Synthesis of a thioester linker precursor for a general preparation of peptide C-terminal thioacids

被引:13
作者
Gaertner, H
Villain, M
Botti, P
Canne, L
机构
[1] Geneprot, CH-1217 Meyrin 2, Switzerland
[2] Gryphon Therapeut, San Francisco, CA 94080 USA
关键词
thioacids; thioesters; C-terminal modified peptides;
D O I
10.1016/j.tetlet.2003.12.160
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A general procedure to prepare peptide thioacids by solid-phase peptide synthesis is presented. The method involves the synthesis of 4-[alpha-(S-acetyl)mercaptobenzyl]phenoxyacetic acid as general precursor. This reagent once attached to a solid support is derivatized with the Boc-amino acid of choice after deprotection of the thiol. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2239 / 2241
页数:3
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