91852-34-5

Upstream product

• 20764-63-0 β-cellobioseoctaacetate 
• 1252764-09-2 2-deoxy-2-azido-1α-trichloroacetamido-hexa-O-acetyl cellobioside 
• 100-51-6 benzyl alcohol 
• 225242-63-7 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(tetra-O-acetyl-β-D-glucopyranosyl)-α-β-D-glucopyranosyl nitrate 
• 91878-42-1 2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl-(1→4)-3,6-di-O-acetyl-2-azido-2-deoxy-1-O-nitro-β-D-glucopyranose 
• 67314-36-7 3,6-di-O-acetyl-4-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl]-2-deoxy-D-arabino-hex-1-enopyranose 
• 91852-33-4 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(tetra-O-acetyl-β-D-glucopyranosyl)-α-D-glucopyranosyl bromide 
• 92840-69-2 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-α-D-glucopyranosyl chloride 

Downstream Products

• 91852-36-7 benzyl 2-amino-2-deoxy-4-O-(β-D-glucopyranosyl)-β-D-glucopyranoside 
• 91852-23-2 2-[(2R,3R,4R,5S,6R)-2-Benzyloxy-4-hydroxy-6-hydroxymethyl-5-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 91852-35-6 benzyl 2-azido-2-deoxy-4-O-(β-D-glucopyranosyl)-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis and evaluation of 2-deoxy-2-amino-β-cellobiosides as cellulase inhibitors

The cellulase mixture of Hypocrea jecorina (formerly Trichoderma reesei) contains a variety of exo- and endoglucanases that belong to different structural families. As such, these enzymes form an interesting model system to study the enzyme-ligand interac

SYNTHESIS OF BENZYL 2-AZIDO-2-DEOXY-4-O-β-D-GLUCOPYRANOSYL-α-D-GLUCOPYRANOSIDE AND 1,6-ANHYDRO-2-AZIDO-2-DEOXY-4-O-β-D-GLUCOPYRANOSYL-β-D-GLUCOPYRANOSE

The title compounds were prepared from cellobiose by means of two series of transformations.One series entailed the azidonitration of 3,6-di-O-acetyl-1,5-anhydro-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-arabino-hex-1-enitol to give 3,6-di

The synthesis of derivatives of lactosamine and cellobiosamine to serve as probes in studies of the combining site of the monoclonal anti-I Ma antibody

Syntheses are reported for a variety of structures used in a continuation of our studies of the combinig site of the monoclonal anti-I Ma antibody.These structures include that N-acetyl, N-formyl, and N-pivalyl derivatives of methyl-β-D-lactosaminide, the ethyl, propyl, isopropyl, and isobutyl β-glycosides of N-acetyllactosamine and the βDGal(1->4)βDGlcNAc(1->6)-, βDGal(1->4)βDGlcNH2(1->6)-, βDGal(1->4)βDGlcNCOCF3(1->6)-, and βDGlc(1->4)βDGlcNAc(1->6)-derivatives of 1,2;3,4-di-O-isopropylidene-α-D-galactopyranose.Also, preparations of 6-deoxy-βDGal(1->4)βDGlcNAc(1->6)α,βDGal and βDGlcNAc(1->6)βDGal(1->4)βDGlcNAcOCH3 are described.