Bifunctional catalysis of Morita-Baylis-Hillman (MBH) reaction with chiral primary-tertiary diamine: A non-typical MBH catalytic pathway
文献类型：期刊论文
| 作者 | Zhang Long3,4; Luo SanZhong1,2; Chen LiuJuan1,2; Li JiuYuan1,2; Cheng JinPei3,4 |
| 刊名 | SCIENCE IN CHINA SERIES B-CHEMISTRY
 |
| 出版日期 | 2009-09-01 |
| 卷号 | 52期号:9页码:1300-1308 |
| 关键词 | Morita-baylis-hillman Reaction Primary Amine Enamine Iminium Organocatalyst |
| ISSN号 | 1006-9291 |
| DOI | 10.1007/s11426-009-0180-2 |
| 英文摘要 | A simple primary-tertiary diamine has been explored as a novel catalyst for the Morita-Baylis- Hillman reaction of MVK and aryl aldehydes, and moderate to good chemical yields were obtained. Detailed mechanism study indicated that the diamine acted as a bifunctional cooperation catalyst via a bicyclic enamino-quaternary ammonium intermediate. |
| 语种 | 英语 |
| WOS记录号 | WOS:000270191100003 |
| 出版者 | SCIENCE PRESS |
| 源URL | [http://ir.iccas.ac.cn/handle/121111/68141]  |
| 专题 | 中国科学院化学研究所 |
| 通讯作者 | Luo SanZhong |
| 作者单位 | 1.Chinese Acad Sci, Inst Chem, BNLMS, Beijing 100190, Peoples R China 2.Chinese Acad Sci, Inst Chem, Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China 3.Nankai Univ, Dept Chem, Tianjin 300071, Peoples R China 4.Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China |
| 推荐引用方式 GB/T 7714 | Zhang Long,Luo SanZhong,Chen LiuJuan,et al. Bifunctional catalysis of Morita-Baylis-Hillman (MBH) reaction with chiral primary-tertiary diamine: A non-typical MBH catalytic pathway[J]. SCIENCE IN CHINA SERIES B-CHEMISTRY,2009,52(9):1300-1308. |
| APA | Zhang Long,Luo SanZhong,Chen LiuJuan,Li JiuYuan,&Cheng JinPei.(2009).Bifunctional catalysis of Morita-Baylis-Hillman (MBH) reaction with chiral primary-tertiary diamine: A non-typical MBH catalytic pathway.SCIENCE IN CHINA SERIES B-CHEMISTRY,52(9),1300-1308. |
| MLA | Zhang Long,et al."Bifunctional catalysis of Morita-Baylis-Hillman (MBH) reaction with chiral primary-tertiary diamine: A non-typical MBH catalytic pathway".SCIENCE IN CHINA SERIES B-CHEMISTRY 52.9(2009):1300-1308. |
入库方式： OAI收割
来源：化学研究所
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