THE STEREOCHEMICAL OUTCOME FROM MITSUNOBU COUPLINGS OF VICINAL, N-PROTECTED ACYCLIC AMINO-ALCOHOLS

被引：15

作者：

LIPSHUTZ, BH

MILLER, TA

机构：

[1] Department of Chemistry University of California, Santa Barbara

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 37期

关键词：

D O I：

10.1016/S0040-4039(00)98043-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Contrary to results expected in Mitsunobu reactions of amides derived from acyclic vic-amino alcohols (i.e., double inversion and hence, retention), urethane derivatives afford products solely of inversion. © 1990.

引用

页码：5253 / 5256

页数：4

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