Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 80, Issue 1, Pages 296-303Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo502362k
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- CSIR, India [P81102]
- CSIR-India
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A number of pharmaceutical compounds possess an arylated 2-pyridone moiety. The existing reports using expensive starting materials and/or superstoichiometric metal salts have prompted us to explore a possible user-friendly method for their synthesis. In this report, we demonstrate an easy-to-handle reaction condition with an iron catalyst for the exclusive generation of C-3-arylated pyridone via C-H functionalization.
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