Observations on the oxirane ring opening reactions of a 2-acetamido-3,4-anhydro sugar and on the inversion of the derived alcohols

被引：8

作者：

Banaszek, A ^{[1
]}

Janisz, B ^{[1
]}

机构：

[1] Polish Acad Sci, Inst Organ Chem, PL-01224 Warsaw, Poland

来源：

TETRAHEDRON-ASYMMETRY | 2000年 / 11卷 / 23期

关键词：

D O I：

10.1016/S0957-4166(00)00452-3

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A novel methodology for the preparation of L-enantiomers of 2,4- and 2,3-diacetamido-2,4,6- and 2,3,6-trideoxy-pyranoses is described. Factors influencing both the steric course of the epoxide ring opening and substitution are discussed. (C) 2001 Elsevier Science Ltd. All-rights reserved.

引用

页码：4693 / 4700

页数：8

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