140397-44-0

Upstream product

• 1152661-05-6 2,6-anhydro-7,8,9-trideoxy-D-glycero-L-galacto-non-7,8-dienitol 
• 100-39-0 benzyl bromide 
• 3866-62-4 2,3,4,6-tetrakis-O-(phenylmethyl)-1-O-acetyl-α-D-galactopyranose 
• 13361-64-3 trimethyl(propargyl)silane 
• 53008-63-2 methyl 2,3,4,6-tetra-O-benzyl-α-D-galactopyranoside 

Downstream Products

• 140397-45-1 2,6-anhydro-3,4,5,7-tetra-O-benzyl-7,8,9-trideoxy-D-glycero-L-gluco-heptose 
• 140397-46-2 (2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)methanal 
• 140397-48-4 (2R,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-(diphenyl-phosphinoylmethyl)-tetrahydro-pyran 
• 140461-65-0 (2',3',4',6'-tetra-O-benzyl-β-D-galactopyranosyl)methyl alcohol 
• 260551-06-2 (2,6-anhydro-3,4,5,7-tetra-O-benzyl-D-glycero-L-gluco-heptit-1-yl) di-O-phenyl phosphate 
• 260551-05-1 2,6-anhydro-3,4,5,7-tetra-O-benzyl-D-glycero-L-gluco-heptitol 

Relevant academic research and scientific papers

Ultrasound-assisted synthesis of C-glycosides

A significant rate enhancement was observed in the preparation of allyl and allenyl-C-glycosides from glycosyl acetate or methyl O-glycoside precursors when ultrasound irradiation was employed as an energy source. The C-glycosides were obtained in 77-96%

Synthesis and conformational analysis of (α-D-Galactosyl) phenylmethane and α-,β-difluoromethane analogues: interactions with the plant lectin viscumin

(aα-D-Galactosyl)phenylmethane (1), (α- and β-D-galactosyl)-(difluoro)phenylmethane (2 and 3) have been prepared and their conformations in solution were described by using a combination of force-field calculations and NMR spectroscopic studies. Galactosi