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• W2024796875 startingPage "233" @default.
• W2024796875 abstract "Various carbocyclic nucleosides analogs of neplanocin A (such as 5-aminoimidazole-4-carboxamide riboside, uridine, 5-iodouridine, 4-thiouridine, cytidine, thymidine, 2′-deoxyguanosine, ribofuranosylthymine, a 2,2′-anhydroderivative, 2′-deoxycytidine, 2′-deoxythiouridine, and d-arabinofuranosylcytosine analogs) were synthesized from (1R, 2S, 3R)-2,3-isopropylidenedioxy-4-methoxymethyloxymethyl-4-cyclopentenylamine. The cytidine analog was found the most active in inhibiting mouse lymphoma L5178Y cells in vitro at a concentration as low as 0.8 μg/mL." @default.
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• W2024796875 date "1987-12-01" @default.
• W2024796875 modified "2023-10-03" @default.
• W2024796875 title "Enantioselective synthesis of new analogs of neplanocin A and their biological activity" @default.
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• W2024796875 doi "https://doi.org/10.1016/s0008-6215(00)90890-5" @default.
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