Transition-metal-free insertion reactions of alkynes into the C-N σ-bonds of imides: synthesis of substituted enamides or chromones

A transition-metal-free tandem process for the synthesis of substituted enamides and chromones is presented. The insertion of isolated alkynes into the C-N σ-bonds of imides is involved in this tandem process. In the case of alkynones bearing an ortho -bromo-substituted aryl ring, chromones were selectively formed via the O -cyclization pathway. A variety of substituted enamides and chromones were prepared in good to high yields. Transition-metal-free insertion of ynones into the C-N σ-bonds of imides for the chemo-selective synthesis of chromones or enamides.