中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances

文献类型:期刊论文

作者Wang, Zhouyu ; Wang, Chao ; Zhou, Li ; Sun, Jian
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
出版日期2013
卷号11期号:5页码:787-797
ISSN号1477-0520
产权排序2
通讯作者Wang, ZY (reprint author), Xihua Univ, Dept Pharmaceut Engn, Chengdu, Peoples R China ; Sun, Jian
英文摘要A series of N-formamides derived from pipecolinic acid have been synthesized and tested as Lewis base catalysts for the enantioselective reduction of N-aryl imines by trichlorosilane. Through the investigation of the structure-efficacy relationship between the side amide group and catalytic performance, several highly effective catalysts were discovered. In particular, arylamido-type catalyst 5i and non-arylamido-type catalyst 6c exhibited high reactivity and enantioselectivity, furnishing the reduction of a wide variety of N-aryl imines with high isolated yields (up to 98%) and ee values (up to 96%) under mild conditions. Moreover, these two catalysts complement each other in terms of their tolerances to nonaromatic ketimines and non-methyl ketimines.
学科主题Chemistry
收录类别SCI
语种英语
WOS记录号WOS:000312946200012
公开日期2014-11-21
源URL[http://210.75.237.14/handle/351003/24195]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Wang, Zhouyu,Wang, Chao,Zhou, Li,et al. L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2013,11(5):787-797.
APA Wang, Zhouyu,Wang, Chao,Zhou, Li,&Sun, Jian.(2013).L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances.ORGANIC & BIOMOLECULAR CHEMISTRY,11(5),787-797.
MLA Wang, Zhouyu,et al."L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances".ORGANIC & BIOMOLECULAR CHEMISTRY 11.5(2013):787-797.

入库方式: OAI收割

来源:成都生物研究所

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