Difluoromethylene Phosphabetaine as an Equivalent of Difluoromethyl Carbanion
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文摘
A method for nucleophilic difluoromethylation of reactive Michael acceptors, aldehydes, and azomethines is described. The reaction is performed using the readily available and air-stable reagent difluoromethylene phosphabetaine. The process involves interaction of an electrophilic substrate with in situ generated difluorinated phosphonium ylide followed by hydrolysis of the carbon鈥損hosphorus bond under mild conditions.

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