Asymmetric α-Pentadienylation of ß-Ketocarbonyls and Aldehydes by Synergistic Pd/Chiral Primary Amine Catalysis

被引:3
|
作者
You, Chang [1 ]
Luo, Sanzhong [1 ]
机构
[1] Tsinghua Univ, Ctr Basic Mol Sci, Dept Chem, Beijing 100084, Peoples R China
关键词
alpha-Pentadienylation; Synergistic catalysis; Chiral primary amine; Pd catalysis; Hydrocarbons; ALLYLIC ALKYLATION; BETA-KETOCARBONYLS; DIENYL ACETATES; 1,3-DIENES; ACRYLATES; MECHANISM; ALKENES;
D O I
10.1002/cjoc.202300462
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Direct alkylation with skipped enynes or cyclopropropylacetylenes represents an ideal process for the installation of pentadienyl group in terms of atom- and step-economy. The development of catalytic asymmetric versions has been frequently pursued and most of the successes have been achieved with enolizable aldehydes. We herein describe a synergistic chiral primary amine/Pd catalysis for asymmetric a-pentadienylation of ss-ketocarbonyls and aldehydes with skipped enynes or cyclopropropylacetylenes. The reaction features the construction of acyclic all-carbon quaternary centers with high enantioselectivity, and good functional group tolerance and scalability.
引用
收藏
页码:3533 / 3538
页数:6
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