HIGHLY ENANTIOSELECTIVE AND DIASTEREOSELECTIVE REDUCTION OF SULFUR-FUNCTIONALIZED CYCLIC-KETONES WITH BAKERS-YEAST

被引：27

作者：

FUJISAWA, T

YAMANAKA, K

MOBELE, BI

SHIMIZU, M

机构：

[1] Department of Chemistry for Materials, Mie University, Tsu, Mie

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 03期

关键词：

D O I：

10.1016/S0040-4039(00)92638-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Bakers' yeast reduction of 2-phenylthiocyclopentanone, 2-phenylthiocyclohexanone, and 2-phenylthio-2-cyclopentenone affords the corresponding (1S,2R)-2-phenylthiocycloalkanols in optically pure form and excellent diastereomeric excess.

引用

页码：399 / 400

页数：2