共 43 条
Oxidative amide synthesis and N-terminal α-amino group ligation of peptides in aqueous medium
被引:167
作者:

Chan, Wing-Kei
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hong Kong, Dept Chem, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China

Ho, Chi-Ming
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hong Kong, Dept Chem, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China

Wong, Man-Kin
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hong Kong, Dept Chem, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China

Che, Chi-Ming
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hong Kong, Dept Chem, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China
机构:
[1] Univ Hong Kong, Dept Chem, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Open Lab Chem Biol, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China
关键词:
D O I:
10.1021/ja064479s
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A new method for oxidative synthesis of amides from alkynes and amines in high yields (up to 96%) using [Mn(2,6-Cl2TPP)Cl] 1 as a catalyst and Oxone/H2O2 as an oxidant in aqueous medium has been developed. This method could be used for N-terminal α-amino group ligation of unprotected peptides with aryl, aliphatic, and internal alkynes under mild conditions. Copyright © 2006 American Chemical Society.
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页码:14796 / 14797
页数:2
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