Selective photoredox decarboxylation of α-ketoacids to allylic ketones and 1,4-dicarbonyl compounds dependent on cobaloxime catalysis

A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The gener...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2020-10, Vol.56 (83), p.1253-12533
Hauptverfasser: Zhang, Hong, Xiao, Qian, Qi, Xu-Kuan, Gao, Xue-Wang, Tong, Qing-Xiao, Zhong, Jian-Ji
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Sprache:eng
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Zusammenfassung:A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The generality, good substrate scope and mild conditions are good features in the photoredox/cobaloxime catalysis protocol, and this method will provide new opportunities for the functionalization of more olefins. The selective synthesis of allylic ketones and 1,4-dicarbonyl compounds by photoredox/cobaloxime co-catalysis and photoredox catalysis, respectively, is described herein.
ISSN:1359-7345
1364-548X
DOI:10.1039/d0cc05580h