Solid-phase synthesis of C-terminal peptide amides from N-tetrachlorophthaloyl protected amino acids

被引：5

作者：

Cros, E ^{[1
]}

Planas, M ^{[1
]}

Mejías, X ^{[1
]}

Bardají, E ^{[1
]}

机构：

[1] Univ Girona, Dept Chem, Girona 17071, Spain

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 35期

关键词：

D O I：

10.1016/S0040-4039(01)01193-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A new strategy for solid-phase synthesis of C-terminal peptide amides based on the use of N-tetrachlorophthaloyl protected amino acids with acid-labile side-chain protection is described. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：6105 / 6107

页数：3

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