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S-chiral sulfinamides as highly enantioselective organocatalysts

文献类型:期刊论文

作者Pei, D; Wang, ZY; Wei, SY; Zhang, Y; Sun, J; Sun, J, Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China.
刊名ORGANIC LETTERS
出版日期2006
卷号8期号:25页码:5912_5915
ISSN号1523-7060
产权排序1
英文摘要Easily accessible chiral sulfinamide 2 has been developed as the first highly efficient and enantioselective organocatalyst relying solely on a chiral sulfur center for stereochemical induction. In the presence of 20 mol % of 2, a broad range of N-aryl ketimines 1 were reduced by trichlorosilane to produce amines 3 in high yield and enantioselectivity.
学科主题Chemistry, Organic
语种英语
WOS记录号WOS:000242405900059
公开日期2011-07-08
源URL[http://210.75.237.14/handle/351003/17829]  
专题成都生物研究所_天然产物研究
通讯作者Sun, J, Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China.
推荐引用方式
GB/T 7714
Pei, D,Wang, ZY,Wei, SY,et al. S-chiral sulfinamides as highly enantioselective organocatalysts[J]. ORGANIC LETTERS,2006,8(25):5912_5915.
APA Pei, D,Wang, ZY,Wei, SY,Zhang, Y,Sun, J,&Sun, J, Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China..(2006).S-chiral sulfinamides as highly enantioselective organocatalysts.ORGANIC LETTERS,8(25),5912_5915.
MLA Pei, D,et al."S-chiral sulfinamides as highly enantioselective organocatalysts".ORGANIC LETTERS 8.25(2006):5912_5915.

入库方式: OAI收割

来源:成都生物研究所

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