A general and efficient procedure for the preparation of enantiopure anti-1,2-diols -: synthesis and utility of (R′,R′,S,R)-2,3-butane diacetal protected butane tetrol

被引：25

作者：

Dixon, DJ ^{[1
]}

Foster, AC ^{[1
]}

Ley, SV ^{[1
]}

Reynolds, DJ ^{[1
]}

机构：

[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1999年 / 12期

关键词：

D O I：

10.1039/a902732g

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The synthesis and utility of 2,3-butane diacetal protected butane tetrol (R',R',R,S)-2 for the general and efficient production of enantiopure anti-1,2-diols through selective silylation, alkylation and acetalisation of the spatially different hydroxy termini is described.

引用

页码：1635 / 1637

页数：3

共 15 条

[1]

Baeschlin DK, 1998, ANGEW CHEM INT EDIT, V37, P3423, DOI 10.1002/(SICI)1521-3773(19981231)37:24&lt

[2]

3423::AID-

[3] The alkylation of a novel acetal derived from (2R,3R)-(+)-tartaric acid:: An unexpected rearrangement [J].