INHIBITION OF BOTRYTIS-CINEREA BY NEW SESQUITERPENOID COMPOUNDS OBTAINED FROM THE REARRANGEMENT OF ISOCARYOPHYLLENE

被引：33

作者：

COLLADO, IG

ALEU, J

MACIASSANCHEZ, AJ

HERNANDEZGALAN, R

机构：

[1] Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Cádiz, Cádiz, Apdo. 40

来源：

JOURNAL OF NATURAL PRODUCTS | 1994年 / 57卷 / 06期

关键词：

D O I：

10.1021/np50108a009

中图分类号：

Q94 [植物学];

学科分类号：

071001 ;

摘要：

A careful study of the acid-catalyzed cyclization of isocaryophyllene has provided new information on the reaction mechanism. A novel sesquiterpene skeletal type has resulted from unusual rearrangements of isocaryophyllene. The alcohols ginsenol [9] and 4 beta,8 alpha,10,10-tetramethyl-11-hydroxytricyclo[6,2,1,0(4,11)]undecane [10] were found to inhibit the growth of Botrytis cinerea in vitro.

引用

页码：738 / 746

页数：9

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