37111-84-5

Upstream product

• 100-39-0 benzyl bromide 
• 127753-57-5 allyl-3-O-allyl-4,6-O-benzylidene-D-glucopyranoside 

Downstream Products

• 72984-63-5 1,3,4,6-tetra-O-acetyl-2-O-benzyl-α- and β-D-glucopyranose 
• 127753-62-2 (E)buta-1,3-dienyl 2-O-benzyl-3,4,6-tri-O-acetyl-α-D-glucopyranoside 
• 127753-61-1 (E)buta-1,3-dienyl 2-O-benzyl-3,4,6-tri-O-acetyl-β-D-glucopyranoside 
• 127753-64-4 (2R,3S,4S,5R,6S)-5-Benzyloxy-6-[((E)-buta-1,3-dienyl)oxy]-2-hydroxymethyl-tetrahydro-pyran-3,4-diol 
• 127753-63-3 (2R,3S,4S,5R,6R)-5-Benzyloxy-6-[((E)-buta-1,3-dienyl)oxy]-2-hydroxymethyl-tetrahydro-pyran-3,4-diol 
• 106680-71-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-(2-hydroxymethyl-2-methyl-cyclohexyloxy)-tetrahydro-pyran-3,4,5-triol 
• 127753-60-0 (E)(prop-2-enal)-3-yl 2-O-benzyl-3,4,6-tri-O-acetyl-β-D-glucopyranoside 
• 58719-77-0 2-O-benzyl-D-glucopyranose 
• 29741-69-3 3,4,6-tetra-O-acetyl-2-O-benzyl-α-D-glucopyranosyl bromide 

Relevant academic research and scientific papers

STEREOCHEMICAL VARIATIONS IN AQUEOUS CYCLOADDITIONS USING GLYCO-ORGANIC SUBSTRATES AS A CONSEQUENCE OF CHEMICAL MANIPULATIONS ON THE SUGAR MOIETY

Chemical modifications of the sugar moiety in dienyl glycosides allowed us to rationalize the stereochemistry of our aqueous cycloadditions using glyco-organic substrates.In this way, several dienyl glucosides having benzyl group in 2 or 6 position of the