Visible-Light-Driven α-Aminoalkyl Radical-Mediated C(sp 3 )-C(sp) Cross-Coupling of Iodoalkanes and Alkynyl Bromides.

We herein report a simple protocol for metal-free cross-coupling between unactivated alkyl iodides and terminal alkynyl bromides promoted by visible light. The salient features of this transformation are the utilization of an organic photocatalyst and commercially available tri-n-butylamine as a reductant. This protocol couples a variety of unactivated iodoalkanes containing different functional groups and with a variety of terminal alkynyl bromides under mild reaction conditions to afford the substituted alkynes in good yields.