Issue 7, 1977
From the journal:

Journal of the Chemical Society, Chemical Communications

Oxidative dimerisation of 4-hydroxystilbenes in vitro: production of a grapevine phytoalexin mimic

Peter Langcake  and  Robert J. Pryce  

Abstract

Dimerisation of trans-4-hydroxystilbenes with horseradish peroxidase–hydrogen peroxide gives analogous products to those formed from phenylpropenoids; the product (IX) obtained from trans-resveratrol is structurally related to the phytoalexin (I) isolated from grapevines but the coupling orientation is different, and both the natural and synthetic dimers of resveratrol have a similar spectrum of antifungal activity.

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Article information

DOI
https://doi.org/10.1039/C39770000208
Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 208-210

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Oxidative dimerisation of 4-hydroxystilbenes in vitro: production of a grapevine phytoalexin mimic

P. Langcake and R. J. Pryce, J. Chem. Soc., Chem. Commun., 1977, 208 DOI: 10.1039/C39770000208

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