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N-Heterocyclic carbene-catalyzed [3 + 3] annulation of bromoenals with 2-aminochromones to access chromeno[2,3-b]pyridinones†
Pengrui Jiang,Jingcheng Guo,Minghua Gong,Xiangui Zhou,Wei Cao,Zhenqian Fu,Wei Huang
Organic & Biomolecular Chemistry Pub Date : 05/07/2021 00:00:00 , DOI:10.1039/D1OB00720C
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
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