中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A highly enantioselective organocatalyst for the michael addition of cyclic ketones to nitroolefins

文献类型:期刊论文

作者Zhu, MK; Cun, LF; Mi, AQ; Jiang, YZ; Gong, LZ
刊名Tetrahedron-asymmetry
出版日期2006-02-20
卷号17期号:4页码:491-493
ISSN号0957-4166
DOI10.1016/j.tetasy.2006.01.034
通讯作者Gong, lz(gonglz@cioc.ac.cn)
英文摘要Enantiomerically pure triamine 2, which catalyses the michael addition of cyclic ketones to nitroolefins with high diastereoselectivity (lip to 99:1) and enantioselectivity (lip to 91% ee), was designed and prepared. (c) 2006 published by elsevier ltd.
WOS关键词BIFUNCTIONAL ORGANOCATALYSTS ; ALDOL REACTIONS ; NITRO-OLEFINS ; ALDEHYDES ; NITROALKENES ; DERIVATIVES ; NITROSTYRENES ; CATALYSTS ; THIOUREA ; DIAMINE
WOS研究方向Chemistry
WOS类目Chemistry, Inorganic & Nuclear ; Chemistry, Organic ; Chemistry, Physical
语种英语
WOS记录号WOS:000236814300004
出版者PERGAMON-ELSEVIER SCIENCE LTD
URI标识http://www.irgrid.ac.cn/handle/1471x/2379889
专题中国科学院大学
通讯作者Gong, LZ
作者单位1.Chinese Acad Sci, Chengdu Inst Organ Chem, Key Lab Asymmetr Synth & Chirotechnol Sichuan Pro, Chengdu 610041, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
推荐引用方式
GB/T 7714
Zhu, MK,Cun, LF,Mi, AQ,et al. A highly enantioselective organocatalyst for the michael addition of cyclic ketones to nitroolefins[J]. Tetrahedron-asymmetry,2006,17(4):491-493.
APA Zhu, MK,Cun, LF,Mi, AQ,Jiang, YZ,&Gong, LZ.(2006).A highly enantioselective organocatalyst for the michael addition of cyclic ketones to nitroolefins.Tetrahedron-asymmetry,17(4),491-493.
MLA Zhu, MK,et al."A highly enantioselective organocatalyst for the michael addition of cyclic ketones to nitroolefins".Tetrahedron-asymmetry 17.4(2006):491-493.

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来源:中国科学院大学

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