85248-08-4

Upstream product

• 121687-43-2 C₃₆H₃₇⁽²⁾HO₆ 
• 121687-41-0 4,5,6,8-tetra-O-benzyl-3,7-anhydro-1-deoxy-D-glycero-D-gulo-2-octulose 2,2-dimethyl acetal 
• 121687-36-3 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-D-glycero-D-gulo-2-octulose 
• 121687-40-9 4,5,6,8-tetra-O-acetyl-3,7-anhydro-1-deoxy-D-glycero-D-gulo-2-octulose 2,2-dimethyl acetal 
• 100-39-0 benzyl bromide 
• 98-59-9 p-toluenesulfonyl chloride 
• 85230-74-6 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-2-deuterio-D-erythro-L-talo-octilol 
• 85230-74-6 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-2-deuterio-D-erythro-L-galacto-octilol 
• 85230-74-6 C₃₆H₃₉⁽²⁾HO₆ 
• 71420-08-1 1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)imidazolidine 
• 85230-62-2 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-D-threo-L-galacto-octitol 
• 85280-49-5 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-D-threo-L-talo-octitol 
• 85230-61-1 1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)-1,3-diphenylimidazolidine 
• 85230-73-5 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1-deoxy-D-glycero-L-manno-octulose 

Downstream Products

• 121687-43-2 ethylene oxide 1,2:3,7-dianhydro-4,5,6,8-tetra-O-benzyl-2-deuterio-D-erythro-L-galacto-octitol 
• 121687-43-2 ethylene oxide 1,2;3,7-dianhydro-4,5,6,8-tetra-O-benzyl-2-deuterio-D-erythro-L-talo-octitol 
• 121687-42-1 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1,2-dideoxy-2-deuterio-D-glycero-D-gulo-oct-1-enitol 
• 121687-38-5 (Z)-4,5,6,8-tetra-O-benzyl-3,7-anhydro-1,2-dideoxy-2-deuterio-D-gluco-oct-2-enitol 
• 85230-75-7 4,5,6,8-tetra-O-acetyl-3,7-anhydro-1-deoxy-2-deuterio-2-O-p-tolylsulfonyl-D-threo-L-galacto-octitol 

Relevant academic research and scientific papers

SYNTHESIS OF (Z)-3,7-ANHYDRO-1,2-DIDEOXY-2-DEUTERIO-D-gluco-OCT-2-ENITOL, A PROCHIRAL SUBSTRATE FOR PROBING THE CATALYTIC FUNCTIONING OF GLUCOSYLASES

Synthesis of the title compound provides a prochiral, glycosyl-donor substrate well suited for use as a probe of the catalytic functioning of D-glucosyl-mobilizing enzymes, because the full stereochemistry of enzymic reactions at its double bond may be un

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-