Articles - Sciact

Articles (232)

#	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	Kucherenko A.S. , Lisnyak V.G. , Kostenko A.A. , Kochetkov S.V. , Zlotin S.G. C2-Symmetric pyrrolidine-derived squaramides as recyclable organocatalysts for asymmetric Michael reactions Organic & Biomolecular Chemistry. 2016. V.14. N41. P.9751-9759. DOI: 10.1039/c6ob01606e WOS Scopus OpenAlex
83	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
84	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
85	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
86	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
87	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
88	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
89	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
90	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
91	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
92	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
93	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
94	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
95	Zavozin A.G. , Ignat'ev N.V. , Schulte M. , Zlotin S.G. Synthesis of novel tridentate pyrazole–bipyridine ligands for Co-complexes as redox-couples in dye-sensitized solar cells Tetrahedron. 2015. V.71. N45. P.8551-8556. DOI: 10.1016/j.tet.2015.09.032 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	Vereshchagin A.N. , Elinson M.N. , Anisina Y.E. , Ryzhkov F.V. , Goloveshkin A.S. , Bushmarinov I.S. , Zlotin S.G. , Egorov M.P. Pot, atom and step economic (PASE) synthesis of 5-isoxazolyl-5H-chromeno[2,3-b]pyridine scaffold Mendeleev Communications. 2015. V.25. N6. P.424-426. DOI: 10.1016/j.mencom.2015.11.008 WOS Scopus OpenAlex
99	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
100	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

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