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4
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0026574097
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Potent inhibitors for the deamination of cytosine arabinoside and 5-aza-2′-deoxycytidine by human cytidine deaminase
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Binding of pyrimidin-2-one ribonucleoside by cytidine deaminase as the transition-state analogue 3,4-dihydrouridine and the contribution of the 4-hydroxyl group to its binding affinity
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0026575027
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The decomposition of 1-(β-D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) in alkali: Mechanism and products
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4′,1′a-Methanocarbocyclic adenosine analogues as potential inhibitors of S-adenosylhomocysteine hydrolase
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(f) Jeong, L. S.; Marquez, V. E.; Yuan, C.-S.; Borchardt, R. T. 4′,1′a-Methanocarbocyclic adenosine analogues as potential inhibitors of S-adenosylhomocysteine hydrolase. Heterocycles 1995, 41, 2651-2656,
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Synthesis, conformational analysis, and biological activity of a rigid carbocyclic analogue of 2′-deoxy-aristeromycin built on a bicyclo[3.1.0]hexane template
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(g) Siddiqui, M. A.; Ford, H., Jr.; George, C.; Marquez, V. E. Synthesis, conformational analysis, and biological activity of a rigid carbocyclic analogue of 2′-deoxy-aristeromycin built on a bicyclo[3.1.0]hexane template. Nucleosides Nucleotides 1996, 15, 235-250.
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Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides?
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(1S,2R)-[(Benzyloxy)methyl]cyclopent-3-enol. A versatile synthon for the preparation of 4′,1′a-methano- And 1′,1′a-methanocarbocyclic nucleosides
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HIV-1 Reverse transcriptase can discriminate between two conformationally locked carbocyclic AZT-triphosphate analogues
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26
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Total synthesis of (-)-neplanocin A
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