674789-16-3Relevant articles and documents
Synthesis of new α or γ-functionalized hydroxymethylphosphinic acid derivatives
Cristau, Henri-Jean,Hervé, Agnès,Virieux, David
, p. 877 - 884 (2004)
The syntheses of new γ-ethoxycarbonyl- and α-amino-alkyl hydroxymethylphosphinic acid derivatives are described. These compounds were conveniently prepared by Michael addition or Kabachnik-Fields reaction of an original precursor, ethyl benzyloxymethyl hydrogenophosphinate, respectively to α,β-unsaturated esters using a basic activation or to imines. Selective deprotection of the alcohol function was achieved by hydrogenolysis on Pd/C, whereas lithium bromide was used to selectively cleave the phosphinate ester group. Acidic hydrolysis readily gave the free hydroxymethylphosphinic acids.
Synthesis of New Arylhydroxymethylphosphinic Acids and Derivatives
Cristau,Herve,Loiseau,Virieux
, p. 2216 - 2220 (2007/10/03)
The synthesis of a new series of arylhydroxymethylphosphinic acid derivatives is described. The protected compounds were prepared by a palladium(0) catalysed arylation of ethyl benzyloxymethylphosphinate with aryl halides. Subsequent hydrogenolysis of the
