123044-80-4

Upstream product

• 123044-78-0 (S)-2-Benzyloxy-2-((4R,5R)-5-hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol 
• 40031-40-1 3,4-O-isopropylidene-L-arabinono-1,5-lactone 
• 100-39-0 benzyl bromide 
• 58645-35-5 3,4-O-isopropylidine L-arabinopyranose 
• 886025-69-0 2-O-benzyl-L-arabinose 

Downstream Products

• 541548-46-3 3-O-benzyl-1,2:4,5-di-O-isopropylidene-β-L-fructopyranose 

Relevant academic research and scientific papers

Iodomethyl group as a hydroxymethyl synthetic equivalent: Application to the syntheses of D-manno-hept-2-ulose and L-fructose derivatives

The one-carbon elongation of aldoses to ketoses using iodomethyllithium as the key reagent in the homologation step is exemplified by the preparation of two carbohydrates of chemical and biological interests: D-manno-hept-2-ulose from D-mannose and L-fructose from L-arabinose.

Highly Selective Synthesis of Aldonolactones from Protected Alditols by Ruthenium Complex-Catalyzed Dehydrogenation. A Method of Converting Aldopentoses to Their Strereoisomers

Highly selective hydrogen transfer reaction of substituted diols catalyzed by RuH2(PPh3)4 was applied to the conversion of aldopentoses into their stereoisomers via protected pentitols.Thus, the selective transformations of L-arabinose and L-ribose into p