中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Pd-Catalyzed Diastereo- and Enantioselective [3+2]-Cycloaddition Reaction of Vinyl Epoxide with Nitroalkenes

文献类型:期刊论文

作者Wu WQ(武文琼) ; Ding CH(丁昌华) ; Hou XL(侯雪龙)
刊名Synlett
出版日期2012
期号7页码:1035-1038
ISSN号0936-5214
其他题名钯催化烯基环氧和硝基烯烃的非对映及对映选择性[3+2]环加成反应
通讯作者侯雪龙
英文摘要A diastereoselective and enantioselective [3+2]-cycloaddition reaction of vinyl epoxide and nitroalkenes has been developed using Pd/1,1'-ferrocene-P, N-ligand, providing substituted tetrahydrofurans in high yields and with high diastereo- and enantioselectivities.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1055/s-0031-1290525
语种英语
WOS记录号WOS:000302858500010
公开日期2013-08-22
源URL[http://202.127.28.38/handle/331003/28009]  
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
Wu WQ,Ding CH,Hou XL. Pd-Catalyzed Diastereo- and Enantioselective [3+2]-Cycloaddition Reaction of Vinyl Epoxide with Nitroalkenes[J]. Synlett,2012(7):1035-1038.
APA 武文琼,丁昌华,&侯雪龙.(2012).Pd-Catalyzed Diastereo- and Enantioselective [3+2]-Cycloaddition Reaction of Vinyl Epoxide with Nitroalkenes.Synlett(7),1035-1038.
MLA 武文琼,et al."Pd-Catalyzed Diastereo- and Enantioselective [3+2]-Cycloaddition Reaction of Vinyl Epoxide with Nitroalkenes".Synlett .7(2012):1035-1038.

入库方式: OAI收割

来源:上海有机化学研究所

浏览0
下载0
收藏0
其他版本

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。