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1
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0023813086
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Potential inhibitors of S adenosylmethionine-dependent methyltransferases. II. Molecular dissections of neplanocin A as potential inhibitors of S-adenosylhomocysteine hydrolase
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PID: 3411600, COI: 1:CAS:528:DyaL1cXkvFemsrc%3D
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Borcherding, D. R., Narayanan, S., Hasobe, M., McKee, J. G., Keller, B. T., and Borchardt, R. T., Potential inhibitors of S adenosylmethionine-dependent methyltransferases. II. Molecular dissections of neplanocin A as potential inhibitors of S-adenosylhomocysteine hydrolase.J. Med. Chem., 31, 1729–1738 (1988). DOI: 10.1021/jm00117a011
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Borchardt, R.T.6
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0023628495
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Synthesis of analogues of neplanocin A: Utilization of optically active dihydroxycyclopentenones derived from carbohydrates
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COI: 1:CAS:528:DyaL2sXmtlOhsro%3D
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Borcherding, D. R., Scholtz, S. A., and Borchardt, R. T., Synthesis of analogues of neplanocin A: Utilization of optically active dihydroxycyclopentenones derived from carbohydrates.J. Org. Chem., 52, 5457–5461 (1987). DOI: 10.1021/jo00233a029
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Borcherding, D.R.1
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0024373015
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Synthesis and antiviral activity of the nucleotide analogue (S)-1 -[3-hydroxy-2-(phosphonylmethoxy) propyl]cytosine
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Branson, J. J., Ghazzouli, I., Hitchcock, M. J. M., Webb, R. R., and Martin, J. C., Synthesis and antiviral activity of the nucleotide analogue (S)-1 -[3-hydroxy-2-(phosphonylmethoxy) propyl]cytosine.J. Med. Chem., 32, 1457–1463 (1989). DOI: 10.1021/jm00127a010
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0019046195
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Fluorinated pyrimidine nucleosides. 4. Synthesis and antitumor testing of a series of 2′,5′-dideoxy- and 2′,3′,5′-trideoxynucleosides of 5-fluorouracil
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PID: 6447210, COI: 1:CAS:528:DyaL3cXltFCqsr0%3D
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Cook, A. F. and Holman, M. J., Fluorinated pyrimidine nucleosides. 4. Synthesis and antitumor testing of a series of 2′,5′-dideoxy- and 2′,3′,5′-trideoxynucleosides of 5-fluorouracil.J. Med. Chem., 23, 852–857 (1980). DOI: 10.1021/jm00182a008
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A new and highly effective method for the oxidation of primary and secondary alcohols to carbonyl compounds
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Corey, E. J. and Kim, C. U., A new and highly effective method for the oxidation of primary and secondary alcohols to carbonyl compounds.J. Am. Chem. Soc., 94, 7586–7587 (1972). DOI: 10.1021/ja00776a056
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Synthesis and antiviral activity of 9-[4-hydroxy-3-(hydroxymethyl) but-1-yl]purines
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PID: 3040998, COI: 1:CAS:528:DyaL2sXkvFOjt78%3D
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Harnden, M. R., Jarvest, R. L., Bacon, T. H., and Boyd M. R., Synthesis and antiviral activity of 9-[4-hydroxy-3-(hydroxymethyl) but-1-yl]purines.J. Med. Chem., 30, 1636–1642 (1987). DOI: 10.1021/jm00392a020
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Synthesis of cyclopentane analogs of 5-fluorouracil nucleosides
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Hronowski, L. J. J. and Szarek, W. A., Synthesis of cyclopentane analogs of 5-fluorouracil nucleosides.Can. J. Chem., 70, 1162–1169 (1992). DOI: 10.1139/v92-152
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Cyclopentenylcytosine. A carbocyclic nucleoside with antitumor and antiviral properties
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PID: 3411597, COI: 1:CAS:528:DyaL1cXlt12mtbo%3D
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Marquez, V. E., Lim, M.-l., Treanor, S. P., Plowman, J., Priest, M. A., Markovac, A., Khan M. S., Kaskar, B., and Driscoll, J. S., Cyclopentenylcytosine. A carbocyclic nucleoside with antitumor and antiviral properties.J. Med. Chem., 31, 1687–1694 (1988). DOI: 10.1021/jm00117a004
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Khan, M.S.7
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10
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0002137237
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Uracil analogues of the acyclonucleoside 9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]guanine(BIOLF-62)
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Unsaturated and carbocyclic nucleoside analogues: synthesis, antitumor, and antiviral activity
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PID: 1992143, COI: 1:CAS:528:DyaK3MXot1eksQ%3D%3D
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Phadtare, S., Kessel, D., Corbett, T. H., Renis, H. E., Court, B. A., and Zemlicka, J., Unsaturated and carbocyclic nucleoside analogues: synthesis, antitumor, and antiviral activity.J. Med. Chem., 34, 421–429 (1991). DOI: 10.1021/jm00105a064
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