80153-00-0

Upstream product

• 80152-99-4 1-O-acetyl-2,3,4-tri-O-benzyl-6-deoxy-α-L-mannose 
• 100-51-6 benzyl alcohol 
• 80161-75-7 Benzyl-2,3,4-tri-O-benzyl-β-L-rhamnopyranosid 
• 210426-02-1 2,3,4-tri-O-benzyl-L-rhamnopyranose 

Downstream Products

• 210426-02-1 2,3,4-tri-O-benzyl-L-rhamnopyranose 

Relevant academic research and scientific papers

Facile glycosylation strategy with two-stage activation of allyl glycosyl donors. Application to concise synthesis of Shigella flexneri serotype y O-antigen

A practical, useful glycosylation method employing only allyl glycoside building blocks has been developed. The donor's glycosylation reactivity is turned on via isomerization of its anomeric allyl protecting group into the corresponding prop-1-enyl moiet

Building Units for Oligosaccharides, XXXIII. Synthesis of β-Glycosidically Linked Disaccharides of L-Rhamnose

The 2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl bromide (4) is a reactive halogenose which in the presence of a silver silicate catalyst reacts with saccharides containing a reactive hydroxyl group to give a β-glycosidically linked disaccharide with good selec