A team led by Yong-Qiang Tu (Lanzhou University, #China) has developed a highly enantioselective approach to synthesize α-ethynylated 3-substituted oxindoles using a hypervalent iodine alkynyl donor and a triazolium bromide catalyst. This method delivers excellent yields and enantioselectivity, providing key intermediates for alkaloid synthesis — demonstrated in their recent publication in Angewandte Chemie.