Highly stereoselective synthesis of trans,trans-4-aryl-2,3-oxetanedimethanols: Preparation of oxetanocin A analogues

被引:44
作者
Jung, ME
Nichols, CJ
机构
[1] Dept. of Chemistry and Biochemistry, University of California, Los Angeles
基金
美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/0040-4039(96)01720-0
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A short (5-step) synthesis of the oxetanocin A analogues 12a and 12b has been accomplished, with very good stereoselectivity in the key iodocyclization step. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:7667 / 7670
页数:4
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