158250-56-7

Upstream product

• 151693-58-2 (1R,2R,3S,4R,5R)-3,4-di-O-benzyl-5-benzyloxymethylcyclohexane-1,2,3,4-tetraol 
• 207564-34-9 (1S,5R,6R)-5,6-Bis-benzyloxy-cyclohex-3-enecarbaldehyde 
• 207564-33-8 (2S,3S,4R)-3,4-Bis-benzyloxy-3,4-dihydro-2H-pyran-2-carbaldehyde 
• 58871-10-6 3,4-di-O-benzyl-D-glucal 
• 207564-32-7 1,5-anhydro-di-O-benzyl-2,6,7-trideoxy-D-arabino-hept-1,6-dienitol 
• 100-39-0 benzyl bromide 
• 866916-65-6 tetra-O-acetyl-6,7-dideoxy-α-D-gluco-hept-6-enopyranose 
• 866916-82-7 tri-O-acetyl-6,7-dideoxy-α-D-gluco-hept-6-enopyranosyl bromide 
• 207564-31-6 1,5-anhydro-3,4-di-O-benzyl-2-deoxy-5a-carba-D-arabino-hex-1-enitol 

Downstream Products

• 207564-36-1 (1S,2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-cyclohexane-1,2-diol 
• 162119-26-8 2,3,4,6-tetra-O-benzyl-5a-carba-β-D-glucopyranose 
• 162019-95-6 (2S,3R,4E)-3-benzyloxy-1-(2,3,4,6-tetra-O-benzyl-5a-carba-β-D-glucopyranosyloxy)-2-(p-tolylsulfonylamino)-4-octadecene 
• 124330-57-0 (2R,3S,4R,5R)-2,3,4-tris(benzyloxy)-5-[(benzyloxy)methyl]cyclohexanone 
• 135820-00-7 5a-carba-α-D-mannopyranose 
• 152203-03-7 (1R,2R,3S,4R,5R)-1,2-anhydro-3,4-di-O-benzyl-5-benzyloxymethylcyclohexan-1,2,3,4-tetraol 

Relevant academic research and scientific papers

Chemoenzymatic syntheses of carbasugar analogues of nucleoside diphosphate sugars: UDP-carba-Gal, UDP-carba-GlcNAc, UDP-carba-Glc, and GDP-carba-Man

Chemoenzymatic syntheses of several NDP-carba-sugars have been successfully carried out, and these essential cofactor analogues are expected to be selective inhibitors of glycosyltransferase enzymes. The Royal Society of Chemistry.

The synthesis of a new class of potential inhibitors for glycoside hydrolases

Some attempts toward the synthesis of novel inhibitors of glycosyl transferases are described. More successfully, the synthesis of an activated cyclopropacyclohexene and an amide and an amine of a cyclopropa-fused pyranose are described. None of these three novel compounds proved to be a significant inhibitor of a retaining α-glucosidase from barley. Copyright Taylor & Francis, Inc.

Carbohydrates to carbocycles: An expedient synthesis of pseudo-sugars

A short and versatile synthesis of pseudo-sugars from sugars utilizing the Claisen rearrangement as the key step is described.

Synthesis and Glycosidase-inhibitory Activity of Cyclophellitol Analogues

The 6-deoxy-1,2-anhydro-analogues of cyclophellitol, 5 and 6, have been synthesised from diol 11 via regioselective ring opening of the cyclic sulfate 15, an internal SN2 reaction and hydrogenolysis.Compounds 5,6, cyclophellitol 1 and its diast