Asymmetric synthesis of (2R,3S)-2,3-Epoxyamides via camphor-derived sulfonium ylides
Zhou YG(周永贵) ; Hou XL(侯雪龙) ; Dai LX(戴立信) ; Xia LJ(夏立钧) ; Tang MH(唐民华)
刊名J. Chem. Soc.-Perkin Trans. 1
1999
页码77-80
ISSN号0300-922X
其他题名经樟脑衍生的硫叶立德合成手性(2R,3S)-2,3-环氧酰胺
通讯作者侯雪龙
英文摘要Enantiomerically enriched trans-2,3-epoxyamides 3 were prepared by the reaction of aldehydes 2 with camphorderived chiral sulfonium ylide 1 in good yields and moderate to good eevalues. The absolute configuration of the reaction product is also determined by chemical transformations.
学科主题元素有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/a806189k
语种英语
WOS记录号WOS:000078128900011
公开日期2013-02-19
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/15819]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Zhou YG,Hou XL,Dai LX,et al. Asymmetric synthesis of (2R,3S)-2,3-Epoxyamides via camphor-derived sulfonium ylides[J]. J. Chem. Soc.-Perkin Trans. 1,1999:77-80.
APA 周永贵,侯雪龙,戴立信,夏立钧,&唐民华.(1999).Asymmetric synthesis of (2R,3S)-2,3-Epoxyamides via camphor-derived sulfonium ylides.J. Chem. Soc.-Perkin Trans. 1,77-80.
MLA 周永贵,et al."Asymmetric synthesis of (2R,3S)-2,3-Epoxyamides via camphor-derived sulfonium ylides".J. Chem. Soc.-Perkin Trans. 1 (1999):77-80.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace