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多羟基吡咯烷衍生物的立体选择性合成
引用本文:李小六,田军,徐晓明,侯银菊. 多羟基吡咯烷衍生物的立体选择性合成[J]. 高等学校化学学报, 2006, 27(4): 660-665
作者姓名:李小六  田军  徐晓明  侯银菊
作者单位:1. 河北大学化学与环境科学学院, 保定 071002; 2. 南开大学元素有机化学国家重点实验室, 天津 300071
基金项目:中国科学院资助项目;河北省自然科学基金;国家重点实验室基金
摘    要:以D-木糖及D-葡萄糖为原料, 经具有降冰片结构的双环缩醛中间体, 合成了适当羟基保护的五元环氮杂糖衍生物及其氟代衍生物, 进一步探讨了含氮杂糖结构的双糖衍生物的合成.

关 键 词:氮杂糖   多羟基吡咯烷   氟代氮杂糖衍生物   低聚糖,
文章编号:0251-0790(2006)04-0660-06
收稿时间:2005-03-28
修稿时间:2005-03-28

Stereoselective Synthesis of Derivatives of Polyhydroxylated Pyrrolidines
LI Xiao-Liu,TIAN Jun,XU Xiao-Ming,HOU Yin-Ju. Stereoselective Synthesis of Derivatives of Polyhydroxylated Pyrrolidines[J]. Chemical Research In Chinese Universities, 2006, 27(4): 660-665
Authors:LI Xiao-Liu  TIAN Jun  XU Xiao-Ming  HOU Yin-Ju
Affiliation:1. School of Chemistry and Environmental Science, Hebei University, Baoding 071002, China;2. State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China
Abstract:The derivatives of polyhydroxylated pyrrolidines have exhibited a remarkable biological activity to inhibit glycoside-processing enzymes,and found a potential chemotherapeutic applications against diabetes,cancer,and viral infections including AIDS.And great attention has been attracted to the synthesis of their new derivatives and analogues.In this paper,some new derivatives of 5-membered azasugars with partially protected hydroxy groups,and their fluorinated ones were synthesized via the key intermediate of norbonyl like bicyclic acetal with D-xylose and Dglucose as the starting materials.The glycosylation of the synthesized partially protected azasugar and 1-methylenesugar was explored.
Keywords:Azasugar  Polyhydroxylated pyrrolidine  Fluorinated azasugar  Oligosaccharide
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