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Статьи (232)

# Публикация
41 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
42 Zlotin S.G. , Churakov A.M. , Egorov M.P. , Fershtat L.L. , Klenov M.S. , Kuchurov I.V. , Makhova N.N. , Smirnov G.A. , Tomilov Y.V. , Tartakovsky V.A.
Advanced energetic materials: novel strategies and versatile applications
Mendeleev Communications. 2021. V.31. N6. P.731-749. DOI: 10.1016/j.mencom.2021.11.001 WOS Scopus OpenAlex
43 Ivanov R.E. , Zharkov M.N. , Zlotin S.G.
Nitration of Alkenes and Oxiranes with Nitrogen(IV) Oxide in Liquid and Supercritical Carbon Dioxide Media
Doklady Chemistry. 2021. V.500. N2. P.209-212. DOI: 10.1134/s0012500821100037 WOS Scopus OpenAlex
44 Vinogradov M.G. , Turova O.V. , Zlotin S.G.
Catalytic Asymmetric Aza‐Diels‐Alder Reaction: Pivotal Milestones and Recent Applications to Synthesis of Nitrogen‐Containing Heterocycles
Advanced Synthesis & Catalysis. 2021. V.363. N6. P.1466-1526. DOI: 10.1002/adsc.202001307 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 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 WOS Scopus OpenAlex
57 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 WOS Scopus OpenAlex
58 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 WOS Scopus OpenAlex
59 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 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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