Towards the stereochemical assignment of natural lydiamycin A

被引：30

作者：

Chen, Bo ^{[1
]}

Dai, Lu ^{[1
]}

Zhang, Hui ^{[1
]}

Tan, Wenfei ^{[1
]}

Xu, Zhengshuang ^{[1
,2
]}

Ye, Tao ^{[1
,2
]}

机构：

[1] Univ Town Shenzhen, Shenzhen Grad Sch, Peking Univ, Lab Chem Genom, Shenzhen 518055, Peoples R China

[2] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China

来源：

CHEMICAL COMMUNICATIONS | 2010年 / 46卷 / 04期

关键词：

ACYL ISOPEPTIDE METHOD; SEQUENCE-CONTAINING PEPTIDES; EFFICIENT SYNTHESIS; (3S)-2,3,4,5-TETRAHYDROPYRIDAZINE-3-CARBOXYLIC ACID; ABSOLUTE-CONFIGURATION; MATLYSTATIN-B; ANALOGS; TUBERCULOSIS; CYCLODEPSIPEPTIDE; MIGRATION;

D O I：

10.1039/b922544g

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A convergent approach leading to the stereoselective synthesis of four diastereomers of lydiamycin A has been established and verified.

引用

页码：574 / 576

页数：3

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