Acylated derivatives of resveratrol and isoliquiritigenin
Abstract
Derivatives of resveratrol and isoliquiritigenin (esters of acetic, benzoic and succinic acid) have been synthesized and characterized. The hydroxy group in 2,-position of isoliquiritigenin is acylated more readily than at positions 4 and 4, that can be explained by the influence of the intramolecular hydrogen bond. Isoliquiritigenin and its derivatives with free 2,-hydroxyl undergo cycloisomerisation during gas chromatography analysis.
About the Authors
N. V. Kot
биоорганической химии НАН Беларуси
Belarus
Belarus
M. A. Kisel
биоорганической химии НАН Беларуси
Belarus
Belarus
P. V. Kurman
биоорганической химии НАН Беларуси
Belarus
Belarus
A. L. Mikhal’Chuk
биоорганической химии НАН Беларуси
Belarus
Belarus
V. V. Shylau
биоорганической химии НАН Беларуси
Belarus
Belarus
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