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ANOMERIC SPIROHYDANTOINS OF MANNOFURANOSE - APPROACHES TO NOVEL ANOMERIC AMINO-ACIDS BY AN OXIDATIVE RING CONTRACTION

被引：47
作者：
BURTON, JW
SON, JC
FAIRBANKS, AJ
CHOI, SMS
TAYLOR, H
WATKIN, DJ
WINCHESTER, BG
FLEET, GWJ
机构：
[1] OXFORD CTR MOLEC SCI,DYSON PERRINS LAB,S PARKS RD,OXFORD OX1 3QY,ENGLAND
[2] UNIV OXFORD,CHEM CRYSTALLOG LAB,OXFORD OX1 3PD,ENGLAND
[3] UNIV LONDON,INST CHILD HLTH,LONDON WC1N 1EH,ENGLAND
来源：
TETRAHEDRON LETTERS | 1993年 / 34卷 / 38期
关键词：
D O I：
10.1016/S0040-4039(00)61745-8
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Bromine-induced oxidative ring contraction of an alpha-amino-delta-lactone gave a mixture of alpha-aminotetrahydrofurancarboxylic esters which may allow the preparation of stable amino acid derivatives at the anomeric position of mannofuranose. The synthesis of N-phenylhydantoins at the anomeric position of mannofuranose is reported.
引用
收藏
页码：6119 / 6122
页数：4
相关论文
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