Synthesis and insect antifeedant activity of 2-substituted 2,3-dihydrofuran-3-ols and butenolides (part II).

被引：0
|
作者：
Gebbinck, EAK [1 ]
Stork, GA [1 ]
Jansen, BJM [1 ]
de Groot, A [1 ]
机构：
[1] Agr Univ Wageningen, Res Ctr, Organ Chem Lab, NL-6703 HB Wageningen, Netherlands
来源：
TETRAHEDRON | 1999年 / 55卷 / 36期
关键词：
alkylation; cyanohydrins; furanones; antifeedants;
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The introduction of a hydroxy group at C-13 of the clerodane skeleton is proposed as a strategy to potentially increase the antifeedant activity of simple analogs. This idea is applied to clerodane analogs with furan or butenolide type sidechains and therefore syntheses were developed for several types of 3-alkyl-substituted butenolides, 3-alkyl-substituted-3-hydroxybutenolides and 3-hydroxytetrahydrofuran derivatives. The antifeedant activity was tested on 5th instar larvae of Pieris brassicae. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码：11077 / 11094
页数：18
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