Oligosaccharide Synthesis via Electrophile-Induced Activation of Glycosyl-N-Allylcarbamates
Holger Herzner, Jörg Eberling, Michael K. Schultz, Jörg Zimmer, Horst Kunz
Abstract
Holger Herzner, Jörg Eberling, Michael K. Schultz, Jörg Zimmer, Horst Kunz
Abstract
Glycosyl-N-allyl carbamates, obtained by reaction of anomerically unprotected saccharides with allyl isocyanate, can be activated by an electrophile-induced cyclisation and reacted with glycosyl acceptors to form the corresponding oligosaccharides By this method the mucin core 2 trisaccharide2 has successfully been synthesized. Due to the mild glycosylation conditions even 1-O-acetyl protected glycosyl acceptors can be used. This was demonstrated in the synthesis of a 1,6-linked glucosyl trisaccharide whereby a reptitious glycosylation strategy could be applied. 1. Dedicated to the memory of Professor Akira Hasegawa.
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Glycosyl-N-allyl carbamates, obtained by reaction of anomerically unprotected saccharides with allyl isocyanate, can be activated by an electrophile-induced cyclisation and reacted with glycosyl acceptors to form the corresponding oligosaccharides By this method the mucin core 2 trisaccharide2 has successfully been synthesized. Due to the mild glycosylation conditions even 1-O-acetyl protected glycosyl acceptors can be used. This was demonstrated in the synthesis of a 1,6-linked glucosyl trisaccharide whereby a reptitious glycosylation strategy could be applied. 1. Dedicated to the memory of Professor Akira Hasegawa.
Key concepts: Chemistry, Glycosyl, Electrophile, Oligosaccharide, Glycan, Glycosyl donor, Stereochemistry, Biochemistry