Alexey R. Romanov
Russian Academy of Sciences
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Featured researches published by Alexey R. Romanov.
RSC Advances | 2016
A. Yu. Rulev; Alexey R. Romanov
This review focuses on the recent achievements and new developments in the synthesis of polyfluorinated aza-heterocycles based on fluorine-bearing enones and ynones published in the last decade.
Journal of Organic Chemistry | 2017
Vasiliy M. Muzalevskiy; Alexander Yu. Rulev; Alexey R. Romanov; E. V. Kondrashov; Igor A. Ushakov; V. A. Chertkov; Valentine G. Nenajdenko
A detailed study of the reaction of trifluoroacetylated acetylenes and aryl (alkyl) hydrazines was performed, aimed to the regioselective synthesis of 3- or 5-trifluoromethylated pyrazoles. It was found that the regioselectivity of reaction depends dramatically on the solvent nature. Highly polar protic solvents (hexafluoroisopropanol) favor the formation of 3-trifluoromethylpyrazoles. In contrast, when the reaction was performed in polar aprotic solvents (DMSO), the formation of their 5-CF3-substituted isomers was preferentially observed. Alternatively, the regioselective assembly of 3-CF3-substituted pyrazoles can be performed via two-step one-pot procedure. The reaction of trifluoromethylated ynones with aryl (alkyl) hydrazines in the presence of acidic catalysts leads to formation of the corresponding hydrazones. The latter can be smoothly transformed into 3-CF3-pyrazoles by treatment with a base. This solvent-switchable procedure was used for the preparation of such important drugs as Celebrex and SC-560 as well as their isomers in gram scale. The possible reaction mechanism is discussed.
Journal of Sulfur Chemistry | 2017
E. V. Kondrashov; Alexey R. Romanov; Igor A. Ushakov; Alexander Yu. Rulev
ABSTRACT A method for the synthesis of captodative sulfanyl enals, enones and enoates via nucleophilic vinylic substitution of corresponding halogen-bearing derivatives has been developed. The one-pot treatment of the haloenoates, haloenones or haloenals with thiols in the presence of organic base leads either to vicinal dithiosubstituted carbonyl-bearing compound or captodative systems with good to excellent yield. The major reaction direction strongly depends on the type of base used. GRAPHICAL ABSTRACT
Organic Letters | 2013
Alexander Yu. Rulev; Vasiliy M. Muzalevskiy; E. V. Kondrashov; Igor A. Ushakov; Alexey R. Romanov; Victor N. Khrustalev; Valentine G. Nenajdenko
Chemistry: A European Journal | 2015
V. M. Muzalevskiy; Yury A. Ustynyuk; Igor P. Gloriozov; V. A. Chertkov; Alexander Yu. Rulev; E. V. Kondrashov; Igor A. Ushakov; Alexey R. Romanov; Valentine G. Nenajdenko
Mendeleev Communications | 2014
Alexey R. Romanov; Alexander Yu. Rulev; Igor A. Ushakov; Vasiliy M. Muzalevskiy; Valentine G. Nenajdenko
Tetrahedron | 2014
N. N. Chipanina; Larisa P. Oznobikhina; T. N. Aksamentova; Alexey R. Romanov; A. Yu. Rulev
Journal of Organic Chemistry | 2016
Alexander Yu. Rulev; Alexey R. Romanov; E. V. Kondrashov; Igor A. Ushakov; Alexander V. Vashchenko; Vasiliy M. Muzalevskiy; Valentine G. Nenajdenko
European Journal of Organic Chemistry | 2016
V. M. Muzalevskiy; Alexander Yu. Rulev; E. V. Kondrashov; Alexey R. Romanov; Igor A. Ushakov; V. A. Chertkov; Valentine G. Nenajdenko
Tetrahedron | 2017
Alena I. Fedotova; Tatiana A. Komarova; Alexey R. Romanov; Igor A. Ushakov; Julien Legros; Jacques Maddaluno; Alexander Yu. Rulev