One
of the most important reaction in glycochemistry
is certainly the glycosylation step during which
the link between two saccharides is created. The
stereoselectivity of this reaction can be controlled
by different protective groups in 2 position.
As
many polysaccharides possess a sulfate group in
this position, the influence of a nearby organosulfate
on the orientation of the glycosylation needed
to be investigated
In
this study, diverse derivatives (scheme) were synthesized
and tested.
To
learn more : web
page of the group
Supervisor : Dr. Reynald
CHEVALLIER
Director of the
Lab : Pr. Pierre SINAY
Address
: Ecole Normale Supérieure,
24
rue Lhomond, 75005 PARIS, FRANCE
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