期刊
CANADIAN JOURNAL OF CHEMISTRY
卷 96, 期 12, 页码 1071-1078出版社
CANADIAN SCIENCE PUBLISHING, NRC RESEARCH PRESS
DOI: 10.1139/cjc-2017-0564
关键词
multicomponent reaction; dimedone-based enaminones; tetrahydrobiquinoline-2,5-(1H,3H)-diones; DFT; computational
资金
- Alzahra University Research Council
- Iran Science National Foundation (INSF)
A novel series of N-functionalized 4-aryl-tetrahydrobiquinoline-2,5-(1H,3H)-diones were synthesized in high yields by a one-pot three-component reaction involving 2-chloroquinoline-3-carbaldehydes, Meldrum's acid, and enaminones (dimedone-based enaminones) in the presence of K(2)CO(3 )in CH3CN under reflux condition. To gain a deep insight on the mechanism of the reaction, an extensive series of quantum mechanics calculations in the framework of density functional theory (DFT) were carried out for supporting the suggested reaction pathway.
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