Stereoconvergent synthesis of C1-C17 and C18-C25 fragments of bafilomycin A1

被引：24

作者：

Yadav, J. S. ^{[1
]}

Reddy, K. Bhaskar ^{[1
]}

Sabitha, G. ^{[1
]}

机构：

[1] Indian Inst Chem Technol, Organ Div, Hyderabad 500007, Andhra Pradesh, India

来源：

TETRAHEDRON | 2008年 / 64卷 / 08期

关键词：

bafilomycin A(1); intermediates; bicyclic precursor; aldol; vinyl stannane; vinyl iodide; Evans-aldol;

D O I：

10.1016/j.tet.2007.11.091

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The effective syntheses of the enantiomerically pure C(1)-C(17) and C(18)-C(25) fragments as promising synthetic intermediates of bafilomycin A(1), I have been achieved. (C) 2007 Published by Elsevier Ltd.

引用

页码：1971 / 1982

页数：12

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