Convenient synthesis of a central 2,3,6-trisubstituted pyridine skeleton of a macrobicyclic antibiotic, cyclothiazomycin

被引：15

作者：

Okabe, A ^{[1
]}

Ito, A ^{[1
]}

Okumura, K ^{[1
]}

Shin, C ^{[1
]}

机构：

[1] Kanagawa Univ, Fac Technol, Organ Chem Lab, Kanagawa Ku, Yokohama, Kanagawa 2218686, Japan

来源：

CHEMISTRY LETTERS | 2001年 / 05期

关键词：

D O I：

10.1246/cl.2001.380

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The first convenient synthesis of the main central 2,3,6-trisubstituted pyridine skeleton [protected Fragment A-B] of a macrobicyclic antibiotic, cyclothiazomycin, was achieved.

引用

页码：380 / 381

页数：2

共 5 条

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