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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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