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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.
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页码:3533 / 3538
页数:6
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