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学科主题: 氟化学 ; 生命有机化学
题名: Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-,4,4-difluoronojirimycin
其他题名: 高立体选择性地合成二氟亚甲基化的氮糖
作者: Wang RW(王若文) ; Qing FL(卿凤翎)
通讯作者: 卿凤翎
刊名: Org. Lett.
发表日期: 2005
卷: 7, 期:11, 页:2189-2192
收录类别: SCI
部门归属: 上海有机所元素有机; 东华大学
英文摘要: D-1,4,6-Trideoxy-4,4-difluoronojirimycin and L-1,4,6-trideoxy-4,4-difluoronojirimycin, a novel series of gem-4,4-difluoromethylenated azasugars, were synthesized from CF3CH2OH in 10 steps. A key step was the highly diastereoselective construction of the piperidine ring via reductive amination.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000229420400028
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/17549
Appears in Collections:中科院有机氟化学重点实验室_期刊论文

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Recommended Citation:
Wang RW,Qing FL. Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-,4,4-difluoronojirimycin[J]. Org. Lett.,2005,7(11):2189-2192.
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