Issue 22, 2021

N-Heterocyclic carbene-catalyzed [3 + 3] annulation of bromoenals with 2-aminochromones to access chromeno[2,3-b]pyridinones

Abstract

N-Heterocyclic carbene-catalyzed [3 + 3] annulation of bromoenals with 2-aminochromones has been successfully developed. A structurally diverse set of chromeno[2,3-b]pyridinones was efficiently constructed in acceptable to excellent yields. The reaction features mild reaction conditions, a broad substrate scope, and easy scale-up.

Graphical abstract: N-Heterocyclic carbene-catalyzed [3 + 3] annulation of bromoenals with 2-aminochromones to access chromeno[2,3-b]pyridinones

Supplementary files

Article information

Article type
Communication
Submitted
13 Apr 2021
Accepted
07 May 2021
First published
07 May 2021

Org. Biomol. Chem., 2021,19, 4882-4886

N-Heterocyclic carbene-catalyzed [3 + 3] annulation of bromoenals with 2-aminochromones to access chromeno[2,3-b]pyridinones

P. Jiang, J. Guo, M. Gong, X. Zhou, W. Cao, Z. Fu and W. Huang, Org. Biomol. Chem., 2021, 19, 4882 DOI: 10.1039/D1OB00720C

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