A. V. Pozdeeva, N. I. Komarova, V. G. Vasiliev, A. D. Rogachev, N. F. Salakhutdinov, G. A. Tolstikov, “Aryloxyacetamides Derived from Resveratroloside and Pinostilbenoside”, Mendeleev Commun., 23:1 (2013), 37

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Mendeleev Communications, 2013, Volume 23, Issue 1, Pages 37–38
DOI: https://doi.org/10.1016/j.mencom.2013.01.013 (Mi mendc2605)

This article is cited in 2 scientific papers (total in 2 papers)

Aryloxyacetamides Derived from Resveratroloside and Pinostilbenoside

A. V. Pozdeeva^a, N. I. Komarova^b, V. G. Vasiliev^b, A. D. Rogachev^b, N. F. Salakhutdinov^b, G. A. Tolstikov^b

^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

Full-text PDF (1067 kB) Citations (2) Supplementary materials

DOI: https://doi.org/10.1016/j.mencom.2013.01.013

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.

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Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(672.6 Kb)

Citation: A. V. Pozdeeva, N. I. Komarova, V. G. Vasiliev, A. D. Rogachev, N. F. Salakhutdinov, G. A. Tolstikov, “Aryloxyacetamides Derived from Resveratroloside and Pinostilbenoside”, Mendeleev Commun., 23:1 (2013), 37–38

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https://www.mathnet.ru/eng/mendc2605

https://www.mathnet.ru/eng/mendc/v23/i1/p37

This publication is cited in the following 2 articles:

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