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One-Pot Synthesis of Heterocyclic Chromones by d is a document available to read on EtoBox.

This document describes the efficient one-pot synthesis of chromone and flavonoid derivatives bearing heterocyclic units. The reaction involves a Michael aldol reaction of chromone or flavonoid derivatives with pyridine-containing aldehydes. This allows the synthesis of 2,3-heterocyclic substituted chromones and flavonoids in one step. The reaction conditions were optimized and different pyridine aldehydes were examined. Some compounds showed cytotoxicity against cancer cells, demonstrating the potential fo

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d
Language
EN