Heparan sulfate (HS) and dermatan sulfate (DS) are l-iduronic
acid containing glycosaminoglycans (GAGs) which are implicated in
a number of biological processes and conditions including cancer and
viral infection. Chemical synthesis of HS and DS is required to generate
structurally defined oligosaccharides for a biological study. Herein,
we present a new synthetic approach to HS and DS oligosaccharides
using chemoselective glycosylation which relies on a disarmed [2.2.2] l-ido lactone motif. The strategy provides a general approach
for iterative-reducing end chain extension, using only shelf-stable
thioglycoside building blocks, exploiting a conformational switch
to control reactivity, and thus requires no anomeric manipulation
steps between glycosylations.