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A three-component difunctionalization of N-alkenyl amides via organophotoredox radical-polar crossover.

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Herein, we report a three-component organophotoredox coupling of N-alkenyl amides with α-bromocarbonyls and various nucleophiles. This transition metal-free difunctionalization protocol installs sequential C-C and C-Y (Y = S/O/N) bonds in… Click to show full abstract

Herein, we report a three-component organophotoredox coupling of N-alkenyl amides with α-bromocarbonyls and various nucleophiles. This transition metal-free difunctionalization protocol installs sequential C-C and C-Y (Y = S/O/N) bonds in alkenes. This reaction works with terminal and internal alkenes containing both cyclic and acyclic amides via radical-polar crossover.

Keywords: amides via; difunctionalization; polar crossover; alkenyl amides; three component; radical polar

Journal Title: Chemical communications
Year Published: 2022

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