文摘
Highly regio- and stereoselective hydrosilylation applicable to a broad range of electron-deficient alkynes has been established using palladium catalysis. The synthetic utility of the method has been demonstrated by further transformations of 伪-silylalkenes, particularly Hiyama coupling and stereoinverting iododesilylation followed by Suzuki鈥揗iyaura coupling, which enables stereodivergent syntheses of 伪-arylenoates.