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41
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Kovalevsky R.
, Kucherenko A.
, Korlyukov A.A.
, Zlotin S.
Asymmetric Conjugate Addition of 3‐Hydroxychromen‐4‐Ones to Electron‐Deficient Olefins Catalyzed by Recyclable C2‐Symmetric Squaramide
Advanced Synthesis & Catalysis. 2021.
V.364. N2. P.426-439. DOI: 10.1002/adsc.202101019
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42
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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
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43
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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
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44
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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
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45
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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
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46
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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
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47
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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
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48
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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
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49
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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
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50
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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
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51
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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
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52
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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
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53
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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
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54
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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
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55
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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
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56
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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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57
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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
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58
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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
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59
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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
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60
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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
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