Abstract
C(sp3)–H bond functionalization is a powerful strategy for the synthesis of organic compounds due their abundance in simple starting materials. Photoredox catalysis has led to a diverse array of enabling C(sp3)–H activation strategies; however, the direct functionalization of C(sp3)–H to carboxylic acid derivatives remains underexplored. Disclosed herein is the development of a cooperative NHC/photoredox-catalyzed C(sp3)–H esterification transformation. This method enables access to benzylic, 𝛼–heteroatom, and formal β-esterification products in good to excellent yields under mild reaction conditions.



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