Synthesis of a model of chloropeptins I, II western subunit by the intramolecular SNAr based methodology

被引：15

作者：

Roussi, G

Zamora, EG

Carbonnelle, AC

Beugelmans, R

机构：

[1] Inst. Chim. Substances Naturelles, CNRS, 91198, Gif-sur-Yvette

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 25期

关键词：

D O I：

10.1016/S0040-4039(97)00938-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Formation of a biaryl ether bond between the termini of a tetrapeptide containing a highly racemization prone amino acid by the intramolecular SNAr reaction afforded two diastereomeric 16-membered macrocycles along with their respective atropoisomers. The (R,S,R) and its atropoisomer constituted a model of chloropeptins I, II western part. (C) 1997 Published by Elsevier Science Ltd.

引用

页码：4401 / 4404

页数：4

共 13 条

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