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
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
收藏
页码:6105 / 6107
页数:3
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