=68c0de05f1bf561e3e38f934319d7860

DOI: 10.1016/j.comptc.2016.06.014

Podvalnyy, N.M., Chizhov, A.O., Zinin, A.I., Kononov, L.O.
Rapid synthesis of linear homologous oligoarabinofuranosides related to mycobacterial lipoarabinomannan and a neoglycoconjugate thereof
(2016) Carbohydrate Research, 431, pp. 25-32. Cited 1 time.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84971641012&doi=10.1016%2fj.carres.2016.05.009&partnerID=40&md5=6c1646a51e7afefaea4b793e54b01cf9

DOI: 10.1016/j.carres.2016.05.009

Yaremenko, I.A., Vil', V.A., Demchuk, D.V., Terent'ev, A.O.
Rearrangements of organic peroxides and related processes
(2016) Beilstein Journal of Organic Chemistry, 12, pp. 1647-1748. Cited 2 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988700540&doi=10.3762%2fbjoc.12.162&partnerID=40&md5=fa9929720e9ba26d120c3ae00f9b0741

DOI: 10.3762/bjoc.12.162

Nikulshin, P.A., Salnikov, V.A., Varakin, A.N., Kogan, V.M.
The use of CoMoS catalysts supported on carbon-coated alumina for hydrodeoxygenation of guaiacol and oleic acid
(2016) Catalysis Today, 271, pp. 45-55. Cited 3 times.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84938795198&doi=10.1016%2fj.cattod.2015.07.032&partnerID=40&md5=67b20cb543c833a7f28896ad332b3a4b

DOI: 10.1016/j.cattod.2015.07.032

Novakov, I.A., Yablokov, A.S., Orlinson, B.S., Navrotskii, M.B., Kirillov, I.A., Vernigora, A.A., Babushkin, A.S., Kachala, V.V., Schols, D.
Synthesis and antiviral properties of new derivatives of 2-(alkylsulfanyl)-6-[1-(2,6-difluorophenyl)cyclopropyl]-5-methylpyrimidin-4(3H)-one
(2016) Russian Journal of Organic Chemistry, 52 (8), pp. 1188-1193. 
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84988859673&doi=10.1134%2fS1070428016080169&partnerID=40&md5=c42d9c372b0f04b9b2a6d4a0072984e3

DOI: 10.1134/S1070428016080169