73683-78-0

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 38099-78-4 exo-Benzyl-3,4-O-benzylidene-β-L-arabinopyranoside 
• 100-39-0 benzyl bromide 
• 81692-00-4 benzyl 2-O-benzyl-endo-3,4-O-benzylidene-β-L-arabinopyranoside 
• 81691-99-8 benzyl 2-O-benzyl-exo-3,4-O-benzylidene-β-L-arabinopyranoside 
• 7473-38-3 benzyl β-L-arabinopyranoside 
• 79936-13-3 benzyl exo-3,4-O-benzylidene-β-L-arabinopyranoside 
• 79936-12-2 benzyl endo-3,4-O-benzylidene-β-L-arabinopyranoside 
• 100-44-7 benzyl chloride 
• 74660-31-4 benzyl 2,3-di-O-benzoyl-4-O-methylthiomethyl-β-L-arabinopyranoside 
• 73683-75-7 benzyl 3-O-(methylthio)methyl-β-L-arabinopyranoside 
• 18403-13-9 Benzyl 2,3-di-O-benzoyl-β-L-arabinopyranoside 
• 73683-76-8 benzyl 2,3-di-O-benzyl-4-O-methylthiomethyl-β-L-arabinopyranoside 

Downstream Products

• 73683-99-5 benzyl 2,3-di-O-benzyl-β-L-threo-pentopyranosid-4-ulose 
• 79936-21-3 benzyl 2,3-di-O-benzyl-4-O-methyl-β-L-arabinopyranoside 

Relevant academic research and scientific papers

Regioselective ring opening of exo- and endo-3,4-benzylidene acetals of arabinopyranoside derivatives with Lewis acids and reducing agents

Dioxolane type 3,4-benzylidene acetals of benzyl β-l-arabinose either as a mixture or pure exo- and endo-isomers cleavaged with BF3· OEt2/Et3SiH in dichloromethane or acetonitrile regioselectively, provided the 4-O-benzyl-

STEREOSELECTIVE HYDROGENOLYSIS OF DIOXOLANE-TYPE BENZYLIDENE ACETALS; PREPARATION OF MONO- AND DI-O-BENZYL ETHERS OF BENZYL β-L-ARABINOPYRANOSIDE

Both isomers (2 and 3) of benzyl 3,4-O-benzylidene-β-L-arabinopyranoside, their 2-O-benzyl- (4 and 5), 2-O-allyl (6 and 7) and 2-O-p-toluenesulfonyl (8 and 9) derivatives were prepared and hydrogenolyzed with LiAlH4-AlCl3 reagent.The exo-isomers (2, 4, 6)

Branched-chain Sugars. XXII. Synthesis of Benzyl 2,3-Di-O-benzyl- and 2,3-O-Methylene-β-L-threo-pentopyranosid-4-uloses, and the Corresponding 6-Deoxy-α-D-xylo-hexopyranosid-4-uloses

The title compounds were synthesized from L-arabinose and D-glucose as intermediates to a few naturally occurring branched-chain sugars.Oxidation conditions of precursors to the corresponding 4-uloses were examined.