919081-71-3

Upstream product

• 849619-43-8 1,6-anhydro-4-O-benzyl-2-O-[(R)-α-(ethoxycarbonyl)benzyl]-β-D-glucopyranose 
• 2937-50-0 Allyl chloroformate 
• 10606-72-1 (R)-mandelic acid ethyl ester 
• 33208-47-8 4-O-benzyl-1,6:2,3-dianhydro-β-D-mannopyranose 

Downstream Products

• 919081-73-5 1,6-di-O-acetyl-3-O-allyloxycarbonyl-4-O-benzyl-2-O-[(R)-ethoxycarbonylbenzyl]-α-D-glucopyranose 
• 919081-76-8 6-O-acetyl-3-O-allyloxycarbonyl-4-O-benzyl-2-O-[(R)-ethoxycarbonylbenzyl]-α-D-glucopyranosyl trichloroacetimidate 
• 919081-78-0 1,6-anhydro-3-O-allyl-4-O-benzyl-2-O-[(R)-ethoxycarbonylbenzyl]-β-D-glucopyranose 

Relevant academic research and scientific papers

Stereoselective glycosylations using (R)- or (S)-(ethoxycarbonyl)benzyl chiral auxiliaries at C-2 of glycopyranosyl donors

The stereoselective introduction of a glycosidic bond presents the greatest challenge to complex oligosaccharide synthesis. Important developments such as automated polymer-supported oligosaccharide synthesis will not realize their full potential until th