Journal
CHEMICAL COMMUNICATIONS
Volume 56, Issue 8, Pages 1183-1186Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc08713c
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Funding
- National Natural Science Foundation of China [U1504205, 21303264]
- Key Research Project of Education Department of Henan Province [17A150002]
- Henan University [yqpy20170009]
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An effective annulation of ynones and (iso)quinoline N-oxides was developed to deliver various functionalized 3-((iso)quinolin-1-yl)-4H-chromen-4-ones and 13H-isoquinolino[2,1-a]quinolin-13-ones in moderate to excellent yields, respectively. This protocol exhibits high regioselectivity and broad substrate scope under transitionmetal-free conditions. Moreover, the key reaction intermediate was successfully isolated and determined unambiguously by single crystal X-ray crystallography.
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