Stereoselective synthesis of conjugated all-trans-tetraenes. Application to the synthesis of beta-parinaric acid methyl ester.

被引：10

作者：

Solladie, G

Kalai, C

Adamy, M

Colobert, F

机构：

[1] Lab. de Stereochim. Associe au CNRS, ECPM, Université Louis Pasteur, 67008-Strasbourg

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 39期

关键词：

D O I：

10.1016/S0040-4039(97)01594-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

in this paper is reported the stereoselective synthesis of all-trans-tetraenes by reductive elimination of 1,8-dibenzoate-2,4,6-trienes with sodium amalgam. The method was applied to the syntheses of 4E, 6E, 8E, 10E-heptatetraene and beta-parinaric acid methyl ester. (C) 1997 Elsevier Science Ltd.

引用

页码：6917 / 6920

页数：4

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