341553-93-3

Upstream product

• 100-39-0 benzyl bromide 
• 192118-38-0 (1R,2R,3S,4S)-4-(tert-butoxymethyl)-2,3-(isopropylidenedioxy)cyclopentan-1-ol 

Downstream Products

• 341553-95-5 (2R,3R,3aS,9aS)-2-Benzyloxy-5,5,7,7-tetraisopropyl-hexahydro-4,6,8-trioxa-5,7-disila-cyclopentacycloocten-3-ol 
• 341554-01-6 Benzoic acid (1R,2S,4R)-2-(tert-butyl-dimethyl-silanyloxymethyl)-4-(tetrahydro-pyran-2-yloxy)-cyclopentyl ester 
• 341553-96-6 (2R,3aR,9aS)-2-Benzyloxy-5,5,7,7-tetraisopropyl-hexahydro-4,6,8-trioxa-5,7-disila-cyclopentacyclooctene 
• 341554-02-7 Benzoic acid (1R,2S,4R)-2-hydroxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclopentyl ester 
• 855662-72-5 (+)-(2R,4R)-1-difluoro-2-O-benzyloxy-4-(O-trityloxymethyl)cyclopentane 
• 855662-70-3 (+)-(1R,2S,4R)-1-O-benzyloxy-2-hydroxyl-4-(O-trityloxymethyl)cyclopentane 
• 855662-71-4 (+)-(2R,4R)-2-O-benzyloxy-4-(O-trityloxymethyl)cyclopentan-1-one 
• 855662-73-6 (+)-(3R,5R)-1-fluoro-5-O-benzyloxy-3-(O-trityloxymethyl)cyclopent-1-ene 
• 855662-78-1 (+)-(3R,5R)-1-fluoro-3-(O-tert-butyldimethylsilyloxymethyl)-5-O-benzyloxycyclopent-1-ene 
• 855662-68-9 (+)-(1R,2S,4R)-1-O-benzyloxy-2-hydroxyl-4-hydroxymethylcyclopentane 
• 855662-75-8 (+)-(3R,5R)-1-fluoro-3-hydroxymethyl-5-O-benzyloxycyclopent-1-ene 
• 341553-94-4 (-)-(1R,2S,3S,4R)-1-O-benzyloxy-2,3-dihydroxyl-4-hydroxymethylcyclopentane 

Relevant academic research and scientific papers

Solid Phase Synthesis of Carbocyclic L-2′-Deoxynucleosides

matrix presented Carbocyclic L-2'deoxynucleosides 17 were synthesized on solid phase in four steps from the appropriately protected intermedate 11. The Mitsunobu reaction was used as a condensation method between the carbocyclic moiety and heterocyclic ba