The Synthesis of an Exhaustively Stereodiversified Library of <i>cis</i>-1,5 Enediols by Silyl-Tethered Ring-Closing Metathesis
作者:Bryce A. Harrison、Gregory L. Verdine
DOI:10.1021/ol0159569
日期:2001.7.1
[reaction: see text] This report describes the parallel synthesis of all 16 stereoisomers of the cis-1,5 enediol module 1. Compounds 1 derive from 2 by silicon-tethered ring-closing metathesis. Such libraries of stereodiversified ligands provide a unique approach to ligand discovery that employs exhaustive searching of conformational space.
[反应:参见文本]该报告描述了顺式1,5烯二醇模块1的所有16种立体异构体的平行合成。化合物1通过硅束缚的开环复分解反应从2衍生而来。这种立体多样化配体的文库提供了独特的方法来进行配体发现,该方法采用了构象空间的详尽搜索。