Yoshida
et al. have reported that the novel three-component coupling using benzyne (prepared from
2-(trimethylsilyl)phenyl trifluoromethanesulfonate and KF), DMF and active methylene compounds provides direct access to coumarins. They have demonstrated that
ortho-quinone methide, arising from a formal [2+2] cycloaddition between benzyne and DMF, undergoes a [4+2] cycloaddition with ester enolates or ketenimine anions to produce coumarins, which are an important class of bioactive compounds.