147687-33-0

Upstream product

• 40653-32-5 methyl 2,3,4-tri-O-benzyl-β-D-galactopyranoside 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 40653-30-3 methyl 2,3,4-tri-O-benzyl-6-O-triphenylmethyl-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 1824-94-8 methyl beta-D-galactopyranoside 
• 6988-40-5 methyl 2,3-di-O-benzyl-β-D-galactopyranoside 
• 18311-26-7 methyl 6-O-triphenylmethyl-β-D-galactopyranoside 
• 4356-80-3 methyl 2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 529493-92-3 2-(acetoxymethyl)-6-bromotetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 86520-63-0 2,3,4,6-tetra-O-acetyl-α-galactopyranosyl trichloroacetimidate 
• 67583-56-6 Methyl 2,3,4-O-tri-O-benzyl-6-O-triphenylmethyl-β-D-glucopyranoside 
• 67412-01-5 Methyl 6-O-triphenylmethyl-β-D-glucopyranoside 
• 709-50-2 methyl beta-D-glucopyranoside 

Downstream Products

• 108671-41-6 (2R,3R,4S,5R,6R)-2-Hydroxymethyl-6-((2R,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3,4,5-triol 
• 161518-48-5 Methyl 2,3,4-tri-O-benzyl-6-O-(β-D-galactopyranosyl)-β-D-glucopyranoside 

Relevant academic research and scientific papers

SYNTHESIS OF METHYL 2-O-, 3-O-, 4-O-, 6-O-, 2,3-DI-O- AND 4,6-DI-O-β-D-GALACTOPYRANOSYL-β-D-GLUCOPYRANOSIDE

Synthesis of methyl O-β-D-galactopyranosyl-(1->2)-β-D-glucopyranoside 1, methyl O-β-D-galactopyranosyl-(1->3)-β-D-glucopyranoside 2, methyl O-β-D-galactopyranosyl-(1->4)-β-D-glucopyranoside 3, methyl O-β-D-galactopyranosyl-(1->6)-β-D-glucopyranoside 4, me

The function of the 5-hydroxymethyl group of lactose in enzymatic hydrolysis with beta-galactosidase from E. coli.

A series of 6-substituted methyl lactoside derivatives together with methyl allolactoside and (6S)-methyl [6-2H]lactoside have been synthesized and characterized by NMR spectroscopy. All compounds were tested as substrates for the enzyme beta-galactosidas

PREPARATION OF α AND Β ANOMERS OF VARIOUS ISOMERIC METHYL O-D-GALACTOPYRANOSYL-D-GALACTOPYRANOSIDES. STANDARDS FOR INTERPRETATION OF 13C-N.M.R. SPECTRA OF D-GALACTOPYRANANS

The four isomer of methyl O-β-D-galactopyranosyl-β-D-galactopyranoside were prepared by condensation of 2,3,4,6-tetra-O-acetyl-α-galactopyranosyl bromide with appropriate, partially O-substitued derivatives of methyl β-D-galactopyranoside.Reaction of 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-α-D-galactopyranose with the same acceptors, in the presence of mercuric bromide, led to the formation of α and β linkages.Thus, it was possible to assign 13C-n.m.r. resonances of α and β anomers of methyl O-D-galactopyranosyl-β-D-galactopyranosides.In terms of application of these shift values and those of related D-galactobioses to the structual analysis of D-galactopyranans by shift comparisons, some generalizations can be made.For β-D-galactopyranans, the resonances glycosyloxylated carbon atoms of methyl O-β-D-galactopyranosyl-β-D-galactopyranosides are sensitive to structure and appear to have typical values, whereas limited variation was observed with shift of C-1' signals.On the other hand, for assigning structures to D-galactopyranans containing α linkages, the C-1' shifts (at higher field) of methyl O-α-D-galactopyranosyl-β-D-galactopyranosidesc are sensitive to linkage position, whereas those of glycosyloxylated carbon atoms vary only a little.