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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
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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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