149557-49-3

Upstream product

• 4258-02-0 2,3:5,6-di-O-isopropylidene-D-glucose diethyl dithioacetal 
• 100-39-0 benzyl bromide 

Downstream Products

• 163456-89-1 N-benzyl-(6R,1'S,2'R,3'R,4'R)-6-(3'-O-benzyl-1',2':5',6'-di-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one 
• 163456-90-4 N-benzyl-(2R,4S,1'S,2'R,3'R,4'R)-4-hydroxy-2-(3'-O-benzyl-1',2':5',6'-di-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)piperidine 
• 163456-91-5 N-benzyl-(2R,4S,1'S,2'R,3'R,4'R)-4-hydroxy-2-(3'-O-benzyl-1',2'-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)piperidine 
• 163456-92-6 (S)-[(4R,5S)-5-((2R,4S)-1-Benzyl-4-hydroxy-piperidin-2-yl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-benzyloxy-acetaldehyde 
• 163456-93-7 (2S,3R,4S)-4-((2R,4S)-1-Benzyl-4-hydroxy-piperidin-2-yl)-2-benzyloxy-3,4-dihydroxy-butyraldehyde 
• 359642-20-9 1L(1,2,4/3,5)-1-O-acetyl-2-O-benzyl-5-benzyloxyamino-3,4-O-isopropylidenecyclohexan-1,2,3,4-tetrol 
• 359642-18-5 5-O-acetyl-4-O-benzyl-6-bromo-6-deoxy-2,3-O-isopropylidene-D-glucose O-benzyloxime 
• 359642-16-3 5-O-acetyl-4-O-benzyl-6-bromo-6-deoxy-2,3-O-isopropylidene-D-glucose diethyl dithioacetal 
• 359642-19-6 1L(1,2,4/3,5)-1-O-acetyl-2-O-benzyl-3,4-O-isopropylidene-5-C-methoxycarbonylmethylcyclohexan-1,2,3,4-tetrol 
• 359642-17-4 methyl 7-O-acetyl-4-O-benzyl-8-bromo-2,3,8-trideoxy-4,5-O-isopropylidene-D-gluco-oct-2-enonate 
• 359642-15-2 4-O-benzyl-6-bromo-6-deoxy-2,3-O-isopropylidene-D-glucose diethyl dithioacetal 
• 359642-13-0 Acetic acid (1S,2S)-2-benzyloxy-1-bromomethyl-2-((4S,5R)-5-formyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethyl ester 
• 359642-14-1 4-O-benzyl-2,3-O-isopropylidene-D-glucose diethyl dithioacetal 
• 163456-88-0 4-O-benzyl-2,3:5,6-di-O-isopropylidene-aldehydo-D-glucose 

Relevant academic research and scientific papers

Cycloaddition Reactions of Carbohydrate Derivatives. Part VI. Quinolizidine Analogs of Castanospermine

Octahydroquinolizine-1,2,3,8-tetraols 12, 16 and 23, analogs of castanospermine, were synthesized from D-glucose, L-arabinose and D-mannose, respectively, using hetero-Diels-Alder reactions of sugar-derived azomethines as the key step.

Stereoelectronic Effects in the 6-Exo Free Radical Cyclization of Acyclic Sugar Derivatives: Synthesis of Branched Chain Cyclitols

The synthesis and free radical carbocyclization (Bu3SnH + AIBN) of acyclic sugar derivatives 1 - 12 is reported.The yields of these 6-exo cyclization processes are good and the diastereomeric excesses are from moderate to excellent.The resulting cyclohexanes are polyoxygenated, enantiomerically pure building blocks for the synthesis of complex branched chain cyclitols.The results obtained in the cyclization of radical precursors 1, 4, 6, and 8 are in sharp contrast with the results observed in the ring closure of compounds 2, 3, 5, and 7.An electron-attracting group (acetate or mesylate), located in a vicinal position to the carbon-centered radical, modifies the conformation of the reacting species in the transition state and thus changes the stereochemical outcome of the cyclization.This allowed us to select the nature of the absolute configuration at the newly formed stereocenter by simply changing the type of the substituents at the vicinal carbon where the radical is generated.