Abstract
The synthesis of phosphonic acid analogues of L-α-(distearoyl)cephalin and L-α-(dimyristoyl)cephalin is described. They were obtained by phosphonylating D-α,β-distearin and D-α,β-dimyristin with 2-phthalimidoethylphosphonic acid monochloride and triethylamine, and removing the protective phthaloyl group of distearoyl and dimyristoyl L-α-glyceryl-(2-phthalimidoethyl)phosphonate by hydrazinolysis.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
