Preparation of 1-(9-anthryl)-ethanol and 9-anthryloxirane via catalytic enantioselective reduction of prochiral 9-anthryl ketones

被引：13

作者：

Reiners, I ^{[1
]}

Martens, J ^{[1
]}

机构：

[1] UNIV OLDENBURG,FACHBEREICH CHEM,D-26129 OLDENBURG,GERMANY

来源：

TETRAHEDRON-ASYMMETRY | 1997年 / 8卷 / 01期

关键词：

D O I：

10.1016/S0957-4166(96)00476-4

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Enantioselective reduction of prochiral 9-anthryl ketones to the corresponding chiral alcohols proceeds with high enantiomeric excess. The chiral alcohol 1-(9-anthryl)-2-bromo-ethanol can be converted to the corresponding chiral oxirane. (C) 1996, Elsevier Science Ltd.

引用

页码：27 / 28

页数：2

共 18 条

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