Journal
CHEMICAL COMMUNICATIONS
Volume 55, Issue 92, Pages 13840-13843Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc07173c
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Funding
- National Natural Science Foundation of China [81773575, 81703329]
- Non-profit Central Research Institute of Chinese Academy of Medical Sciences [2019-RC-HL-008]
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A Cp*Co-III-catalyzed arene C-H bond amidation/annulation of benzamides was developed to afford quinazolinone derivatives in one-pot with high yields and broad substrate scope. This method could be applied to the synthesis of quinazolinone drugs and late-stage modification of natural products.
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