期刊
ADVANCED SYNTHESIS & CATALYSIS
卷 354, 期 13, 页码 2537-2544出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201200412
关键词
biaryls; 1; 3-; 1; 2-dicarbonyls; dual heterogeneous catalysis; multicomponent recations; pyridines
资金
- French Research Ministry for a fellowship award
- CNRS
- Conseil Regional PACA
- Aix-Marseille University
- CNRS [UMR 7313 iSm2, RDR2 research network]
- French Research Ministry
We have designed a new, user-friendly oxidative dual heterogeneous catalytic system capable of promoting polysubstituted pyridines as unique products from simple activated Michael acceptors, 1,3-dicarbonyls and ammonium acetate. This metal-free environmentally-respectful and totally regioselective domino reaction proved to be a great strategy to access bi- and triaryl-type pyridines as well as challenging bi- and triheteroaryl-type pyridines in a single operation.
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