-promoted protocol for the selective and controllable esterification of P(O)OH compounds using O-nucleophiles (alcohols and phenols) as efficient esterification reagents is described. This method features a high efficiency and good functional-group tolerance, meaning a simple way to synthesize a broad spectrum of phosphinic and phosphoric acid esters from basic starting materials with moderate to excellent
Electrochemical Dehydrogenative Phosphorylation of Alcohols for the Synthesis of Organophosphinates
作者:Lingling Deng、Yang Wang、Haibo Mei、Yi Pan、Jianlin Han
DOI:10.1021/acs.joc.8b02882
日期:2019.1.18
An eco-friendly and efficient method for the synthesis of organophosphinates via an electrochemical cross-dehydrogenative-coupling reaction between alcohols and secondary phosphine oxides has been developed. This electrochemical reaction was conducted at room temperature without the addition of any oxidant, metal catalyst, or additive, which provides a new strategy for the synthesis of organophosphinates
Rapid and high yield oxidation of phosphine, phosphite and phosphinite compounds to phosphine oxides, phosphates and phosphinates using hypofluorous acid–acetonitrile complex
作者:Weimin Peng、Jean’ne M. Shreeve
DOI:10.1016/j.jfluchem.2005.02.012
日期:2005.7
The hypofluorousacid acetonitrile complex was used as a mild, rapid, and effective agent to oxidize a wide variety of phosphines, phosphites and phosphinites to the corresponding phosphine oxide, phosphate and phosphinate compounds.