23397-86-6

Upstream product

• 100-39-0 benzyl bromide 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 
• 32754-29-3 6-O-acetyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 22164-09-6 3,5-O-benzylidene-1,2-O-isopropylidene-α-D-glucofuranoside 
• 50-99-7 D-glucose 
• 15354-69-5 5,6-anhydro-1,2-O-isopropylidene-α-D-glucofuranose 
• 94265-83-5 O⁶-acetyl-O³,O⁵-((Ξ)-benzylidene)-O¹,O²-isopropylidene-α-D-glucofuranose 
• 50257-35-7 O⁶-benzyl-O³,O⁵-((Ξ)-benzylidene)-O¹,O²-isopropylidene-α-D-glucofuranose 

Downstream Products

• 101475-94-9 O⁶-benzyl-O³,O⁵-hydroxyphosphoryl-O¹,O²-isopropylidene-α-D-glucofuranose 
• 22170-16-7 O⁶-Benzyl-D-glucose 
• 33779-36-1 6-O-benzyl-1,2-O-isopropylidene-3,5-di-O-methyl-α-D-glucofuranose 
• 127753-70-2 (E)(prop-2-enal)3-yl 6-O-benzyl-3,4,5-tri-O-acetyl-α-D-glucopyranoside 
• 127753-69-9 (E)(prop-2-enal)3-yl 6-O-benzyl-3,4,5-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 
• 127753-71-3 (E)buta-1,3-dienyl 6-O-benzyl-2,3,4-tri-O-acetyl-β-D-glucopyranoside 
• 127753-73-5 (2R,3S,4S,5R,6R)-2-Benzyloxymethyl-6-[((E)-buta-1,3-dienyl)oxy]-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 
• 106680-71-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-(2-hydroxymethyl-2-methyl-cyclohexyloxy)-tetrahydro-pyran-3,4,5-triol 
• 127753-67-7 6-O-Benzyl-2,3,4-tri-O-acetyl-D-glucose 
• 109280-59-3 6-O-benzyl-1,2,3,4 tetra-O-acetyl D-glucopyranose 
• 20675-63-2 6-O-benzyl-D-glucopyranose 

Relevant academic research and scientific papers

Tin-mediated regioselective benzylation and allylation of polyols: Applicability of a catalytic approach under solvent-free conditions

The first catalytic version of the stannylene-mediated benzylation and allylation of polyols is reported. The methodology is based on a simple solvent-free protocol that significantly advances, in terms of both experimental ease and synthetic scope, the a

Modifying the regioselectivity of glycosynthase reactions through changes in the acceptor

Successful glycosynthase-mediated reactions have been performed on 6-O-benzyl-, 6-O-(4-nitrobenzyl)-, and 6-O-benzoyl-D-glucopyranose to give 1,2-β- and 1,3-β-D-glycosylated products; 4-O-benzyl-D-xylopyranose gave only a 1,2-β-glycosylated product. A rat

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