Synthesis of D-arabinohydroxamic acid and D-threonohydroxamic acid, potent inhibitors of D-xylose isomerases

被引：2
|
作者：
Gaudemer, A
Fanet, C
Gaudemer, F
Salmon, L
机构：
[1] Lab. Chim. Bioorganique B., Inst. de Chim. Molec. d'Orsay, Université de Paris-Sud
来源：
TETRAHEDRON LETTERS | 1996年 / 37卷 / 13期
关键词：
D O I：
10.1016/0040-4039(96)00254-7
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Two potent inhibitors of D-xylose isomerases: D-threonohydroxamic acid 2 and D-arabinohydroxamic acid 3 have been synthesized by conversion of D-arabinose to a protected derivative of D-arabinonic acid and introduction of the hydroxamate group by coupling with O-benzylhydroxylamine.
引用
收藏
页码：2237 / 2240
页数：4
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