Synthesis of N-alkyl substituted iminosugars from D-ribose

被引：0

作者：

Haibo Wang ^{[1
,2
,3
]}

Yang Pan ^{[1
,3
]}

Qin Tang ^{[1
,3
]}

Wei Zou ^{[4
]}

Huawu Shao ^{[1
]}

机构：

[1] Natural Products Research Center, Chengdu Institute of Biology, Chinese Academy of Sciences

[2] Zhejiang Hongyuan Pharmaceutical Co.,Ltd.

[3] Graduate School of Chinese Academy of Sciences

[4] Institute for Biological Sciences, National Research Council of Canada

来源：

ChineseChemicalLetters | 2018年 / 29卷 / 01期

基金：

中国国家自然科学基金;

关键词：

Iminosugar; Pyrrolidine; Piperidine; Glycosidase; D-Ribose;

D O I：

暂无

中图分类号：

TQ460.1 [基础理论];

学科分类号：

摘要：

An effective and facile method for the synthesis of N-alkylated hydroxylpyrrolidine and hydroxylpiperidine is described. A number of N-alkyl substituted iminosugars were prepared using iodine-induced intramolecular cyclization of acyclic alkenylamines as key step.

引用

页码：73 / 75

页数：3

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