Search Results - "Pokrovskii, Mikhail A."

Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents by Mironov, Maksim E., Rybalova, Tatyana V., Pokrovskii, Mikhail A., Emaminia, Fatemeh, Gandalipov, Erik R., Pokrovskii, Andrey G., Shults, Elvira E.

“…[Display omitted] •Selective synthesis of 6-(4ʹ-benzoyl-5ʹ-aryl-1ʹ,2ʹ,3ʹ-triazol-1ʹ-yl)spirostan-3β,5-diols by the three component reaction of…”
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6-(4′-Aryl-1′,2′,3′-triazolyl)-spirostan-3,5-diols and 6-(4′-Aryl-1′,2′,3′-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity by Mironov, Maxim E., Oleshko, Olga S., Pokrovskii, Mikhail A., Rybalova, Tatyana V., Pechurov, Vladislav K., Pokrovskii, Andrey G., Cheresis, Sergey V., Mishinov, Sergey V., Stupak, Vyacheslav V., Shults, Elvira E.

“…[Display omitted] •A selective methodology for the introduction of azido function in C-6 position and a hydroxyl substituent in C-5 or C-7 position of…”
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Aminocarbonylation of 2-(N-substituted) 5-iodobenzoates: synthesis of glyoxylamido-anthranilates, their cytotoxicity and molecular modeling study by Cheremnykh, Kirill P., Baev, Dmitry S., Nacharova, Elizaveta A., Pokrovskii, Mikhail A., Savelyev, Victor A., Meshkova, Yulia V., Marenina, Mariya K., Tolstikova, Tatyana G., Pokrovskii, Andrey G., Shults, Elvira E.

“…The aminocarbonylation of ethyl 2-substituted 5-iodobenzoate has been investigated in the presence of a series of amine nucleophiles, providing an efficient…”
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Design, synthesis, cytotoxicity, and molecular modeling study of 2,4,6-trisubstituted pyrimidines with anthranilate ester moiety by Cheremnykh, Kirill P., Savelyev, Victor A., Pokrovskii, Mikhail A., Baev, Dmitry S., Tolstikova, Tatyana G., Pokrovskii, Andrey G., Shults, Elvira E.

“…A series of 2,4,6-trisubstituted pyrimidines with antharanilic acid ester moiety have been designed and synthesized by employing a one-pot multicomponent…”
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Design and Synthesis of 3‐(N‐Substituted)aminocoumarins as Anticancer Agents from 3‐Bromopeuruthenicin by Lipeeva, Alla V., Zakharov, Danila O., Gatilov, Yurii V., Pokrovskii, Mikhail A., Pokrovskii, Andrey G., Shults, Elvira E.

“…A convenient protocol for the rapid and efficient synthesis of 3‐bromopeuruthenicin 2 from plant coumarin peuruthenicin 1 is described. Coumarin 2 have been…”
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