478487-92-2

Upstream product

• 874-60-2 4-methyl-benzoyl chloride 
• 344905-99-3 6-O-(4-toluoyl)-1,2:3,4-di-O-isopropylidene-β-D-psicofuranose 
• 34626-95-4 1,2:3,4-di-O-isopropylidene-β-D-psicofuranose 
• 124-63-0 methanesulfonyl chloride 
• 478487-91-1 4-Methyl-benzoic acid (3aR,4R,6R,6aR)-6-hydroxymethyl-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 

Downstream Products

• 478487-95-5 4-Methyl-benzoic acid (2R,3R,4R)-3,4,5-triacetoxy-5-methanesulfonyloxymethyl-tetrahydro-furan-2-ylmethyl ester 
• 478487-94-4 4-Methyl-benzoic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-methanesulfonyloxymethyl-5-methoxy-tetrahydro-furan-2-ylmethyl ester 
• 478487-98-8 4-Methyl-benzoic acid (2R,3R,4R)-3,4-diacetoxy-5-bromo-5-methanesulfonyloxymethyl-tetrahydro-furan-2-ylmethyl ester 
• 478488-01-6 C₂₃H₂₄O₇ 
• 478487-93-3 methyl 1-O-mesyl-5-O-toluoyl-β-D-psicofuranoside 

Relevant academic research and scientific papers

Synthesis and anti-HCV activity of 1-(1′,3′-O-anhydro-3′-C-methyl-β-d-psicofuranosyl)uracil

Synthesis of a novel 1′,2′-oxetane-uridine bearing a 2′-C-methyl substituent, [1-(1′,3′-O-anhydro-3′-C-methyl-β-d-psicofuranosyl)uracil], is described. Key to its construction was the use of 6-O-(p-toluoyl)-1,2:3,4-di-O-isopropylidene-3-C-methyl-d-psicofu

Synthesis of anhydro psicofuranosyl nucleosides

Methyl 1-O-mesyl-5-O-toluoyl-β-D-psicofuranoside (5) was synthesised from the known 1,3;4,5-di-O-isopropylidene-β-D-psicofuranose (1) as a key carbohydrate precursor for the preparation of anhydro psicofuranosyl nucleosides. Transformation of 5 into aceta