85735-13-3

Upstream product

• 39037-12-2 2-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1,3-diphenylimidazolidine 

Downstream Products

• 906102-84-9 C₃₀H₃₄N₂O₆S 
• 1352945-44-8 C₂₃H₂₈O₇S 
• 1352945-23-3 C₁₆H₂₂O₅ 
• 1352945-24-4 (3aR,4R,6S,6aS)-4-(benzyloxymethyl)-2,2,6-trimethyltetrahydrofuro-[3,4-d][1,3]dioxole 
• 86040-32-6 2-(5-O-benzyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1,3-diphenylimidazolidine 
• 86040-35-9 2-O-acetyl-3,6-anhydro-7-O-benzyl-4,5-O-isopropylidene-D-glycero-D-allo-heptonamide 
• 86040-36-0 2-O-acetyl-3,6-anhydro-7-O-benzyl-4,5-O-isopropylidene-D-glycero-D-altro-heptonamide 
• 86040-33-7 3,6-anhydro-7-O-benzyl-4,5-O-isopropylidene-D-glycero-D-allo-heptonamide 
• 86040-34-8 3,6-anhydro-7-O-benzyl-4,5-O-isopropylidene-D-glycero-D-altro-heptonamide 

Relevant academic research and scientific papers

An efficient total synthesis and absolute configuration determination of varitriol

The first total synthesis and the absolute configuration determination of varitriol are described. The Royal Society of Chemistry 2006.

Chiral transformations of D-ribose to 2-(β-D-ribofuranosyl)-L and D-glycine and an anhydroallose hemiacetal used in C-nucleoside synthesis

Conversion of D-ribose to the epimeric 3,6-anhydro-4,5,7-tri-O-benzyl-D-glycero-D-(allo and altro)-heptonamides (5) followed published methods.Mesylation of 5 allowed convenient separation of the 2-O-methanesulfonyl D-allo (6a) and D-altro (6b) diasterome