Ruthenium-promoted diaryl ether synthesis in the construction of the F-O-G ring system of a teicoplanin model

被引：21

作者：

Pearson, AJ ^{[1
]}

Belmont, PO ^{[1
]}

机构：

[1] Case Western Reserve Univ, Dept Chem, Cleveland, OH 44106 USA

来源：

TETRAHEDRON LETTERS | 2000年 / 41卷 / 11期

基金：

美国国家卫生研究院;

关键词：

D O I：

10.1016/S0040-4039(00)00030-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

An end-game approach is described for the synthesis of glycopeptide antibiotics related to teicoplanin, using ruthenium-promoted diaryl ether formation, followed by cycloamidation. (C) 2000 Elsevier Science Ltd. All rights reserved.

引用

页码：1671 / 1675

页数：5

共 42 条

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