Articles - Sciact

Articles (231)

#	Публикация
81	Ogurtsov V.A. , Shastin A.V. , Zlotin S.G. , Rakitin O.A. 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 Letters. 2016. V.57. N36. P.4027-4030. DOI: 10.1016/j.tetlet.2016.07.048 WOS Scopus OpenAlex
82	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 Journal of Supercritical Fluids. 2016. V.109. P.35-42. DOI: 10.1016/j.supflu.2015.11.004 WOS Scopus OpenAlex
83	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 Journal of Fluorine Chemistry. 2016. V.183. P.23-29. DOI: 10.1016/j.jfluchem.2016.01.005 WOS Scopus OpenAlex
84	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 Synlett. 2016. V.27. N17. P.2489-2493. DOI: 10.1055/s-0035-1562690 WOS Scopus OpenAlex
85	Sukhanova A.A. , Nelyubina Y.V. , Zlotin S.G. Asymmetric synthesis of 3-prenyl-substituted pyrrolidin-2-ones Mendeleev Communications. 2016. V.26. N6. P.471-473. DOI: 10.1016/j.mencom.2016.11.003 WOS Scopus OpenAlex
86	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 Tetrahedron. 2016. V.72. N47. P.7552-7556. DOI: 10.1016/j.tet.2016.10.006 WOS Scopus OpenAlex
87	Ogurtsov V.A. , Shastin A.V. , Zlotin S.G. , Rakitin O.A. Unusual transformation of 3-alkylfuroxans into 3-(nitrooxyalkyl)furoxans on treatment with a mixture of nitric and sulfuric acids Russian Chemical Bulletin. 2016. V.65. N12. P.2901-2906. DOI: 10.1007/s11172-016-1675-6 WOS Scopus OpenAlex
88	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 Mendeleev Communications. 2016. V.26. N5. P.388-390. DOI: 10.1016/j.mencom.2016.09.007 WOS Scopus OpenAlex
89	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 Mendeleev Communications. 2016. V.26. N5. P.365-374. DOI: 10.1016/j.mencom.2016.09.001 WOS Scopus OpenAlex
90	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 Tetrahedron. 2016. V.72. N41. P.6191-6281. DOI: 10.1016/j.tet.2016.07.067 WOS Scopus OpenAlex
91	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 Synthesis-Stuttgart. 2016. V.49. N05. P.1103-1108. DOI: 10.1055/s-0036-1588616 WOS Scopus OpenAlex
92	Kucherenko A.S. , Gerasimchuk V.V. , Lisnyak V.G. , Nelyubina Y.V. , Zlotin S.G. Prolinamide‐Derived Ionic‐Liquid‐Supported Organocatalyst for Asymmetric Mono‐ and Bis‐Aldol Reactions in the Presence of Water European Journal of Organic Chemistry. 2015. V.2015. N25. P.5649-5654. DOI: 10.1002/ejoc.201500775 WOS Scopus OpenAlex
93	Kochetkov S.V. , Kucherenko A.S. , Zlotin S.G. Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst Mendeleev Communications. 2015. V.25. N3. P.168-170. DOI: 10.1016/j.mencom.2015.05.002 WOS Scopus OpenAlex
94	Konstantinova L.S. , Amelichev S.A. , Zlotin S.G. , Struchkova M.I. , Godovikova T.I. , Rakitin O.A. [1,4]Dithiino[2,3-c:5,6-c’ ]bis[1,2,5]oxadiazole di-N-oxide: synthesis and oxidation to mono- and bis-S-oxides Mendeleev Communications. 2015. V.25. N5. P.339-340. DOI: 10.1016/j.mencom.2015.09.006 WOS Scopus OpenAlex
95	Zharkov M.N. , Kuchurov I.V. , Fomenkov I.V. , Zlotin S.G. , Tartakovsky V.A. Nitration of glycoluril derivatives in liquid carbon dioxide Mendeleev Communications. 2015. V.25. N1. P.15-16. DOI: 10.1016/j.mencom.2015.01.004 WOS Scopus OpenAlex
96	Ananikov V.P. , Khokhlova E.A. , Egorov M.P. , Sakharov A.M. , Zlotin S.G. , Kucherov A.V. , Kustov L.M. , Gening M.L. , Nifantiev N.E. Organic and hybrid molecular systems Mendeleev Communications. 2015. V.25. N2. P.75-82. DOI: 10.1016/j.mencom.2015.03.001 WOS Scopus OpenAlex
97	Zlotin S.G. , Churakov A.M. , Luk’yanov O.A. , Makhova N.N. , Sukhorukov A.Y. , Tartakovsky V.A. Novel approaches to pharmacology-oriented and energy rich organic nitrogen–oxygen systems Mendeleev Communications. 2015. V.25. N6. P.399-409. DOI: 10.1016/j.mencom.2015.11.001 WOS Scopus OpenAlex
98	Lisnyak V.G. , Kucherenko A.S. , Valeev E.F. , Zlotin S.G. (1,2-Diaminoethane-1,2-diyl)bis(N-methylpyridinium) Salts as a Prospective Platform for Designing Recyclable Prolinamide-Based Organocatalysts Journal of Organic Chemistry. 2015. V.80. N19. P.9570-9577. DOI: 10.1021/acs.joc.5b01555 WOS Scopus OpenAlex
99	Konoplyannikov A.G. , Alekseenskiy A.E. , Zlotin S.G. , Smirnov B.B. , Kalsina S.S. , Lepehina L.A. , Semenkova I.V. , Agaeva E.V. , Baboyan S.B. , Rjumshina E.A. , Nosachenko V.V. , Konoplyannikov M.A. Detonation nanodiamond complexes with cancer stem cells inhibitors or paracrine products of mesenchymal stem cells as new potential medications Crystallography Reports. 2015. V.60. N5. P.763-767. DOI: 10.1134/s1063774515050041 WOS Scopus OpenAlex
100	Guskov A.A. , Kuchurov I.V. , Zlotin S.G. Relative permittivity of monocomponent and binary solutions of N2O5 in liquid CO2 and their activity in nitration of cellulose Russian Journal of Physical Chemistry B. 2015. V.9. N8. P.1130-1136. DOI: 10.1134/s1990793115080059 WOS Scopus OpenAlex

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