Synthesis of agarofuran antifeedants, part II: Stereoselective construction of the tetrahydrofuran ring

被引：0
|
作者：
Boyer, FD [1 ]
Ducrot, PH [1 ]
机构：
[1] INRA, Unite Phytopharm & Mediateurs Chim, F-78026 Versailles, France
来源：
SYNTHESIS-STUTTGART | 2000年 / 13期
关键词：
antifeedants; agarofuran; Wieland-Miescher ketone; heterocyclisation;
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
This paper describes how to manage the last steps of the synthetic scheme of agarofurans synthesis according to the configurations obtained at C-4a and C-6 during the functionalization of hexahydronaphthalenones derived from a Wieland-Misher ketone in order to obtain either cis- or trans-nor-agarofurans. Synthesis of nor-agarofurans 20, 24 and 29 are described.
引用
收藏
页码：1868 / 1877
页数：10
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