85230-63-3

Upstream product

• 85230-62-2 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-D-threo-L-galacto-octitol 
• 98-59-9 p-toluenesulfonyl chloride 
• 85280-49-5 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-D-threo-L-talo-octitol 
• 71420-08-1 1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)imidazolidine 
• 85230-61-1 1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)-1,3-diphenylimidazolidine 
• 100-39-0 benzyl bromide 
• 91738-16-8 1,3-Diphenyl-2-((2S,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-imidazolidine 
• 74281-68-8 3,4,5,7-Tetra-O-acetyl-2,6-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-D-glycero-D-gulo-heptose 
• 113019-43-5 2,3,4,6-tetra-O-benzyl-1-formyl-D-glucopyranose 
• 91797-40-9 3,7-Anhydro-4,5,6,8-tetra-O-benzyl-1-desoxy-D-erythro-L-talo-octitol 
• 91797-39-6 3,7-Anhydro-4,5,6,8-tetra-O-benzyl-1-desoxy-D-erythro-L-galacto-octitol 

Downstream Products

• 85230-64-4 4,5,6,8-Tetra-O-acetyl-3,7-anhydro-1-desoxy-2-O-(p-tolylsulfonyl)-D-erythro-L-galacto-octitol 
• 85230-64-4 4,5,6,8-Tetra-O-acetyl-3,7-anhydro-1-desoxy-2-O-(p-tolylsulfonyl)-D-erythro-L-talo-octitol 
• 85230-64-4 4,5,6,8-tetra-O-acetyl-3,7-anhydro-1-deoxy-2-O-p-tolylsulfonyl-D-threo-L-talo-octitol 
• 91738-18-0 Toluene-4-sulfonic acid (S)-1-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-ethyl ester 
• 91738-18-0 Toluene-4-sulfonic acid (R)-1-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-ethyl ester 
• 91738-18-0 3,7-anhydro-1-deoxy-2-O-p-tolylsulfonyl-D-threo-L-talo-octitol 

Relevant academic research and scientific papers

Reactions of Enolic Sugar Derivatives, XVI. - Synthesis of a Diastereotopic Proton Probe for α- and β-D-Glucosylases

For the elucidation of the stereochemistry in glucosylase-catalyzed proton addition reactions (Z)-3,7-anhydro-1,2-dideoxy-D-gluco-oct-2-enitol (1) was synthesized.Starting material for the multistep synthesis is 3,4,5,7-tetra-O-acetyl-2,6-anhydro-1-C-(1,3

DIASTEREOTOPIC SUBSTRATES OF β-D-GALACTOSIDASE FROM Escherichia coli AS PROBES FOR A CATALYTICALLY ACTIVE, PROTONATING GROUP

With 3,4,5,7-tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptonitrile as the starting material, the diastereotopic, enolic sugar derivatives (Z)-3,7-anhydro-2-deoxy-D-galacto-oct -2-enononitrile (2) and (Z)- (5) and (E)-3,7-anhydro-1,2-dideoxy-D-galacto-