78795-25-2

Upstream product

• 116595-43-8 (+/-)-cis methyl 3-(aminocarbonyl)cyclopentanecarboxylate 
• 116940-85-3 (+/-)-cis-3-(hydroxymethyl)cyclopentanecarboxamide 
• 78795-20-7 (+/-)-cis-3-aminocyclopentanemethanol 
• 84545-00-6 (+/-)-(1S,3R)-3-(methoxycarbonyl)cyclopentanecarboxylic acid 
• 85174-63-6 (+/-)-methyl cis-3-(chloromethanoyl)cyclopentanecarboxylate 
• 876-05-1 cis-1,3-cyclopentanedicarboxylic acid 
• 6054-16-6 cis-1,3-cyclopentanedicarboxylic acid anhydride 
• 78795-19-4 (+/-)-N-<aminocarbonyl>-3-methoxy-2-methyl-2-propenamide 

Downstream Products

• 116891-16-8 (+/-)-1--5-methyl-2,4(1H,3H)-pyrimidinedione benzoate 
• 116940-94-4 Benzoic acid (1S,3R)-3-(4-chloro-5-methyl-2-oxo-2H-pyrimidin-1-yl)-cyclopentylmethyl ester 

Relevant academic research and scientific papers

Carbocyclic Analogs of Thymine Nucleosides and Related 1-Substituted Thymines

The carbocyclic analogs of thymidine (IXf), 1-β-ribofuranosylthymine (IXg), and 1-β-3'-deoxyribofuranosylthymine (IXe) were synthesized by incorporating modifications into the Shaw method of synthesizing 2,4-(1H,3H)pyrimidinediones via acryloylureas.Simpler analogs of thymine nucleosides were also prepared by this method.The carbocyclic analog of thymidine displayed modest activity against Leukemia L1210 in vivo.It differs from a compound prepared previously by a Prins reaction.