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Авторы, Название Выходные данные
1 T.B. Anisimova, N.A. Bokach, F.M. Dolgushin, V.Yu. Kukushkin“Dialkylcyanamides are more reactive substrates toward metal-mediated nucleophilic addition than alkylcyanides” Dalton Trans., 2013, 42, 12460-12467
DOI: 10.1039/c3dt51137e
2 M.A. Kinzhalov, K.V. Luzyanin, V.P. Boyarskiy, M. Haukka, V.Yu. Kukushkin“ADC-Based palladium catalysts for aqueous Suzuki–Miyaura cross-coupling exhibit greater activity than the most advantageous catalytic systems” Organometallics, 2013, 32, 5212-5223
DOI: 10.1021/om4007592
3 I.O. Koshevoy, A.J. Karttunen, I.S. Kritchenkou, D.V. Krupenya, S.I. Selivanov, A.S. Melnikov, S.P. Tunik, M. Haukka, T.A. Pakkanen“Sky-Blue Luminescent Au–I–Ag–I Alkynyl-Phosphine Clusters” Inorg. Chem., 2013, 52, 3663-3673
DOI: 10.1021/ic302105a
4 P.V. Gushchin, M.L. Kuznetsov, M. Haukka, V.Yu. Kukushkin“Recognition of a novel type X=N−Hal…Hal’ (X = С, S, P; Hal = F, Cl, Br, I) halogen bonding” J. Phys. Chem. A, 2013, 117, 2827-2834
DOI: 10.1021/jp3112149
5 S. Miltsov, V. Karavan,V. Boyarsky, S. Gómez-de Pedro, J. Alonso-Chamarro, M. Puyol“New acyclic Pd–diaminocarbene catalyst for Suzuki arylation of meso-chlorosubstituted tricarboindocyanine dyes” Tetrahedron Letters, 2013, 54, 1202-1204
DOI: 10.1016/j.tetlet.2012.12.060
6 E.A. Savicheva, V.P. Boyarskiy“Palladium catalyzed cyanation of o-dichloroarenes with potassium hexacyanoferrate(ii)” Russ. Chem. Bull. 2013, 61(3), 980-983
DOI: 10.1007/s11172-012-0141-3.
7 D.V. Kurandiva, E.V. Eliseenkov, A.A. Petrov, V.P. Boyarskii“N(2)-Monosubstituted bishydrazides of oxalic acid as new efficient components of the system for the copper-catalyzed C-N cross-coupling in water” Russ. Chem. Bull., 2013, 61(3), 1009-1013
DOI: 10.1007/s11172-012-0130-6
8 S.N. Morozkina, Sh.N. Abusalimov, S.I. Selivanov, A.G. Shavva“Synthesis and biological activity of some 8 alpha-analogs of steroidal estrogens” Russ. J. Org. Chem., 2013, 49(4), 603-609
DOI: 10.1134/S1070428013040180
9 T.Sh. Khaibulova, I.A. Boyarskaya, V.P. Boyarskii“Steric effect of substituents in haloarenes on the rate of cross-coupling reactions” Russ. J. Org. Chem., 2013, 49(3), 360-365
DOI: 10.1134/S1070428013030081
10 A.A. Petrov, A.N. Kasatochkin“Synthesis of 6,7,8,9-Tetrahydropyrazolo[1,5-a]quinazolines containing a 5-phenylamine fragment” Russ. J. Org. Chem., 2013, 49(8), 1250-1252
DOI: 10.1134/S1070428013080307
11 A.A. Petrov, A.N. Kasatochkin“Synthesis of 8,9-dihydro[1,2,4]triazolo[1,5-a]-quinazolin-6(7H)-one derivatives” Russ. J. Org. Chem., 2013, 49(4), 502-507
DOI: 10.1134/S1070428013040027
12 V.N. Mikhailov, E.A. Savicheva, V.N. Sorokoumov, V.P. Boyarskii“Catalytic activity of palladium(II) diaminocarbene complexes in the Sonogashira and Suzuki reactions” Russ. J. Org. Chem., 2013, 49(4), 551-554
DOI: 10.1134/S107042801304009X
13 D.S. Ryabukhin, V.N. Sorokoumov, E.A. Savicheva, V.P. Boyarskiy, I.A. Balova, A.V. Vasilyev“Catalytic activity of palladium acyclic diaminocarbene complexes in the synthesis of 1,3-diarylpropynones via Sonogashira reaction: cross- versus homo-coupling” Tetrahedron Letters, 2013, 54, 2369-2372
DOI: 10.1016/j.tetlet.2013.02.086
14 A.L. Mindich, N.A. Bokach, M.L. Kuznetsov, M. Haukka, A.P. Zhdanov, K.Yu. Zhizhin, S.A. Miltsov, N.T. Kuznetsov, V.Yu. Kukushkin“Coupling of Azomethine Ylides with Nitrilium Derivatives of closo-Decaborate Clusters: A Synthetic and Theoretical Study” ChemPlusChem, 2012, 77(12), 1075-1086
DOI: 10.1002/cplu.201200257
15 A.G. Tskhvorebov, K.V. Luzyanin, M. Haukka, V. Yu. Kukushkin“Synthesis and Characterization of cis-(RNC)(2)Pt-II Species Useful as Synthons for Generation of Various (Aminocarbene)Pt-II Complexes” J. Chem. Cryst., 2012, 42(12), 1170-1175
DOI: 10.1007/s10870-012-0371-0
16 A.S. Kritchenkov, N.A. Bokach, G.L. Starova, V. Yu. Kukushkin“A Palladium(II) Center Activates Nitrile Ligands toward 1,3-Dipolar Cycloaddition of Nitrones Substantially More than the Corresponding Platinum(II) Center” Inorg. Chem., 2012, 51(21), 11971-11979
DOI: 10.1021/ic301866y
17 B.G.M. Rocha, R. Wanke, M.F.C. Guedes da Silva, K.V. Luzyanin, L.M.D.R.S. Martins, P.Smolénski, A.J.L. Pombeiro“Reactivity of bulky tris(phenylpyrazolyl)methanesulfonate copper(I) complexes towards small unsaturated molecules” J. Organomet. Chem., 2012, 714, 47-52
DOI: 10.1016/j.jorganchem.2012.03.022
18 S.N. Morozkina, S.K. Nikol’skaya, A.S. Chentsova, A.S. Drozdov, G.L. Starova, S.I. Selivanov, A.G. Shavva“Ionic hydrogenation of estra-1,3,5(10),8,14-pentaenes” Russ. J. Org. Chem., 2012, 48(9), 1245-1251
DOI: 10.1134/S1070428012090175
19 A.N. Chernyshev, N.A. Bokach, P.V. Gushchin, M. Haukka, V.Yu. Kukushkin“Reactions of platinum(IV)-bound nitriles with isomeric nitroanilines: addition vs. substitution” Dalton Trans., 2012, 41(41), 12857-12864
DOI: 10.1039/c2dt30986f
20 J.R. Shakirova, E.V. Grachova, A.A. Melekhova, D.V. Krupenya, V.V. Gurzhiy, A.J. Karttunen, I.O. Koshevoy, A.S. Melnikov, S.P. Tunik“Luminescent AuI-CuI Triphosphane Clusters That Contain Extended Linear Arylacetylenes” Eur. J. Inorg. Chem., 2012, 25, 4048-4056
DOI: 10.1002/ejic.201200362
21 T.M. Dau, J.R. Shakirova, A. Doménech, J. Jänis, M. Haukka, E.V. Grachova, I.O. Koshevoy“Ferrocenyl-functionalized tetranuclear gold(I) and gold(I)-copper(I) complexes based on tridentate phosphanes” Eur. J. Inorg. Chem. 2013, 28, 4976-4983
DOI: 10.1002/ejic.201300615
22 P.Y. Dereza, I.S. Krytchankou, D.V. Krupenya, V.V. Gurzhiy, I.O. Koshevoy, A.S. Melnikov, S.P. Tunik“Synthesis, structural characterization, and photophysical properties of AuI-CuI heterometallic alkynyl cluster complexes containing N-protected amino acid groups” Z. Anorg. Allg. Chem. 2013, 639(2), 398-402
DOI: 10.1002/zaac.201200481
23 I.O. Koshevoy, A.J. Karttunen, I.S. Kritchenkou, D.V. Krupenya, S.I. Selivanov, A.S. Melnikov, T.A. Pakkanen“Sky-blue luminescent AuI-AgI alkynyl-phosphine clusters” Inorg. Chem. 2013, 52(7), 3663-3673
DOI: 10.1021/ic302105a
24 I.S. Krytchankou, D.V. Krupenya, V.V. Gurzhiy, A.A. Belyaev, A.J. Karttunen, I.O. Koshevoy, S.P. Tunik“Synthesis, characterization and photophysical properties of gold(I)-copper(I) alkynyl clusters with 1,4-bis(diphenylphosphino)butane, effect of the diphosphine ligand on luminescence characteristics” J. Organomet. Chem. 2013, 723, 65-71
DOI: 10.1016/j.jorganchem.2012.09.003
25 E.P. Shestakova, Y.S. Varshavsky, V.N. Khrustalev, S.N. Smirnov“Synthesis and characterization of acetamidine rhodium(III) cationic methyl complex, trans-[rh(acac)(PPh3)2(CH3) {NHC(NH2)CH3}][BPh4], produced by ammination of acetonitrile ligand in trans-[rh(acac)(PPh3)2(CH 3)(CH3CN)][BPh4]” J. Organomet. Chem. 2013, 735, 47-51
DOI: 10.1016/j.jorganchem.2013.03.015
26 T.Q. Tran, R.S. Savinkov, V.V. Diev, G.L. Starova, A.P. Molchanov“An efficient method of synthesis of isoxazolidine-fused β-lactams via base-promoted cyclization-ring opening of carbamoyl-spirocyclopropane isoxazolidines” Tetrahedron 2013, 69(25), 5173-5177
DOI: 10.1016/j.tet.2013.04.054
27 Y.S. Varshavskii, T.G. Cherkasova, M.R. Gal’ding, V.A. Gindin, I.S. Podkorytov, O.V. Sizova, A.B. Nikol’skii“Direct 13C-31P coupling constant of coordinated triphenylphosphine as a characteristic of electron-withdrawing power of the metal center” Russ. J. Org. Chem. 2013, 83(3), 567-569
DOI: 10.1134/S1070363213030274
28 A.E. Kulyashova, V.N. Sorokoumov, V.V. Popik, I.A. Balova“An acetylene zipper-Sonogashira reaction sequence for the efficient synthesis of conjugated arylalkadiynols” Tetrahedron 2013, 54(18), 2235-2238
DOI: 10.1016/j.tetlet.2013.02.066
29 M.A. Kuznetsov, V.V. Voronin“Thermal transformations of alk-1-enyl-N-phthalimidoaziridines” Russ. J. Org. Chem. 2013, 49(1), 83-94
DOI: 10.1134/S1070428013010156
30 A.P. Molchanov, T.Q. Tran, A.V. Stepakov, V.V. Gurzhii, R.R. Kostikov“Methyl (E)-2-(2-phenylcyclopropylidene)acetate: Synthesis, isomerization, and reaction with 1,3-diphenyl-2-benzofuran” Russ. J. Org. Chem. 2013, 49(4), 530-535
DOI: 10.1134/S1070428013040064
31 M.S. Mishina, A.Yu. Ivanov, D.V. Dar’in, P.S. Lobanov“Reaction of 1,2-dihaloarenes with ethyl 2-(imidazolidin-2-ylidene)acetate. A novel method for the synthesis of 2,3-dihydro-1H-imidazo[1,2-a]indoles and their aza analogs” Chem. Heterocycl. Compd. 2013, 49(4) 648-650
DOI: 10.1007/s10593-013-1293-2
32 O.Yu. Bakulina, E.M. Igumnova, D.V. Dar’in, P.S. Lobanov“Reaction of ethyl 3,3-diaminoacrylate with pyrimidine series o-chloro ketones. Synthesis of pyrido[4,3-d]pyrimidines and 6H-1,3,6,7-tetra-azaphenalenes” Chem. Heterocycl. Compd. 2013, 49(3), 466-471
DOI: 10.1007/s10593-013-1269-2
33 A.P. Molchanov, T.Q. Tran“Regio- and stereoselective cycloaddition of C-Carbamoylnitrones to 1-benzylidene-3,3-dichloro-2,2-dimethylcyclopropane” Chem. Heterocycl. Compd. 2013, 49(3), 479-483
DOI: 10.1007/s10593-013-1271-8
34 A.V. Ivanov, G. Mloston, V.A. Nikolaev“Tetrasubstituted oxathioles and olefins obtained by cycloaddition of 2-diazo-1,3-dicarbonyl compounds to aliphatic thiones” Russ. J. Org. Chem. 2013, 49(7), 1080-1082
DOI: 10.1134/S107042801307021X
35 K.V. Zavyalov, M.S. Novikov, A.F. Khlebnikov, D.S. Yufit“Rh2(OAc)4-catalyzed reaction of α-diazocarbonyl compounds with 2-carbonyl-substituted 2H-azirines” Tetrahedron 2013, 69(23), 4546-4551
DOI: 10.1016/j.tet.2013.04.022
36 N.V. Rostovskii, M.S. Novikov, A.F. Khlebnikov, V.A. Khlebnikov, S.M. Korneev“Rh(II)-carbenoid mediated 2H-azirine ring-expansion as a convenient route to non-fused photo- and thermochromic 2H-1,4-oxazines” Tetrahedron 2013, 69(21), 4292-4301
DOI: 10.1016/j.tet.2013.03.106
37 V.V. Pakal’nis, I.V. Zerova, S.I. Yakimovich, V.V. Alekseyev“Reaction of acylpyruvic acid esters with hydrazides” Chem. Heterocycl. Compd. 2013, 49(3), 408-416
DOI: 10.1007/s10593-013-1261-x
38 A.S. Konev, A.F. Khlebnikov, T.G. Nikiforova, A.A. Virtsev, H. Frauendorf“Synthesis and spectroscopic and electrochemical properties of an axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer” J. Org. Chem. 2013, 78(6), 2542-2552
DOI: 10.1021/jo302763a
39 N.A. Danilkina, E.G. Gorbunova, V.N. Sorokoumov, I.A. Balova“Study of cyclyzation of o-(1-Alkynyl)- and o-(1,3-Butadiynyl)aryltriazenes under the action of acids” Russ. J. Org. Chem. 2012, 48(11), 1424-1434
DOI: 10.1134/S1070428012110048
40 A.S. Pankova, P.R. Golubev, I.V. Ananyev, M.A. Kuznetsov“Synthesis of [2-(Trimethylsilyl)ethynyl]pyrazoles Based on Bis(trimethylsilyl)acetylene and Arylacetyl Chlorides” Eur. J. Org. Chem. 2012, 30, 5965-5971
DOI: 10.1002/ejoc.201200807
41 E.E. Pivneva, A.V. Galenko, D.V. Dar’in, P.S. Lobanov“Rearrangement of the adducts of alpha-(aminocarbonyl)-acetamidoximes with acylacetylenes, leading to 2-aminopyrrole derivatives” Chem. Heterocycl. Compd. 2012, 48(6), 875-880
DOI: 10.1007/s10593-012-1069-0
42 A.P. Molchanov, T.Q. Tran“Regioselective cycloaddition of C-aryl- and C-carbamoylnitrones to methyl 2-benzylidenecyclopropanecarboxylate” Russ. J. Org. Chem. 2012, 48(10), 1283-1288
DOI: 10.1134/S1070428012100041
43 A.P. Molchanov, T.Q. Tran“Reduction and hydrolysis of substituted 5-oxa-6-azaspiro[2.4]heptane-1,2-dicarboxylic acid esters” Russ. J. Org. Chem. 2012, 48(10), 1323-1325
DOI: 10.1134/S1070428012100107
44 A.V. Stepakov, M.S. Ledovskaya, V.M. Boitsov, A.P. Molchanov, R.R. Kostikov, V.V. Gurzhiy, G.L. Starova“Synthesis of isoxazolopyrroloisoquinolines by intramolecular cyclizations of 5-(2-arylethyl)-6-hydroxytetrahydro-4H-pyrrolo[3,4-d]isoxazol-4-ones” Tetrahedron Lett. 2012, 53(40), 5414-5417
DOI: 10.1016/j.tetlet.2012.07.114
45 M.S. Novikov, I.A. Smetanin, A.F. Khlebnikov, N.V. Rostovskii, D.S. Yufit”Synthesis of electron-poor 4-halo-2-azabuta-1,3-dienes by Rh(II)-catalyzed diazo ester-azirine coupling. 2-Azabuta-1,3-diene-2,3-dihydroazete valence isomerism” Tetrahedron Lett. 2012, 53(43), 5777-5780
DOI: 10.1016/j.tetlet.2012.08.063
46 N. Danilkina, M. Nieger, S. Selivanov, S. Braese, I. Balova“Electrophilic Cyclization and Ring-Closing Metathesis as Key Steps in the Synthesis of a 12-Membered Cyclic Enediyne” Eur. J. Org. Chem. 2012, 29, 5660-5664
DOI: 10.1002/ejoc.201200881
47 I.I. Eliseev, N.A. Bokach, M. Haukka, I.A. Golenya“cis-Dichlorido(dimethyl sulfoxide-kS)-(N,N,N’,N’-tetramethylguanidine-kN’’)-platinum(II)” Acta Cryst. E 2013, 69, m117-m118
DOI: 10.1107/S160053681300130X

Статьи с упоминанием оборудования РЦ МРМИ, посланные в печать до официального запуска центра