Parasite glycoconjugates. Part 9. Synthesis of dec-9-enyl beta-D-galactopyranosyl-(1 -> 4)-alpha-D-mannopyranosyl phosphate and its epimers at the D-galactose moiety, substrate analogues for the elongating alpha-D-mannopyranosylphosphate transferase in the Leishmania
Ia. Ivanova et al., Parasite glycoconjugates. Part 9. Synthesis of dec-9-enyl beta-D-galactopyranosyl-(1 -> 4)-alpha-D-mannopyranosyl phosphate and its epimers at the D-galactose moiety, substrate analogues for the elongating alpha-D-mannopyranosylphosphate transferase in the Leishmania, J CHEM S P1, (12), 1999, pp. 1743-1753
A set of phosphodisaccharides, substrate analogues, which will be used to s
tudy the acceptor substrate specificity of the Leishmania biosynthetic enzy
mes, have been synthesized using the trichloroacetimidate method for the gl
ycosylation reactions, S(N)2 nucleophilic displacement of triflic esters fo
r epimerization and the glycosyl hydrogenphosphonate method for phosphoryla
tion.