360562-22-7

Upstream product

• 57575-19-6 2-[(3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 19877-13-5 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-enofuranose 
• 360562-21-6 6-O-Benzoyl-3-O-benzyl-1,2-O-isopropylidene-5-O-[(methylsulfanyl)thiocarbonyl]-α-D-glucofuranose 
• 37776-15-1 6-O-Benzoyl-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 360562-24-9 Diethyl (3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hexofuranos-6-yl)malonate 
• 360562-23-8 3-O-Benzyl-5-deoxy-1,2-O-isopropylidene-6-iodo-α-D-xylo-hexofuranose 

Relevant academic research and scientific papers

A stereoselective approach for the total synthesis of (-)-tadanalactam from acetonide-d-glucose

A stereoselective and realistic approach for the total synthesis of naturally occurring δ-lactam (-)-tadanalactam, has been accomplished from the commercially existing acetonide-d-glucose involving Birch reduction, Pinnick oxidation, Staudinger reaction,

Synthesis of carba analogues of deoxy-4-C-(hydroxymethyl)-hexopyranoses, intermediates in the synthesis of carbocyclic nucleosides

3-O-Benzyl-1,2-O-isopropylidene-α-D-glucofuranose-5,6-O-sulfate (1) was treated with sodium salt of dimethyl malonate to obtain, after hydrolysis, methyl 5-(3-O-benzyl-1,2-O-isopropylidene-α-D-erythrofuranos-4-yl)-2- oxotetrahydrofuran-3-carboxylate (3) w