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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2013 Volume 23, Issue 1, Pages 37–38 (Mi mendc2605)

This article is cited in 2 papers

Aryloxyacetamides Derived from Resveratroloside and Pinostilbenoside

A. V. Pozdeevaa, N. I. Komarovab, V. G. Vasilievb, A. D. Rogachevb, N. F. Salakhutdinovb, G. A. Tolstikovb

a Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: Etherification of phenolic hydroxyl groups of resveratroloside and pinostilbenoside (natural 3,4,5-trihydroxystilbene derivatives) with methyl bromoacetate afforded compounds ArOCH2CO2Me, which on treatment with amines produce the corresponding ‘stilbenyl- oxyacetamides’ in good yields.

Keywords: resveratrol, stilbene glycosides, Pinus sibirica, amides.

Language: English

DOI: 10.1016/j.mencom.2013.01.013



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