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Abstract
Abstract The in situ silylation of phosphorous acid diesters to phosphorous acid triesters by hexamethyldisilazane and trimethylsilyl halides under conditions of Michaelis-Arbuzov reaction was found as an efficient and facile reaction principle for P-C bond formation. In general the method can be applied also to Michaelis-Arbuzov reactions of phosphonous and hypophosphorous acid esters, to Tavs reaction of phosphorous and phosphonous acid esters as well as to photochemical conversions of arylhalides with trimethylsilyl phosphites. In any case described the observed yield is nearly quantitative.
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