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N-Heterocyclic carbene-catalyzed 3 + 3 annulation of bromoenals with 2-aminochromones has been successfully developed. A structurally diverse set of chromeno2,3-bpyridinones was efficiently constructed in acceptable to excellent yields. The reaction features mild reaction conditions, a broad substrate scope, and easy scale-up.
Jiang et al. (Fri,) studied this question.
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