Issue 27, 2024

Green light-mediated dual eosin Y/PdII-catalyzed C(sp2)–H arylation of N–H unprotected 2-arylquinazolinones

Abstract

We report herein an eosin Y/Pd(II) dual catalytic approach for regio- and chemoselective C(sp2)–H monoarylation of N–H unprotected 2-phenyl quinazolinone derivatives under green light irradiation with no necessity for any base/additive/external oxidant. The free N–H moiety was post-modified for quinazolinone scaffold diversification and C–H annulation.

Graphical abstract: Green light-mediated dual eosin Y/PdII-catalyzed C(sp2)–H arylation of N–H unprotected 2-arylquinazolinones

Supplementary files

Article information

Article type
Communication
Submitted
13 May 2024
Accepted
19 Jun 2024
First published
20 Jun 2024

Org. Biomol. Chem., 2024,22, 5540-5545

Green light-mediated dual eosin Y/PdII-catalyzed C(sp2)–H arylation of N–H unprotected 2-arylquinazolinones

S. Mondal and R. Jana, Org. Biomol. Chem., 2024, 22, 5540 DOI: 10.1039/D4OB00779D

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