74517-40-1

Upstream product

• 4704-15-8 ((2S,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-carbamic acid benzyl ester 
• 93000-10-3 benzyl ((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-6-methoxy-2-phenyl hexahydropyrano[3,2-d][1,3]dioxin-7-yl)carbamate 
• 108-24-7 acetic anhydride 
• 106265-18-3 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone 
• 129095-43-8 methyl 4,6-O-benzylidene-3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonyl-amino)-2-deoxy-α-D-glucopyranoside 
• 102997-59-1 2-amino-N-benzyl-N-benzyloxycarbonyl-3,4-di-O-benzyl-2-deoxy-1-O-methyl-α-D-gluco-hex-5-enopyranoside 
• 129117-17-5 methyl 3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonylamino)-2,6-dideoxy-6-iodo-α-D-glucopyranoside 
• 129095-44-9 methyl 3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonylamino)-2-deoxy-α-D-glucopyranoside 
• 121843-64-9 1D-(1,2,4/3) 3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-methoxymethylene-1,3,4-cyclohexanetriol 
• 102562-01-6 (1R,4S,5S,6S,8R,9R)-4,5-epoxy-8,9-isopropylidenedioxy-7-oxabicyclo<4.3.0>nonan-3-one 
• 246034-43-5 carba-α-D-glucosamine 
• 106265-22-9 (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 

Downstream Products

• 125324-50-7 DL-(1,2,3,5/4)-2-acetamido-5-(hydroxymethyl)-1,3,4-cyclohexanetriol 
• 125324-50-7 DL-(1,4/2,3,5)-2-acetamido-5-(hydroxymethyl)-1,3,4-cyclohexanetriol 
• 125324-50-7 DL-(1,3,5/2,4)-2-acetamido-5-(hydroxymethyl)-1,3,4-cyclohexanetriol 
• 125324-50-7 DL-(1,2/3,4,5)-2-acetamido-5-(hydroxymethyl)-1,3,4-cyclohexanetriol 

Relevant academic research and scientific papers

SYNTHETIC METHODS FOR THE PREPARATION OF BASIC D- AND L-PSEUDO-SUGARS. SYNTHESIS OF CARBOCYCLIC ANALOGUES OF N-ACETYL-MURAMYL-L-ALANYL-D-ISOGLUTAMINE (MDP)

Two exocyclic olefins 10 and 22, readily elaborated from D-glucosamine, have been transformed by Ferrier rearrangement reaction into aminocyclohexanones 11, 12 and 23, 24.Reduction of ketone 11 with tri-t-butoxy-aluminium hydride followed by sequential ac

SYNTHESIS OF SEVEN PENTA-N,O-ACETYL-PSEUDO-2-AMINO-2-DEOXY-DL-HEXOPYRANOSES

The 1,5-dialdehyde generated through periodate oxidation of 4,7-O-isopropylidene-pseudo-α-DL-galactopyranose (3) undergoes base-catalysed cyclisation with nitromethane to give three crystalline pseudo-2-deoxy-2-nitro-DL-hexopyranose derivatives with the β

New Synthesis of Penta-N,O-acetyl-DL-validamine and Pseudo-2-amino-2-deoxy-α-DL-mannopyranose, and Their Uronate Analogs

Treatment of the hydroxy lactone derived from (+/-)-endo-7-oxabicyclohept-5-ene-2-carboxylic acid with hydrogen bromide-acetic acid, followed by esterification, gave 48 percent of ethyl DL-(1,3,5/2,4)-5-bromo-2,3,4-trihydroxy-1-cyclohexanecarboxyla

Construction of an Optically Active 7-Oxabicyclonon-4-en-3-one. Skeleton from D-Glucose, and Its Transformation to Some Pseudo-Hexopyranoses

A versatile chiral compound, (1R,6R,8R,9R)-8,9-isopropylidenedioxy-7-oxabicyclonon-4-en-3-one (6), was efficiently synthesized from D-glucose.The synthesis featured an intramolecular aldol cyclization of 3-C-acetylmethyl-3-deoxy-1,2-O-isopropyliden

Synthesis of Carbocyclic Analogues of D-Glucosamine and L-Idosamine from D-Glucosamine

Derivatives of pseudo-D-glucosamine and pseudo-L-idosamine have been prepared from the chiral cyclohexanone (1) by a short sequence, including methoxy-methylenation or methylenation, followed by stereoselective oxymercuration or hydroboration, respectivel