SIOC OpenIR  > 中科院有机氟化学重点实验室
Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-,4,4-difluoronojirimycin
Alternative Title高立体选择性地合成二氟亚甲基化的氮糖
Wang RW(王若文); Qing FL(卿凤翎)
2005
Source PublicationOrg. Lett.
ISSN1523-7060
Volume7Issue:11Pages:2189-2192
AbstractD-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.
Subject Area氟化学 ; 生命有机化学
Department上海有机所元素有机; 东华大学
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Indexed BySCI
Language英语
WOS IDWOS:000229420400028
Citation statistics
Cited Times:36[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/17549
Collection中科院有机氟化学重点实验室
Corresponding AuthorQing FL(卿凤翎)
Recommended Citation
GB/T 7714
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.
APA 王若文,&卿凤翎.(2005).Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-,4,4-difluoronojirimycin.Org. Lett.,7(11),2189-2192.
MLA 王若文,et al."Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-,4,4-difluoronojirimycin".Org. Lett. 7.11(2005):2189-2192.
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