PARASITE GLYCOCONJUGATES .1. THE SYNTHESIS OF SOME EARLY AND RELATED INTERMEDIATES IN THE BIOSYNTHETIC-PATHWAY OF GLYCOSYL-PHOSPHATIDYLINOSITOL MEMBRANE ANCHORS
S. Cottaz et al., PARASITE GLYCOCONJUGATES .1. THE SYNTHESIS OF SOME EARLY AND RELATED INTERMEDIATES IN THE BIOSYNTHETIC-PATHWAY OF GLYCOSYL-PHOSPHATIDYLINOSITOL MEMBRANE ANCHORS, Journal of the Chemical Society. Perkin transactions. I, (23), 1993, pp. 2945-2951
The enantio-pure 1D- and 1L-MYO-inositol derivatives 3D and 3L have be
en used to prepare sodium 1 amino-2-deoxy-alpha-D-glucopyranosyl)-myo-
inositol sn-2,3-dipalmitoyloxypropyl phosphate 21 and a related 1,6-di
substituted 1 L-MYO-inositol 28, respectively. The hydrogenphosphonate
approach was effective in coupling together the phosphonolipid moiety
16 and the protected zido-2-deoxy-alpha-D-glucopyranosyl)-myo-inosito
ls 15 and 24, respectively.