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61
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Kucherenko A.
, Kostenko A.
, Zhdankina G.M.
, Kuznetsova O.Y.
, Zlotin S.G.
Green asymmetric synthesis of Warfarin and Coumachlor in pure water catalyzed by quinoline-derived 1,2-diamines
Green Chemistry. 2018.
V.20. N3. P.754-759. DOI: 10.1039/c7gc03626d
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62
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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
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63
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Pavlov V.A.
, Zlotin S.G.
Homochirality, Stochastic Chiral Reactions, Spontaneous Chiral Ordering of Achiral Molecules, and Similar Chiral Effects. Is there a Physical Basis for these Mirror Symmetry Breaking Phenomena?**
Current Organic Chemistry. 2018.
V.22. N21. P.2029-2054. DOI: 10.2174/1385272822666180910100449
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64
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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
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65
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Vereshchagin A.N.
, Elinson M.N.
, Anisina Y.E.
, Karpenko K.A.
, Goloveshkin A.S.
, Zlotin S.G.
, Egorov M.P.
High diastereoselective amine-catalyzed Knoevenagel–Michael-cyclization–ring-opening cascade between aldehydes, 3-arylisoxazol-5(4H)-ones and 3-aminocyclohex-2-en-1-ones
Molecular Diversity. 2018.
V.22. N3. P.627-636. DOI: 10.1007/s11030-018-9817-4
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66
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Ogurtsov V.A.
, Dorovatovskii P.V.
, Zubavichus Y.V.
, Khrustalev V.N.
, Fakhrutdinov A.N.
, Zlotin S.G.
, Rakitin O.A.
[1,2,5]Oxadiazolo[3,4-d]pyridazine 1,5,6-trioxides: efficient synthesis via the reaction of 3,4-bis(hydroxyimino)methyl)-1,2,5-oxadiazole 2-oxides with a mixture of concentrated nitric and trifluoroacetic acids and structural characterization
Tetrahedron Letters. 2018.
V.59. N32. P.3143-3146. DOI: 10.1016/j.tetlet.2018.07.015
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67
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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
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68
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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
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69
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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
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70
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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
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71
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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
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72
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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
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73
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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
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74
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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
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75
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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
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76
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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
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77
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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
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78
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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
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79
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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
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80
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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
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