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Organic photoredox catalytic amino-heteroarylation of unactivated olefins to access distal amino ketones.

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Here we describe a metal-free amino-heteroarylation of unactivated olefins via organic photoredox catalysis, providing a concise and efficient approach for the rapid synthesis of various δ (β, ε)-amino ketones under… Click to show full abstract

Here we describe a metal-free amino-heteroarylation of unactivated olefins via organic photoredox catalysis, providing a concise and efficient approach for the rapid synthesis of various δ (β, ε)-amino ketones under mild conditions. This protocol demonstrates that the new photocatalyst Cz-NI developed by our group has an excellent photoredox catalytic performance. Finally, a series of mechanistic experiments and DFT calculations indicate that this transformation undergoes a photoredox catalytic sequential radical addition/functional group migration process.

Keywords: amino heteroarylation; organic photoredox; heteroarylation unactivated; photoredox catalytic; amino; unactivated olefins

Journal Title: Chemical communications
Year Published: 2022

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