Synthetic studies of thiazoline and thiazolidine-containing natural products - 1. Phosphorus pentachloride-mediated thiazoline construction reaction

被引：42

作者：

Ino, A ^{[1
]}

Murabayashi, A ^{[1
]}

机构：

[1] Shionogi & Co Ltd, Aburahi Labs, Shiga 5203423, Japan

来源：

TETRAHEDRON | 1999年 / 55卷 / 34期

关键词：

thiazolines; cyclization; phosphorus halogen compounds;

D O I：

10.1016/S0040-4020(99)00582-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Phosphorus pentachloride effectively mediates the cyclization of N-acylcysteamine derivatives giving rise to thiazoline rings. Using this method, sterically hindered thiazoline analogs could be constructed and thus segment A (the left half) of micacocidin, a unique antimycoplasma antibiotic, was synthesized efficiently. (C) 1999 Elsevier Science Ltd. All rights reserved.

引用

页码：10271 / 10282

页数：12

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