Premium
Attempted Synthesis of Type‐A Inositolphosphoglycan Mediators – Synthesis of a Pseudohexasaccharide Precursor
Author(s) -
MartínLomas Manuel,
FloresMosquera María,
Chiara Joséluis
Publication year - 2000
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/(sici)1099-0690(200004)2000:8<1547::aid-ejoc1547>3.0.co;2-c
Subject(s) - chemistry , glycosylation , regioselectivity , acylation , glycosyl , stereochemistry , anomer , glycosidic bond , glycosyl donor , disaccharide , combinatorial chemistry , organic chemistry , catalysis , biochemistry , enzyme
A block synthesis approach to the inositol‐containing pseudohexasaccharide 1 is presented. The myo ‐inositol building block 6 has been prepared using a key regioselective acylation through a boron‐tin exchange reaction and the 2‐azido‐2‐deoxy glycosyl donors 15 and 17 have been synthesized from D ‐glucosamine using a diazo transfer reaction. The anomeric position of the mono‐ and disaccharide building blocks has been temporarily protected as phenyl thioglycoside and this function was then converted into the different leaving groups to perform the glycosylation reactions. Both trichloroacetimidates and fluorides have been used as glycosyl donors for the construction of the different glycosidic linkages. The protected pseudohexasaccharides 44 , 48‐50 , which are precursors of pseudohexasaccharide 1 , have been efficiently prepared and fully characterized. Pseudohexasaccharide 1 contains the fundamental structural features which have been proposed for type A inositolphosphoglycans, which may be involved in the insulin‐signaling process.