50615-76-4

Upstream product

• 61-58-5 2-deoxy-D-arabino-hexopyranose 
• 100-51-6 benzyl alcohol 
• 13265-84-4 D-glucal 
• 79698-04-7 benzyl 3,4,6-tri-O-acetyl-2-bromo-2-deoxy-α-D-mannopyranoside 
• 2873-29-2 D-glucal triacetate 
• 79698-05-8 phenylmethyl 3,4,6-tri-O-acetyl-2-deoxy-α-D-arabinohexopyranose 

Downstream Products

• 79774-61-1 benzyl 3,4-di-O-benzyl-2,6,7-trideoxy-7-diethoxyphosphinoyl-α-D-arabino-hept-6-trans-enopyranoside 
• 79774-69-9 benzyl 3,4-di-O-benzyl-2,6-dideoxy-6-diethoxyphosphinoyl-α-D-arabino-hexopyranoside 
• 79774-57-5 benzyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-arabino-hexopyranoside 
• 79774-60-0 benzyl 3,4-di-O-benzyl-2-deoxy-α-D-arabino-hexodialdo-1,5-pyranoside 
• 79774-68-8 benzyl 3,4-di-O-benzyl-6-bromo-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 79774-58-6 benzyl 3,4-di-O-benzyl-2-deoxy-α-D-arabini-hexopyranoside 
• 79774-59-7 benzyl 3,6-di-O-benzyl-2-deoxy-α-D-arabino-hexopyranoside 
• 83021-80-1 benzyl 4,6-O-benzylidene-2-deoxy-3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-α-D-arabino-hexapyranoside 
• 83021-81-2 benzyl 4,6-O-benzylidene-2-deoxy-3-O-(β-D-glucopyranosyl)-α-D-arabino-hexopyranoside 
• 83021-82-3 benzyl 2-deoxy-3-O-(β-D-glucopyranosyl)-α-D-arabino-hexopyranoside 
• 75810-07-0 Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside 
• 79813-89-1 benzyl 4,6-O-benzylidene-2-deoxy-α-D-arabino-hexopyranoside 
• 145295-38-1 benzyl 6-bromo-2,6-dideoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Allylic strain as a stereocontrol element in the hydrogenation of 3-hydroxymethyl-cyclohex-3-en-1,2,5-triol derivatives. Synthesis of the carbasugar pseudo-2-deoxy-α-D-glucopyranose

By adaptation of a literature method developed in the glucose series and standard protecting group manipulations a 2-deoxy-D-glucose derivative is converted to a series of 1R,2R,5R-3-hydroxymethyl-cyclohexen-1,2,5-triol derivatives whose reduction to the

Enzymatic synthesis of alkyl α-2-deoxyglucosides by alkyl alcohol resistant α-glucosidase from Aspergillus niger

Aspergillus niger α-glucosidase (ANGase) was used for an efficient syntheses of alkyl α-d-2-deoxyglucosides (A2DGs) and for regioselectivity studies of alkoxy-hydro additions of d-glucal in the presence of alkyl alcohols. ANGase showed a high stability wi

Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: Synthesis of both enantiomers of high-carbon monosaccharides

An inversion of stereoselectivity in aldol condensations catalyzed by sialic acid aldolase (from Escherichia coli, Shinko American Inc.) was observed when L-mannose, 6-deoxy-L-mannose, L-talose, 2-deoxy-L-glucose, 2-deoxy-L-rhamnose, N-acetyl-L-mannosamin