Issue 6, 2021

Visible light-mediated cross-coupling of electrophiles: synthesis of α-amino amides from isocyanates and ketimines

Abstract

A catalytic system to synthesize α-amino amides from isocyanates and ketimines has been developed using visible light iridium photoredox catalysis via umpolung reactivity of ketimines. Cross-couplings between diverse ketimine and isocyanate substrates have been evaluated, affording the desired α-amino amide products in good yields. In addition, a metal-free catalytic system using perylene and N,N-diisopropylethylamine has been developed. Finally, single-step synthesis of the psychoactive drug benzodiazepine-2-one analogue from one of the coupling products has been achieved, indicating the great application potential of the synthetic method developed herein.

Graphical abstract: Visible light-mediated cross-coupling of electrophiles: synthesis of α-amino amides from isocyanates and ketimines

Supplementary files

Article information

Article type
Research Article
Submitted
23 Dec 2020
Accepted
15 Jan 2021
First published
18 Jan 2021

Org. Chem. Front., 2021,8, 1227-1232

Visible light-mediated cross-coupling of electrophiles: synthesis of α-amino amides from isocyanates and ketimines

J. Zhu, C. Dai, M. Ma, Y. Yue and X. Fan, Org. Chem. Front., 2021, 8, 1227 DOI: 10.1039/D0QO01620A

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