118014-53-2

Upstream product

• 117918-35-1 2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethylene)-malonic acid dimethyl ester 
• 117918-36-2 methyl 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-6-C-(methoxycarbonyl)-α-D-xylo-hepto-1,4-furanuronate 
• 117918-37-3 2-((2R,3R,4R)-3-Benzyloxy-4,5-dihydroxy-tetrahydro-furan-2-ylmethyl)-malonic acid dimethyl ester 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 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 

Downstream Products

• 117918-40-8 (1S,2S,3S,4R)-3-(benzyloxy)-2,4-dihydroxycyclopentane-1-methanol 
• 118013-60-8 (1R,2R,3S,4R)-3-(benzyloxy)-2,4-dihydroxycyclopentane-1-methanol 
• 117918-40-8 (1R,2S)-2-Benzyloxy-4-hydroxymethyl-cyclopentane-1,3-diol 
• 118013-55-1 (1S,2S,3S,4R)-2,3,4-trihydroxycyclopentane-1-methanol 
• 118013-58-4 Acetic acid (2S,3R)-3-acetoxy-5-acetoxymethyl-2-benzyloxy-cyclopentyl ester 
• 117918-39-5 methyl (3R,4R)-3-(benzyloxy)-4-hydroxy-1-cyclopentene-1-carboxylate 
• 118013-57-3 (3R,4R)-3-(benzyloxy)-4-hydroxy-1-cyclopentene-1-methanol 
• 118013-56-2 (1R,2S,3R,4R)-4-(hydroxymethyl)cyclopentae-1,2,3-triol 

Relevant academic research and scientific papers

Syntheses of (1S,2S,3S,4R)- and (1R,2R,3S,4R)-2,3,4-Trihydroxycyclopentane-1-methanol, Carbocyclic Analogues of α-L-Arabinofuranose and β-D-Ribofuranose

The title compounds, two carbocyclic analogues of aldopentofuranoses, were synthesized from D-glucose.The key cyclopentane ring formation was achieved under the glycol cleavage reaction of methyl 3-O-benzyl-5,6-dideoxy-6-C-(methoxycarbonyl)-D-xylo-hepto-1