作者:Gnon Baba、Jean-François Pilard、Khalid Tantaoui、Annie-Claude Gaumont、Jean-Marc Denis
DOI:10.1016/0040-4039(95)00761-z
日期:1995.6
A general method for preparing secondary P-alkenyl and P-alkynyl phosphine oxides, compounds unknown so far, involves the condensation of the vinyl Grignard reagent or lithium acetylide on P-chloroaminophosphines followed by acidic hydrolysis of the corresponding vinyl- or ethynylaminophosphines on a solid acid (Amberlyst 15). The few reported chemical properties are mainly related to the strong PH bond activation. Of special interest is the addition of a secondary vinylphosphine oxyde derivative on methyl acrylate which occurs at room temperature without any catalyst.