98098-96-5

Upstream product

• 58527-89-2 benzyl 1,2,3,6-tetra-O-benzyl-α-D-glucopyranoside 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 57783-81-0 Benzyl 2,3,6-tri-O-benzyl-β-D-galactopyranoside 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 74801-06-2 benzyl 2,3-di-O-benzyl-4,6-ol-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 88559-77-7 (2R,3R,4S,5R,6S)-2-Hydroxymethyl-6-((2R,3S,4S,5R,6R)-4,5,6-tris-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3,4,5-triol 

Relevant academic research and scientific papers

STANNOUS TRIFLATE MEDIATED GLYCOSIDATIONS. A STEREOSELECTIVE SYNTHESIS OF β-D-GLUCOSIDES.

Various 1,2 trans, β-D-linked disaccharides with glucose as non-reducing unit have been prepared with complete stereoselectivity from acetobromoglucose and suitably protected sugar derivatives using stannous triflate as promoter.

SYNTHESIS AND CHROMATOGRAPHIC PROPERTIES OF ISOMERIC O-β-D-GALACTOPYRANOSYL-D-GALACTOSES, AND OF DIASTEREOISOMERS OF 3,4-O- AND 4,6-O-(1-CARBOXYETHYLIDENE)-D-GALACTOSE

Partial hydrolysis of β-D-galactopyranans and D-galactose-containing polysaccharides having pyruvic acetal groups gives isomeric O-β-D-galactopyranosyl-D-galactoses and O-(1-carboxyethylidene)-D-galactoses, respectively.Their chromatographic properties in