trans-4-hydroxy-L-proline hydrazide-trifluoroacetic acid as highly stereoselective organocatalyst for the asymmetric direct aldol reaction of cyclohexanone
文献类型：期刊论文
| 作者 | Cheng, CL ; Wei, SY ; Sun, J |
| 刊名 | SYNLETT
 |
| 出版日期 | 2006 |
| 期号 | 15页码:2419_2422 |
| 关键词 | proline hydrazide enantioselectivity diastereoselectivity cyclohexanone asymmetric direct aldol reaction |
| ISSN号 | 0936-5214 |
| 产权排序 | 1 |
| 通讯作者 | Sun, J, Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China. |
| 中文摘要 | Protonated A,-benzyl-N '-L-prolyl-trans-4-hydroxy-L-proline hydrazide has been found to be superior to the L-proline hydrazide counterpart as the catalyst for the asymmetric aldol reaction of cyclohexanone and aromatic aldehydes, resulting in excellent diastereoselectivities (up to > 99:1 dr) and enantioselectivities (up to > 99% ee). |
| 学科主题 | Chemistry, Organic |
| 收录类别 | SCI |
| 语种 | 英语 |
| WOS记录号 | WOS:000241175500014 |
| 公开日期 | 2011-07-08 |
| 源URL | [http://210.75.237.14/handle/351003/17845]  |
| 专题 | 成都生物研究所_天然产物研究 |
| 推荐引用方式 GB/T 7714 | Cheng, CL,Wei, SY,Sun, J. trans-4-hydroxy-L-proline hydrazide-trifluoroacetic acid as highly stereoselective organocatalyst for the asymmetric direct aldol reaction of cyclohexanone[J]. SYNLETT,2006(15):2419_2422. |
| APA | Cheng, CL,Wei, SY,&Sun, J.(2006).trans-4-hydroxy-L-proline hydrazide-trifluoroacetic acid as highly stereoselective organocatalyst for the asymmetric direct aldol reaction of cyclohexanone.SYNLETT(15),2419_2422. |
| MLA | Cheng, CL,et al."trans-4-hydroxy-L-proline hydrazide-trifluoroacetic acid as highly stereoselective organocatalyst for the asymmetric direct aldol reaction of cyclohexanone".SYNLETT .15(2006):2419_2422. |
入库方式： OAI收割
来源：成都生物研究所
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