A Highly Regioselective Palladium-Catalyzed Hydrophosphination of Alkynes Using a Diphosphine−Hydrosilane Binary System
摘要:
A novel transition-metal-catalyzed hydrophosphination of terminal alkynes using a diphosphine-hydrosilane binary system takes place regioselectively to provide vinylic phosphines, which undergo air oxidation during workup, affording the corresponding vinylphosphine oxides in good yields. In this hydrophosphination, hydrosilanes act as a useful hydrogen source, and furthermore, small amounts of oxygen is required to accomplish the reaction efficiently.
A novel rhodium(I)-catalyzed hydrophosphination of terminalalkynes with diphosphines and hydrosilanes takes place regioselectively in the presence of small amounts of oxygen. After air-oxidation during workups, the corresponding anti-Markovnikov–type vinylic phosphine oxides were obtained in good yields.