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L-Proline derived triamine as a highly stereoselective organocatalyst for asymmetric Michael addition of cyclohexanone to nitroolefins
文献类型：期刊论文
| 作者 | Chen, HB; Wang, Y; Wei, SY; Sun, J; Sun, J, Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China. |
| 刊名 | TETRAHEDRON-ASYMMETRY
 |
| 出版日期 | 2007 |
| 卷号 | 18期号:11页码:1308_1312 |
| ISSN号 | 0957-4166 |
| 产权排序 | 1 |
| 英文摘要 | L-Proline derived triamine 4 has been developed as a highly efficient and stereoselective organocatalyst for the asymmetric Michael addition of cyclohexanone to nitroolefins. In the presence of (CF3SO2)(2)NH, 4 catalyzed the reaction of cyclohexanone to a variety of nitroolefins with high yields (up to 99%) and excellent diastereoselectivities (up to 99:1 dr) and enantioselectivities (up to 98% ee). (c) 2007 Elsevier Ltd. All rights reserved. |
| 学科主题 | Chemistry, Inorganic & Nuclear ; Chemistry, Organic ; Chemistry, Physical |
| 语种 | 英语 |
| WOS记录号 | WOS:000248633100008 |
| 公开日期 | 2011-07-08 |
| 源URL | [http://210.75.237.14/handle/351003/17947]  |
| 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 | Chen, HB,Wang, Y,Wei, SY,et al. L-Proline derived triamine as a highly stereoselective organocatalyst for asymmetric Michael addition of cyclohexanone to nitroolefins[J]. TETRAHEDRON-ASYMMETRY,2007,18(11):1308_1312. |
| APA | Chen, HB,Wang, Y,Wei, SY,Sun, J,&Sun, J, Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China..(2007).L-Proline derived triamine as a highly stereoselective organocatalyst for asymmetric Michael addition of cyclohexanone to nitroolefins.TETRAHEDRON-ASYMMETRY,18(11),1308_1312. |
| MLA | Chen, HB,et al."L-Proline derived triamine as a highly stereoselective organocatalyst for asymmetric Michael addition of cyclohexanone to nitroolefins".TETRAHEDRON-ASYMMETRY 18.11(2007):1308_1312. |
入库方式： OAI收割
来源：成都生物研究所
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