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The "β-Fluorine Effect" in the Non-Metal Hydride Radical Deoxygenation of Fluorine-Containing Nucleoside Xanthates
An alternative method to conduct a Barton-McCombie deoxygenation in nucleosides is described. The utility of the procedure is limited to structures with an electronegative substituent, particularly fluorine, in the β-position relative to the radical center. The process is radical in nature and trigg...
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Published in: | Nucleosides, nucleotides & nucleic acids nucleotides & nucleic acids, 2000-01, Vol.19 (1-2), p.1-12 |
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cites | cdi_FETCH-LOGICAL-c398t-f4d9b9bc07a525aeb5655d2f133f3e3b9877280e91adf47dfc3822548f274a1a3 |
container_end_page | 12 |
container_issue | 1-2 |
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container_title | Nucleosides, nucleotides & nucleic acids |
container_volume | 19 |
creator | Siddiqui, Maqbool A. Driscoll, John S. Abushanab, Elie Kelley, James A. Barchi, Joseph J. Marquez, Victor E. |
description | An alternative method to conduct a Barton-McCombie deoxygenation in nucleosides is described. The utility of the procedure is limited to structures with an electronegative substituent, particularly fluorine, in the β-position relative to the radical center. The process is radical in nature and triggered by peroxides. The abstraction of hydrogen from the solvent is favorably influenced by the presence of a β-fluorine. |
doi_str_mv | 10.1080/15257770008032993 |
format | article |
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subjects | AIDS/HIV Anti-HIV Agents - chemical synthesis Dideoxyadenosine - analogs & derivatives Dideoxyadenosine - chemical synthesis Fluorine - chemistry Free Radicals - chemistry Hydrogen Magnetic Resonance Spectroscopy Oxidation-Reduction Stereoisomerism Structure-Activity Relationship Thiones - chemical synthesis |
title | The "β-Fluorine Effect" in the Non-Metal Hydride Radical Deoxygenation of Fluorine-Containing Nucleoside Xanthates |
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