1,3-Dipolar cycloaddition of chirally modified vinylboronic ester with nitrile oxides
Zhang A(张翱) ; Kan Y(阚颖) ; Zhao GL(赵桂玲) ; Jiang B(姜标)
刊名Tetrahedron
2000
卷号56期号:7页码:965-970
ISSN号0040-4020
其他题名手性烯基硼酸酯与氰氧化物的 1,3-偶极环加成反应
通讯作者姜标
英文摘要Chiral modified vinylboronic ester 1, derived from D-(+)-mannitol, reacted with nitrie oxides to afford optically active isoxazolines. The regioselectivity was excellent and moderate stereoselectivity (up to 60% d.e.) was achieved. The configuration of new chiral centres in all the isoxazoline products was estabilshed by NMR analysis or X-ray analysis.
学科主题有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/S0040-4020(00)00017-X
语种英语
WOS记录号WOS:000085305800004
公开日期2013-02-25
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/20095]  
专题上海有机化学研究所_中科院天然产物有机化学重点实验室
推荐引用方式
GB/T 7714
Zhang A,Kan Y,Zhao GL,et al. 1,3-Dipolar cycloaddition of chirally modified vinylboronic ester with nitrile oxides[J]. Tetrahedron,2000,56(7):965-970.
APA 张翱,阚颖,赵桂玲,&姜标.(2000).1,3-Dipolar cycloaddition of chirally modified vinylboronic ester with nitrile oxides.Tetrahedron,56(7),965-970.
MLA 张翱,et al."1,3-Dipolar cycloaddition of chirally modified vinylboronic ester with nitrile oxides".Tetrahedron 56.7(2000):965-970.
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