In this paper, an easy-operational, high-yielding method for the gram-scale synthesis of 3-sulfonyl flavanones is described by a one-pot straightforward POCl mediated intermolecular (5 + 1) annulation of the β-ketosulfones with an -hydroxyaryl group (dual nucleophile) and arylaldehydes (dual electrophile) in refluxing toluene for 3 h. A plausible mechanism is proposed and discussed. This protocol provides a highly effective annulation via one carbon-oxygen (C-O) and one carbon-carbon (C-C) bond formations.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.joc.9b02980 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!