中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective nickel-catalyzed alkylative alkyne-aldehyde cross-couplings

文献类型:期刊论文

作者Nie M(聂明); Fu WZ(付文振); Cao ZP(曹子平); Tang WJ(汤文军)
刊名Org. Chem. Front.
出版日期2015
卷号2期号:10页码:1322-1325
其他题名对映选择性镍催化烷基化炔醛偶联
通讯作者汤文军
英文摘要An efficient asymmetric nickel-catalyzed alkylative alkyne-aldehyde cross-coupling is developed by employing a P-chiral monophosphorus ligand BI-DIME, allowing rapid access to a series of chiral tetra-substituted olefinic allylic alcohols in high yields and good to excellent ees. The three-component reactions enjoy excellent regio- and enantioselectivities, and a broad substrate scope from readily available starting materials.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c5qo00148j
语种英语
WOS记录号WOS:000364450000004
源URL[http://ir.sioc.ac.cn/handle/331003/39666]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位中科院上海有机化学研究所, 生命有机化学国家重点实验室
推荐引用方式
GB/T 7714
Nie M,Fu WZ,Cao ZP,et al. Enantioselective nickel-catalyzed alkylative alkyne-aldehyde cross-couplings[J]. Org. Chem. Front.,2015,2(10):1322-1325.
APA 聂明,付文振,曹子平,&汤文军.(2015).Enantioselective nickel-catalyzed alkylative alkyne-aldehyde cross-couplings.Org. Chem. Front.,2(10),1322-1325.
MLA 聂明,et al."Enantioselective nickel-catalyzed alkylative alkyne-aldehyde cross-couplings".Org. Chem. Front. 2.10(2015):1322-1325.

入库方式: OAI收割

来源:上海有机化学研究所

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