V
V. V. Plemenkov
Researcher at Kazan Federal University
Publications - 17
Citations - 72
V. V. Plemenkov is an academic researcher from Kazan Federal University. The author has contributed to research in topics: Ene reaction & Diels–Alder reaction. The author has an hindex of 4, co-authored 17 publications receiving 58 citations. Previous affiliations of V. V. Plemenkov include Immanuel Kant Baltic Federal University.
Papers
More filters
Journal ArticleDOI
Synthesis of new decasubstituted pillar[5]arenes containing glycine fragments and their interactions with Bismarck brown Y
Dmitry N. Shurpik,Pavel L. Padnya,Liliya T. Basimova,Vladimir G. Evtugin,V. V. Plemenkov,Ivan I. Stoikov +5 more
TL;DR: In this article, a new water-soluble decasubstituted pillar-arenes containing glycine and glycylglycine fragments were synthesized and characterized.
Journal ArticleDOI
Progress in the Chemistry of Macrocyclic Meroterpenoids.
TL;DR: This review discusses the successes in the synthesis and practical application of both natural and synthetic macrocycles, and discusses the issues related to biomedical activity, processes of self-association and aggregation, and the formation of host–guest complexes of various classes of macrocyclic merotenoids.
Journal ArticleDOI
Synthesis of benzothiazine sulfonamides via heteroatomic Diels–Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes
TL;DR: In this paper, the reaction of 4-fluoro-N-sulfinylaniline with norbornene and norbornadiene has afforded the Diels-Alder adducts of benzothiazine structure that have been oxidized into the corresponding benzothiaine sulfonamides.
Journal ArticleDOI
Synthesis of benzo- ortho -thiazines S -oxides by Diels-Alder reaction of N -sulfinylanilines with norbornadiene
TL;DR: In this article, substituted N-sulfinylanilines acting as dienes in the Diels-Alder reaction with norbornadiene S-oxides of benzo-ortho-thiazines were obtained, which were oxidized into the corresponding S,S-dioxides belonging to the class of hybrid thiazinesulfonamide compounds.
Journal ArticleDOI
Synthesis of cyclic sulfonamides by reaction of N-Sulfinyl-3-(trifluoromethyl)aniline with Norbornenes
TL;DR: The cycloaddition occurred predominantly with participation of the S=N−C1=C6 fragment of N-sulfinyl-3-(trifluoromethyl)aniline and exclusively at the endo side of bicyclo[2.2.1]heptenes.