Issue 38, 2024

Iridium-catalyzed asymmetric cascade dearomative allylation/acyl transfer rearrangement: access to chiral N-substituted 2-pyridones

Abstract

Iridium-catalyzed dearomative allylation/acyl transfer rearrangement has been developed using easily available 2-pyridinyl benzoates and vinyl ethylene carbonate. This protocol enabled the expedient synthesis of a variety of chiral N-substituted 2-pyridones in good to high yields with excellent enantioselectivity. It has the advantages of high atom economy, wide substrate scope, gram-scale synthesis, and versatile synthetic transformations.

Graphical abstract: Iridium-catalyzed asymmetric cascade dearomative allylation/acyl transfer rearrangement: access to chiral N-substituted 2-pyridones

Supplementary files

Article information

Article type
Communication
Submitted
28 Feb 2024
Accepted
05 Apr 2024
First published
08 Apr 2024

Chem. Commun., 2024,60, 5086-5089

Iridium-catalyzed asymmetric cascade dearomative allylation/acyl transfer rearrangement: access to chiral N-substituted 2-pyridones

W. Wang, Z. Yi, Z. Wang, X. Dong and C. Wang, Chem. Commun., 2024, 60, 5086 DOI: 10.1039/D4CC00944D

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