Articles - Sciact

Articles (232)

#	Публикация
41	Vasil’ev A.A. , Burukin A.S. , Zhdankina G.M. , Zlotin S.G. Buchwald ligand-assisted Suzuki cross-coupling of polychlorobenzenes Mendeleev Communications. 2021. V.31. N3. P.400-402. DOI: 10.1016/j.mencom.2021.05.039 WOS OpenAlex
42	Kostenko A.A. , Kuznetsova O.Y. , Kucherenko A.S. , Zlotin S.G. Novel C2-symmetric phenylglycine derivatives as organocatalysts of the Michael reaction between nitroalkenes and ketones Russian Chemical Bulletin. 2021. V.70. N5. P.885-889. DOI: 10.1007/s11172-021-3163-x WOS Scopus OpenAlex
43	Vasil’ev A.A. , Burukin A.S. , Zhdankina G.M. , Zlotin S.G. Buchwald ligand-assisted Suzuki cross-coupling of polychlorobenzenes Mendeleev Communications. 2021. V.31. N3. P.400-402. DOI: 10.1016/j.mencom.2021.04.039 Scopus OpenAlex
44	Fauziev R.V. , Ivanov R.E. , Kuchurov I. , Zlotin S.G. A carbon dioxide-promoted three-component Strecker reaction Green Chemistry. 2021. V.23. N24. P.10137-10144. DOI: 10.1039/d1gc03161a WOS Scopus OpenAlex
45	Alekseev E.S. , Alentiev A.Y. , Belova A.S. , Bogdan V.I. , Bogdan T.V. , Bystrova A.V. , Gafarova E.R. , Golubeva E.N. , Grebenik E.A. , Gromov O.I. , Davankov V.A. , Zlotin S.G. , Kiselev M.G. , Koklin A.E. , Kononevich Y.N. , Lazhko A.E. , Lunin V.V. , Lyubimov S.E. , Martyanov O.N. , Mishanin I.I. , Muzafarov A.M. , Nesterov N.S. , Nikolaev A.Y. , Oparin R.D. , Parenago O.O. , Parenago O.P. , Pokusaeva Y.A. , Ronova I.A. , Solovieva A.B. , Temnikov M.N. , Timashev P.S. , Turova O.V. , Filatova E.V. , Philippov A.A. , Chibiryaev A.M. , Shalygin A.S. Supercritical fluids in chemistry Russian Chemical Reviews. 2020. V.89. N12. P.1337-1427. DOI: 10.1070/rcr4932 WOS Scopus OpenAlex
46	Pavlov V.A. , Shushenachev Y.V. , Zlotin S.G. Possible Physical Basis of Mirror Symmetry Effect in Racemic Mixtures of Enantiomers: From Wallach’s Rule, Nonlinear Effects, B–Z DNA Transition, and Similar Phenomena to Mirror Symmetry Effects of Chiral Objects Symmetry-Basel. 2020. V.12. N6. 889 . DOI: 10.3390/sym12060889 WOS Scopus OpenAlex
47	Zlotin S.G. , Banina O.A. , Sudarikov D.V. , Nigmatov A.G. , Frolova L.L. , Kutchin A.V. Asymmetric aldol reaction of isatins with acetone in the presence of terpene amino alcohols Mendeleev Communications. 2020. V.30. N2. P.147-149. DOI: 10.1016/j.mencom.2020.03.005 WOS Scopus OpenAlex
48	Zharkov M.N. , Kuchurov I.V. , Zlotin S.G. Micronization of CL-20 using supercritical and liquefied gases CrystEngComm. 2020. V.22. N44. P.7549-7555. DOI: 10.1039/d0ce01167c WOS Scopus OpenAlex
49	Tukhvatshin R.S. , Kucherenko A.S. , Nelyubina Y.V. , Zlotin S.G. Conjugate Addition of Carbon Acids to β,γ-Unsaturated α-Keto Esters: Product Tautomerism and Applications for Asymmetric Synthesis of Benzo[a]phenazin-5-ol Derivatives Journal of Organic Chemistry. 2019. V.84. N21. P.13824-13831. DOI: 10.1021/acs.joc.9b02021 WOS Scopus OpenAlex
50	Zharkov M.N. , Arabadzhi S.S. , Kuchurov I.V. , Zlotin S.G. Continuous nitration of alcohols in a Freon flow Reaction Chemistry & Engineering. 2019. V.4. N7. P.1303-1308. DOI: 10.1039/c9re00035f WOS Scopus OpenAlex
51	Pavlov V.A. , Shushenachev Y.V. , Zlotin S.G. Сhiral and Racemic Fields Concept for Understanding of the Homochirality Origin, Asymmetric Catalysis, Chiral Superstructure Formation from Achiral Molecules, and B-Z DNA Conformational Transition Symmetry-Basel. 2019. V.11. N5. 649 . DOI: 10.3390/sym11050649 WOS Scopus OpenAlex
52	Vinogradov M.G. , Turova O.V. , Zlotin S.G. Recent advances in the asymmetric synthesis of pharmacology-relevant nitrogen heterocyclesviastereoselective aza-Michael reactions Organic & Biomolecular Chemistry. 2019. V.17. N15. P.3670-3708. DOI: 10.1039/c8ob03034k WOS Scopus OpenAlex
53	Dobrynin O.S. , Zharkov M.N. , Kuchurov I.V. , Fomenkov I.V. , Zlotin S.G. , Monogarov K.A. , Meerov D.B. , Pivkina A.N. , Muravyev N.V. Supercritical Antisolvent Processing of Nitrocellulose: Downscaling to Nanosize, Reducing Friction Sensitivity and Introducing Burning Rate Catalyst Nanomaterials. 2019. V.9. N10. 1386 . DOI: 10.3390/nano9101386 WOS Scopus OpenAlex
54	Bykova K.A. , Kostenko A.A. , Kucherenko A.S. , Zlotin S.G. Asymmetric Michael reaction between aldehydes and nitroalkanes promoted by pyrrolidine-containing C2-symmetric organocatalysts Russian Chemical Bulletin. 2019. V.68. N7. P.1402-1406. DOI: 10.1007/s11172-019-2568-2 WOS OpenAlex
55	Kucherenko A.S. , Kostenko A.A. , Komogortsev A.N. , Lichitsky B.V. , Fedotov M.Y. , Zlotin S.G. C2-Symmetric Chiral Squaramide, Recyclable Organocatalyst for Asymmetric Michael Reactions Journal of Organic Chemistry. 2019. V.84. N7. P.4304-4311. DOI: 10.1021/acs.joc.9b00252 WOS Scopus OpenAlex
56	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
57	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
58	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
59	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
60	Kostenko A.A. , Kucherenko A.S. , Zlotin S.G. Recyclable C2-symmetric tertiary amine-squaramide organocatalysts: Design and application to asymmetric synthesis of γ-nitrocarbonyl compounds Tetrahedron. 2018. V.74. N36. P.4769-4776. DOI: 10.1016/j.tet.2018.07.043 WOS Scopus OpenAlex

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