120905-29-5

Upstream product

• 120905-28-4 (-)-(1R,6R,8R)-8-<(benzyloxy)methyl>-3-phenyl-2,4-dioxabicyclo<4.3.0>nonane 
• 108275-94-1 (-)-(1R,6R,8R)-3-phenyl-2,4-dioxabicyclo<4.3.0>nonane-8-methanol 
• 3396-11-0 cesium acetate 
• 116142-70-2 (-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate 
• 120236-98-8 (-)-(1R,2R,4R)-4-<(benzyloxy)methyl>-2-hydroxycyclopentanemethanol 

Downstream Products

• 120905-32-0 (+)-(1R,3S,4R)-3-acetoxy-4-<(benzoyloxy)methyl>cyclopentanemethanol 
• 95463-56-2 (+)-1-<(1R,3S,4R)-3-hydroxy-4-(hydroxymethyl)cyclopentyl>-5-<(E)-2-bromovinyl>-1H,3H-pyrimidine-2,4-dione 
• 120905-33-1 (+)-(1R,3S,4R)-3-acetoxy-4-<(benzoyloxy)methyl>cyclopentanecarboxylic acid 
• 120905-34-2 (+)-(1R,3S,4R)-N-<3-acetoxy-4-<(benzoyloxy)methyl>cyclopentyl>urea 
• 120905-35-3 (+)-3-ethoxy-N-cyclopentyl>carbamoyl>propenamide 

Relevant academic research and scientific papers

Synthesis and Antiviral Activity of the Enantiomeric Forms of Carba-5-iodo-2'-deoxyuridine and Carba-(E)-5-(2-bromovinyl)-2'-deoxyuridine

Both enantiomers of the carbocyclic analogues of 5-iodo-2'-deoxyuridine (14 and ent-14) and of (E)-5-(2-bromovinyl)-2'-deoxyuridine (16 and ent-16) were synthesized by using (+)- or (-)-endo-norborn-5-en-2-yl acetate or butyrate, respectively, as starting