127753-67-7

Upstream product

• 100-39-0 benzyl bromide 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 
• 20675-63-2 6-O-benzyl-D-glucopyranose 
• 23397-86-6 6-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 109280-59-3 6-O-benzyl-1,2,3,4 tetra-O-acetyl D-glucopyranose 

Downstream Products

• 127753-69-9 (E)(prop-2-enal)3-yl 6-O-benzyl-3,4,5-tri-O-acetyl-β-D-glucopyranoside 
• 127753-70-2 (E)(prop-2-enal)3-yl 6-O-benzyl-3,4,5-tri-O-acetyl-α-D-glucopyranoside 
• 130034-84-3 6-O-Benzyl-2,3,4-tri-O-acetyl-α-D-glucopyranosyl chloride 
• 130034-82-1 (E)-4-(6'-O-Benzyl-2',3',4'-tri-O-acetyl-β-D-glucopyranosyloxy)but-3-en-2-one 
• 130034-80-9 (E)-4-(6'-O-Benzyl-2',3',4'-tri-O-acetyl-α-D-glucopyranosyloxy)but-3-en-2-one 
• 106680-71-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-(2-hydroxymethyl-2-methyl-cyclohexyloxy)-tetrahydro-pyran-3,4,5-triol 
• 127753-74-6 (2R,3S,4S,5R,6S)-2-Benzyloxymethyl-6-[((E)-buta-1,3-dienyl)oxy]-tetrahydro-pyran-3,4,5-triol 
• 127753-73-5 (2R,3S,4S,5R,6R)-2-Benzyloxymethyl-6-[((E)-buta-1,3-dienyl)oxy]-tetrahydro-pyran-3,4,5-triol 
• 127753-71-3 (E)buta-1,3-dienyl 6-O-benzyl-2,3,4-tri-O-acetyl-β-D-glucopyranoside 
• 127753-72-4 (E)buta-1,3-dienyl 6-O-benzyl-2,3,4-tri-O-acetyl-α-D-glucopyranoside 
• 132247-70-2 (1S,2S,3R)-5-oxo-N-phenyl-3-(2',3',4'-tri-O-acetyl-α-D-glucopyranosyloxy)cyclohexane-1,2-dicarboximide 
• 132247-70-2 (1R,2R,3S)-5-oxo-N-phenyl-3-(2',3',4'-tri-O-acetyl-β-D-glucopyranosyloxy)cyclohexane-1,2-dicarboximide 
• 130034-69-4 (E)-1-(6'-O-Benzyl-2',3',4'-tri-O-acetyl-α-D-glucopyranosyloxy)-3-(t-butyldimethylsiloxy)buta-1,3-diene 
• 130034-71-8 (E)-1-(6'-O-Benzyl-2',3',4'-tri-O-acetyl-β-D-glucopyranosyloxy)-3-(t-butyldimethylsiloxy)buta-1,3-diene 

Relevant academic research and scientific papers

Asymmetric Diels-Alder Reactions. Part 4. Influence of Anomeric Configuration and 2'- and 6'-O-Benzyl Substitution on the Diastereofacial Reactivity of (E)-3-(t-Butyldimethylsiloxy)-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyloxy)-buta-1,3-diene

The 1-(2',3',4',6'-tetra-O-acetyl-α-D-glucopyranosyloxy), 1-(6'-O-benzyl-2',3',4'-tri-O-acetyl-α-D-glucopyranosyloxy), 1-(2'-O-benzyl-3',4',6'-tri-O-acetyl-α-D-glucopyranosyloxy), 1-(6'-O-benzyl-2',3',4'-tri-O-acetyl-β-D-glucopyranosyloxy), and 1-(2'-O-be

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