Classon et al., "New halogenation reagent systems useful for the mild one-step conversion of alcohols into iodides or bromides" J. Org. Chem. (1988) vol. 53:6126-6130. |
Cory et al., "Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture" Cancer Comm. (1991) vol. 3:207-212. |
Devivar et al., "Benzimidazole ribonucleosides: Design, synthesis, and antiviral activity of certain 2-(alkylthio)-and 2-(benzylthio)-5,6-dichloro-1-(.beta.-D-ribofuranosyl)benzimidazoles" J. Med. Chem. (1994) vol. 37:2942-2949. |
Dobrowolska et al., "Benzimidazole nucleoside analogues as inhibitors of plant (maize seedling) casein kinases" Biochim. Biophys. Acta (1991) vol. 1080:221-226. |
Egyhazi et al., "Specific inhibition of hnRNA synthesis by 5,6-dichloro-1-.beta.-D-ribofuranosylbenzimidazole. Requirement of a free 3'-hydroxyl group, but not 2'-or 5'-hydroxyls" Biochim. Biophys. Acta (1982) vol. 697:213-220. |
Goldstein, "Analysis of a single curve with graded responses" Biostatistics: An Introductory Text, MacMillan, New York (1964) pp. 156-161. |
Hanessian et al. "Design and reactivity of organiz functional groups--2-pyridylsulfonates as nucleofugal esters: Remarkably mild transformations into halides and olefins" Heterocycles (1989) vol. 2:1115-1120. |
Holy et al. "5'-0-alkyl-5-fluorouridines: Synthesis and biological activity" Collect. Czech. Chem. Commun. (1987) vol. 52:1589-1608. |
Kanazawa et al., "Studies on d-Ribose derivatives: II.. Preparation of 2,3-Di-O-acetyl-t-deoxy-5-iodo-D-ribofuranosylchloride from 5-0-trityl-D-ribose" Nippon Kagaku Zasshi, (1959) vol. 80:200-203. |
Kanazawa, "A new synthesis of 9.beta.-(5'methylthio-D-ribofuranosyl)-adenine" Chem. Abstr. (1961) vol. 55, Abst. No. 6485. |
Kazimierczuk et al., "Preparation and properties of the 5,6-and 4,6(5,7)-dinitro derivatives of benzimidazole and their 1-.beta.-D-ribofuranosides" NUcleosides and Nucleotides (1989) vol. 8:1379-1385. |
Kazimierczuk et al., "Synthesis of, and conformational studies on, 2-trifluoromethyl substituted benzimidazole ribofuranosides" Nucleosides and Nucleotides (1982) vol. 1:275-287. |
Kissman et al., "5-deoxy-5-fluoro-D-ribofuranosyl derivatives of certain purines, pyrimidines and 5,6-dimethylbenzimidazole" J. Chem. Soc. (1958) vol. 80:5559-5564. |
Kissman et al., "The synthesis of certain 5-deoxy-D-ribofuranosylpurines" J. Am. Chem. Soc. (1957) vol. 79:5534-5540. |
Montgomery et al., "Analogs of 5'-deoxy-5'(methylthio)adenosine" J. Med. Chem. (1974) vol. 17:1197-1209. |
Perrin et al., Purification of Laboratory Chemicals, (1988) 3rd Ed., Pergamon Press, New York. A title page and table of contents are enclosed herewith. |
Prichard et al., "A microtiter virus yield reduction assay for the evaluation of antiviral compounds against human cytomegalovirus and herpes simplex virus" J. Virol. Methods (1990) vol. 28:101-106. |
Prichard et al., "A Three-dimensional model to analyze drug-drug interactions" Antiviral Res. (1991) Supplement I Abstract No. 133. |
Revankar et al., "The synthesis of 2-chloro-1-(.beta.D-ribofuranosyl) benzimidazole and certain related derivatives" J. Heterocyclic Chem. (1968) vol. 5:477-483. |
Revankar et al., "The synthesis of 2-chloro-1-.beta.D-ribofuranosyl-5,6-dimethylbenzimidazole and certain related derivatives (1)" J. Heterocyclic Chem. (1968) vol. 5:615-620. |
Saluja et al. "Synthesis and antiviral activity of certain 2-substituted-5,6-dichlorobenzimidazole acyclic nucleosides" Poster #146, Division of Medicinal Chemistry, 204th American Chemical Society National Meeting, Washington D. C., Aug. 23-28, 1992. |
Shipman et al., "Antiviral activity of arabinosyladenine and arabinosylhypoxanthine in herpes simplex virus-infected KB cells: Selective inhibition of viral deoxyribonucleic acid synthesis in synchronized suspension cultures" Antimicrob. Agents Chemother. (1976) vol. 9:120-127. |
Still et al., "Rapid chromatographic technique for preparative separations with moderate resolution" J. Org. Chem. (1978) vol. 43:2923-2925. |
Tamm, "Inhibition of influenza and mumps virus multiplication by 4,5-6-(or 5,6,7-) trichloro-1-.beta.-D-ribofuranaosyl-benzimidazole" Science (1954) vol. 120:847-848. |
Turk et al., "Pyrrolo�2,3-d!pyrimidine nucleosides as inhibitors of human cytomegalovirus" Antimicro. Agents Chemother. (1987) vol. 31:544-550. |
Verheyden et al., "Halo sugar nucleosides. IV. Synthesis of some 4'5'-unsaturated pyrimidine nucleosides" J. Org. Chem. (1974) vol. 39:3573-3579. |
Vorbruggen et al., "Nucleoside synthesis with trimethylsilyl triflate and perchlorate as catalysts" Chem. Ber. (1981) vol. 114:1234-1255. |
Vorbruggen et al., "On the mechanism of nucleoside synthesis" Chem. Ber. (1981) vol. 114:1256-1268. |
Weiss et al., "The reaction of periodate with aminosugars. Anomalous overoxidations of aminofuranosides" J. Am. Med. Soc.(1959) vol. 81:4050-4054. |
Wotring et al., "Study of the cytotoxicity and metabolism of 4-amino-3-carboxamido-1-(.beta.-D-ribofuranosyl)pyrazolo�3,4-d!pyrimidine using inhibitors of adenosine kinase and adenosine deaminase" Cancer Res. (1979) vol. 39:3018-3023. |