SIOC OpenIR  > 中科院天然产物有机化学重点实验室
1,3-Dipolar cycloaddition of chirally modified vinylboronic ester with nitrile oxides
Alternative Title手性烯基硼酸酯与氰氧化物的 1,3-偶极环加成反应
Zhang A(张翱); Kan Y(阚颖); Zhao GL(赵桂玲); Jiang B(姜标)
2000
Source PublicationTetrahedron
ISSN0040-4020
Volume56Issue:7Pages:965-970
AbstractChiral 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.
Subject Area有机化学
Department中国科学院上海有机化学研究所现代有机化学实验室
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Indexed BySCI
Language英语
WOS IDWOS:000085305800004
Citation statistics
Cited Times:18[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/20095
Collection中科院天然产物有机化学重点实验室
Corresponding AuthorJiang B(姜标)
Recommended Citation
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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