Solid-phase synthesis of apicidin A and a cyclic tetrapeptoid analogue

被引：13
|
作者：
Berst, F
Ladlow, M
Holmes, AB
机构：
[1] GSK Cambridge Technol Ctr, Cambridge CB2 1EW, England
[2] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
来源：
CHEMICAL COMMUNICATIONS | 2002年 / 05期
关键词：
D O I：
10.1039/b110068h
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The solid-phase synthesis of the antiprotozoal cyclic tetrapeptide apicidin A is reported and its synthetic accessibility is contrasted with that of a structurally similar reduced cyclic tetrapeptoid analogue.
引用
收藏
页码：508 / 509
页数：2
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