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Vitaly A. Osyanin

Researcher at Samara State Technical University

Publications -  101
Citations -  681

Vitaly A. Osyanin is an academic researcher from Samara State Technical University. The author has contributed to research in topics: Chemistry & Pyran. The author has an hindex of 11, co-authored 89 publications receiving 521 citations. Previous affiliations of Vitaly A. Osyanin include Samara State University.

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Reactions of o-quinone methides with pyridinium methylides: a diastereoselective synthesis of 1,2-dihydronaphtho[2,1-b]furans and 2,3-dihydrobenzofurans.

TL;DR: A simple, general route to the 1,2-dihydronaphtho[2,1-b]furans and 2,3- dihydrobenzofurans substituted at C-2 by an acyl or aryl group, starting from phenolic Mannich bases and pyridinium ylides has been developed.
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Modern Trends of Organic Chemistry in Russian Universities

A. I. Konovalov, +84 more
TL;DR: In this paper, a review devoted to the scientific achievements of the departments of organic chemistry in higher schools of Russia within the past decade is presented, focusing on the recent years of the 1990s.
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Convenient one-step synthesis of 4-unsubstituted 2-amino-4H-chromene-2-carbonitriles and 5-unsubstituted 5H-chromeno[2,3-b]pyridine-3-carbonitriles from quaternary ammonium salts

TL;DR: In this article, DBU catalyzed synthesis of 4-unsubstituted 2-amino-4H-chromene-2-carbonitriles in water under reflux.
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Reaction of Push–Pull Enaminoketones and in Situ Generated ortho-Quinone Methides: Synthesis of 3-Acyl-4H-chromenes and 2-Acyl-1H-benzo[f]chromenes as Precursors for Hydroxybenzylated Heterocycles

TL;DR: A simple and efficient method for the synthesis of 4H-chromenes and 1H-benzo[f]chromenes containing a trifluoroacetyl or aroyl group in the pyran ring from o-quinone methide precursors and push-pull enaminoketones has been developed.
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Synthesis, in vitro and in vivo evaluation of 2-aryl-4H-chromene and 3-aryl-1H-benzo[f]chromene derivatives as novel α-glucosidase inhibitors.

TL;DR: It is shown that 2-aryl-4H-chromene core retains pharmacophore properties while being readily available synthetically as analogs of naturally occurring flavonoids with prominent α-glucosidase inhibitory properties.