140420-59-3

Upstream product

• 140420-56-0 allyl 2,4-di-O-benzyl-α-D-xylopyranoside 
• 1253793-29-1 C₂₉H₃₂O₅ 
• 140420-69-5 allyl α-D-xylopyranoside 
• 100-39-0 benzyl bromide 
• 95898-05-8 2,3,4-tri-O-benzyl-α-D-xylopyranosyl fluoride 

Downstream Products

• 140420-60-6 1-propenyl O-(2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1-3)-2,4-di-O-benzyl-α-D-xylopyranoside 
• 140420-58-2 1-propenyl O-(2,3,4-tri-O-benzyl-α-D-xylopyranosyl)-(1-3)-2,4-di-O-benzyl-α-D-xylopyranoside 
• 140420-62-8 O-(2,3,4-tri-O-benzyl-α-D-xylopyranosyl)-(1-3)-2,4-di-O-benzyl-β-D-xylopyranosyl fluoride 
• 140664-95-5 O-(2,3,4-tri-O-benzyl-α-D-xylopyranosyl)-(1-3)-2,4-di-O-benzyl-α-D-xylopyranosyl fluoride 

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

Simple glycosylation reaction of allyl glycosides

(Chemical Equation Presented) A simple glycosylation strategy employing only allyl glycosides is described. In a one-pot fashion, an allyl glycoside is first isomerized to the reactive 1-prop-en-yl glycoside intermediate, which subsequently undergoes glyc

Stereoselective α-glycosylation with 3-O-acetylated D-gluco donors

The effect of a 3-O-acetyl group on the stereoselectivity of α-glycosylation with 2-O-benzylated D-gluco glycosyl donors was studied. It was shown that 3-O-acetylated donors gave α-anomers predominantly or exclusively, whereas glycosylation with the corre