Articles - Sciact

Articles (232)

#	Публикация
61	Filatova E.V. , Turova O.V. , Nigmatov A.G. , Zlotin S.G. Green asymmetric synthesis of tetrahydroquinolines in carbon dioxide medium promoted by lipophilic bifunctional tertiary amine – squaramide organocatalysts Tetrahedron. 2018. V.74. N1. P.157-164. DOI: 10.1016/j.tet.2017.11.057 WOS Scopus OpenAlex
62	Kuchurov I.V. , Arabadzhi S.S. , Zharkov M.N. , Fershtat L.L. , Zlotin S.G. Sustainable Synthesis of Polynitroesters in the Freon Medium and their in Vitro Evaluation as Potential Nitric Oxide Donors ACS Sustainable Chemistry & Engineering. 2018. V.6. N2. P.2535-2540. DOI: 10.1021/acssuschemeng.7b04029 WOS Scopus OpenAlex
63	Tukhvatshin R.S. , Kucherenko A.S. , Nelyubina Y.V. , Zlotin S.G. Stereoselective Synthesis of Tetrahydroquinolines via Asymmetric Domino Reaction Catalyzed by a Recyclable Ionic‐Liquid‐Supported Bifunctional Tertiary Amine European Journal of Organic Chemistry. 2018. V.2018. N48. P.7000-7008. DOI: 10.1002/ejoc.201801423 WOS Scopus OpenAlex
64	Konstantinova L.S. , Knyazeva E.A. , Gatilov Y.V. , Zlotin S.G. , Rakitin O.A. Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release Russian Chemical Bulletin. 2018. V.67. N1. P.95-101. DOI: 10.1007/s11172-018-2042-6 WOS Scopus OpenAlex
65	Kochetkov S.V. , Kucherenko A. , Zlotin S.G. Asymmetric synthesis of warfarin and its analogs catalyzed by C2-symmetric squaramide-based primary diamines Organic & Biomolecular Chemistry. 2018. V.16. N35. P.6423-6429. DOI: 10.1039/c8ob01576g WOS Scopus OpenAlex
66	Kostenko A.A. , Kucherenko A.S. , Komogortsev A.N. , Lichitsky B.V. , Zlotin S.G. Asymmetric Michael addition between kojic acid derivatives and unsaturated ketoesters promoted by C2-symmetric organocatalysts Organic & Biomolecular Chemistry. 2018. V.16. N48. P.9314-9318. DOI: 10.1039/c8ob02523a WOS Scopus OpenAlex
67	Vasil’ev A.A. , Kuchurov I.V. , Zlotin S.G. 1,4-cis-Hydrogenation of butyl sorbate in supercritical carbon dioxide Russian Chemical Bulletin. 2018. V.67. N5. P.923-926. DOI: 10.1007/s11172-018-2158-8 WOS Scopus OpenAlex
68	Obruchnikova N.V. , Novikov R.A. , Zlotin S.G. , Dorovatovskii P.V. , Khrustalev V.N. , Rakitin O.A. Synthesis and structural investigation of 4,4′-dimethyl-[3,3′-bi(1,2,5-oxadiazole)] 5,5′-dioxide Russian Chemical Bulletin. 2018. V.67. N11. P.2044-2048. DOI: 10.1007/s11172-018-2326-x WOS Scopus OpenAlex
69	Banina O.A. , Sudarikov D.V. , Nigmatov A.G. , Frolova L.L. , Slepukhin P.A. , Zlotin S.G. , Kutchin A.V. Carane amino alcohols as organocatalysts in asymmetric aldol reaction of isatin with acetone Russian Chemical Bulletin. 2017. V.66. N2. P.293-296. DOI: 10.1007/s11172-017-1730-y WOS Scopus OpenAlex
70	Troitskaya-Markova N.A. , Vlasova O.G. , Godovikova T.I. , Zlotin S.G. , Rakitin O.A. Bis[1,2,5]oxadiazolo[3,4- c :3’,4’- e ]pyridazine 4,5-dioxide as a synthetic equivalent of 4,4’-dinitroso-3,3’-bifurazan Mendeleev Communications. 2017. V.27. N5. P.448-450. DOI: 10.1016/j.mencom.2017.09.005 WOS Scopus OpenAlex
71	Zlotin S.G. , Churakov A.M. , Dalinger I.L. , Luk’yanov O.A. , Makhova N.N. , Sukhorukov A.Y. , Tartakovsky V.A. Recent advances in synthesis of organic nitrogen–oxygen systems for medicine and materials science Mendeleev Communications. 2017. V.27. N6. P.535-546. DOI: 10.1016/j.mencom.2017.11.001 WOS Scopus OpenAlex
72	Kochetkov S.V. , Kucherenko A.S. , Zlotin S.G. Asymmetric Michael addition of aldehydes to maleimides in primary amine-based aqueous ionic liquid-supported recyclable catalytic system Mendeleev Communications. 2017. V.27. N5. P.473-475. DOI: 10.1016/j.mencom.2017.09.014 WOS Scopus OpenAlex
73	Gerasimchuk V.V. , Kucherenko A.S. , Fakhrutdinov A.N. , Medvedev M.G. , Nelyubina Y.V. , Zlotin S.G. Towards Sustainable Amino Acid Derived Organocatalysts for Asymmetric syn‐Aldol Reactions European Journal of Organic Chemistry. 2017. V.2017. N17. P.2540-2544. DOI: 10.1002/ejoc.201700166 WOS Scopus OpenAlex
74	Gerasimchuk V.V. , Romanov R.R. , Woo G.H.-T. , Dmitriev I.A. , Kucherenko A.S. , Zlotin S.G. Novel L-threonine-based ionic liquid supported organocatalyst for asymmetric syn-aldol reaction: activity and recyclability design Arkivoc. 2017. N3. P.241-249. DOI: 10.24820/ark.5550190.p010.149 WOS Scopus OpenAlex
75	Vinogradov M.G. , Turova O.V. , Zlotin S.G. Nazarov reaction: current trends and recent advances in the synthesis of natural compounds and their analogs Organic & Biomolecular Chemistry. 2017. V.15. N39. P.8245-8269. DOI: 10.1039/c7ob01981e WOS Scopus OpenAlex
76	Ananikov V.P. , Eremin D.B. , Yakukhnov S.A. , Dilman A.D. , Levin V.V. , Egorov M.P. , Karlov S.S. , Kustov L.M. , Tarasov A.L. , Greish A.A. , Shesterkina A.A. , Sakharov A.M. , Nysenko Z.N. , Sheremetev A.B. , Stakheev A.Y. , Mashkovsky I.S. , Sukhorukov A.Y. , Ioffe S.L. , Terent’ev A.O. , Vil V.A. , Tomilov Y.V. , Novikov R.A. , Zlotin S.G. , Kucherenko A.S. , Ustyuzhanina N.E. , Krylov V.B. , Tsvetkov Y.E. , Gening M.L. , Nifantiev N.E. Organic and hybrid systems: from science to practice Mendeleev Communications. 2017. V.27. N5. P.425-438. DOI: 10.1016/j.mencom.2017.09.001 WOS Scopus OpenAlex
77	Kuchurov I.V. , Zharkov M.N. , Fershtat L.L. , Makhova N.N. , Zlotin S.G. Prospective Symbiosis of Green Chemistry and Energetic Materials ChemSusChem. 2017. V.10. N20. P.3914-3946. DOI: 10.1002/cssc.201701053 WOS Scopus OpenAlex
78	Sukhanova A.A. , Puchkin I.A. , Vasil'ev A.A. , Zlotin S.G. Synthesis and stereochemical assignment of geraniol- and nerol-derived Cygerol enantiomers Tetrahedron: Asymmetry. 2017. V.28. N12. P.1834-1841. DOI: 10.1016/j.tetasy.2017.10.024 OpenAlex
79	Tukhvatshin R.S. , Kucherenko A.S. , Nelyubina Y.V. , Zlotin S.G. Tertiary Amine-Derived Ionic Liquid-Supported Squaramide as a Recyclable Organocatalyst for Noncovalent “On Water” Catalysis ACS Catalysis. 2017. V.7. N4. P.2981-2989. DOI: 10.1021/acscatal.7b00562 WOS Scopus OpenAlex
80	Kucherenko A.S. , Kostenko A.A. , Gerasimchuk V.V. , Zlotin S.G. Stereospecific diaza-Cope rearrangement as an efficient tool for the synthesis of DPEDA pyridine analogs and related C2-symmetric organocatalysts Organic & Biomolecular Chemistry. 2017. V.15. N33. P.7028-7033. DOI: 10.1039/c7ob01852e WOS Scopus OpenAlex

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