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

页码：1868 / 1877

页数：10

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