Preparation of chiral 1,3 skipped anti- and syn-tetrols via highly enantioselective biocatalytic resolution

被引：10

作者：

Bonini, C ^{[1
]}

Chiummiento, L ^{[1
]}

Funicello, M ^{[1
]}

机构：

[1] Univ Basilicata, Dipartimento Chim, I-85100 Potenza, Italy

来源：

TETRAHEDRON-ASYMMETRY | 2001年 / 12卷 / 19期

关键词：

D O I：

10.1016/S0957-4166(01)00467-0

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Biocatalytic resolution of the 7-benzyloxy-3,5-anti-dioxolan-1,3 5,7-tetrol and the 7-benzyloxy-3,5-syn-dioxolan-1,3,5,7-tetrol was found to be highly enantioselective leading to differently functionalized chiral tetrols with significantly high e.e. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：2755 / 2760

页数：6

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