Design and synthesis of a new class of arginine analogues with an improved anion binding site in the side chain

被引：25

作者：

Schmuck, C ^{[1
]}

Geiger, L ^{[1
]}

机构：

[1] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany

来源：

CHEMICAL COMMUNICATIONS | 2005年 / 06期

关键词：

D O I：

10.1039/b415543b

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Replacing the guanidinium group in arginine ( 1) by a guanidiniocarbonyl pyrrole moiety provides a new class of artificial amino acids ( 2), that can be used as building blocks in standard solid phase peptide synthesis.

引用

页码：772 / 774

页数：3

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