Issue 21, 1990

Synthesis of phospholipids using an inverse phosphite triester approach

Abstract

1,2-Diacylglycerols, prepared from allyl protected precursors, were transformed into glycerophosphatidylcholines through an acid catalysed coupling with a dialkyl phosphoramidite, followed by a one step deprotection–substitution reaction.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1497-1498

Synthesis of phospholipids using an inverse phosphite triester approach

N. Hébert and G. Just, J. Chem. Soc., Chem. Commun., 1990, 1497 DOI: 10.1039/C39900001497

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