Abstract
A palladium catalyzed synthesis of N-H phenanthridinones was developed via C-H arylation. The protocol gives phenanthridinones regioselectively by one-pot reaction without deprotection. It exhibits broad substrate scope and affords targets in up to 95% yields. Importantly, it could be applied for the less reactive o-chlorobenzamides.
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CITATION STYLE
APA
Hu, Q. F., Gao, T. T., Shi, Y. J., Lei, Q., & Yu, L. T. (2018). Palladium-catalyzed intramolecular C-H arylation of 2-halo-: N -Boc- N -arylbenzamides for the synthesis of N-H phenanthridinones. RSC Advances, 8(25), 13879–13890. https://doi.org/10.1039/c8ra02099j
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