Abstract
A procedure permitting the synthesis of both optical isomers as well as the racemic form of saturated or unsaturated phosphotidic acids is reported. The phosphotidic acids are obtainable by treating the pyridinium salts of L-, D-, or DL-dihydroxypropylphosphonic acid for 24 h at 80° with a mixture of the anhydride and the tetraethylammonium salt of the fatty acid to be introduced, and separating the reaction products by column chromatography on silicic acid. The preparation of the dipalmitoyl and distearoyl L-dihydroxypropylphosphonic acids is described.
Publisher
Canadian Science Publishing
Cited by
16 articles.
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