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Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to alpha,beta-Unsaturated Aldehydes by Redox Oxidation
文献类型：期刊论文
| 作者 | Rong ZQ(荣子强) ; Jia MQ(贾敏强) ; You SL(游书力) |
| 刊名 | Org. Lett.
 |
| 出版日期 | 2011 |
| 卷号 | 13期号:15页码:4080-4083 |
| ISSN号 | 1523-7060 |
| 其他题名 | 氮杂环卡宾催化的对α,β-不饱和醛的不对称氧化Michael加成 |
| 通讯作者 | 游书力 |
| 英文摘要 | Enantioselective N-heterocyclic carbene-catalyzed Michael addition reactions to alpha,beta-unsaturated aldehydes by redox oxidation were realized. With 10 mol % of camphor-derived triazolium salt D, 15 mol % of DBU, 5 mol % of NaBF(4), and 100 mol % of quinone oxidant, the reactions of various dicarbonyl compounds with alpha,beta-unsaturated aldehydes led to 3,4-dihydro-alpha-pyrones in good yields and excellent ee's. |
| 学科主题 | 金属有机化学 |
| 收录类别 | SCI |
| 原文出处 | http://dx.doi.org/10.1021/ol201595f |
| 语种 | 英语 |
| WOS记录号 | WOS:000293252800079 |
| 公开日期 | 2013-03-04 |
| 源URL | [http://202.127.28.38/handle/331003/22542]  |
| 专题 | 上海有机化学研究所_金属有机化学国家重点实验室 |
| 推荐引用方式 GB/T 7714 | Rong ZQ,Jia MQ,You SL. Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to alpha,beta-Unsaturated Aldehydes by Redox Oxidation[J]. Org. Lett.,2011,13(15):4080-4083. |
| APA | 荣子强,贾敏强,&游书力.(2011).Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to alpha,beta-Unsaturated Aldehydes by Redox Oxidation.Org. Lett.,13(15),4080-4083. |
| MLA | 荣子强,et al."Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to alpha,beta-Unsaturated Aldehydes by Redox Oxidation".Org. Lett. 13.15(2011):4080-4083. |
入库方式： OAI收割
来源：上海有机化学研究所
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