A versatile route to conjugated hydroxy (E,Z,E,E)-tetraenoic acids: highly chemo- and stereoselective synthesis of lipoxin B-4

被引：21

作者：

Alami, M ^{[1
]}

Crousse, B ^{[1
]}

Linstrumelle, G ^{[1
]}

Mambu, L ^{[1
]}

Larcheveque, M ^{[1
]}

机构：

[1] ECOLE NATL SUPER CHIM PARIS,URA 1381,SYNTH ORGAN LAB,F-75231 PARIS 05,FRANCE

来源：

TETRAHEDRON-ASYMMETRY | 1997年 / 8卷 / 17期

关键词：

D O I：

10.1016/S0957-4166(97)00333-9

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A highly convergent total stereocontrolled synthesis of lipoxin Bq is described by an efficient Pd-catalyzed coupling reaction of two easily accessible chiral synthons 2 and 3 without any protection-deprotection sequence of the alcohol functions. (C) 1997 Elsevier Science Ltd.

引用

页码：2949 / 2958

页数：10

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