Synthesis of 6-deoxy-6-iodo-D-fructose

被引：4

作者：

Fellahi, M ^{[1
]}

Morin, C ^{[1
]}

机构：

[1] Univ Grenoble, CNRS, UMR 5616, LEDSS,Grp Marqueurs Biomed, F-38041 Grenoble, France

来源：

CARBOHYDRATE RESEARCH | 1999年 / 322卷 / 1-2期

关键词：

D-fructose; halogenation; acyclic hex-2-ulose; NMR; spectral simulation;

D O I：

10.1016/S0008-6215(99)00198-6

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

6-Deoxy-6-iodo-D-fructose was prepared from D-fructose by a three-step sequence involving partial acetylation, iodination to yield an acyclic D-arabino-hex-2-ulose derivative, followed by deprotection of the acetates. Structures were confirmed by simulation of H-1 NMR spectra.

引用

页码：142 / 146

页数：5

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