Aryl-copper(III)-acetylides as key intermediates in Csp2-Csp model couplings under mild conditions.

The mechanism of copper-mediated Sonogashira couplings (so-called Stephens-Castro and Miura couplings) is not well understood and lacks clear comprehension. In this work, the reactivity of a well-defined aryl-Cu(III) species (1ClO4) with p-R-phenylacetylenes (R = NO2, CF3, H) is reported and it is found that facile reductive elimination from a putative aryl-Cu(III)-acetylide species occurs at room temperature to afford the Caryl-Csp coupling species (IR), which in turn undergo an intramolecular reorganisation to afford final heterocyclic products containing 2H-isoindole (P NO2, P CF3, PHa) or 1,2-dihydroisoquinoline (PHb) substructures. Density Functional Theory (DFT) studies support the postulated reductive elimination pathway that leads to the formation of C sp2-Csp bonds and provide the clue to understand the divergent intramolecular reorganisation when p-H-phenylacetylene is used. Mechanistic insights and the very mild experimental conditions to effect Caryl-Csp coupling in these model systems provide important insights for developing milder copper-catalysed Caryl-Csp coupling reactions with standard substrates in the future.