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A variety of substituted 2-aminoadenosine have been synthesized and tested to establish structure-activity relationship. For example, see: Bressi, J. C.; Choe, J.; Hough, M. T.; Buckner, F. S.; Van Voorhis, W. C.; Verlinde, C. L. M. J.; Hol, W. G. J.; Gelb, M. H. J. Med. Chem. 2000, 43, 4135.
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A variety of substituted 2-aminoadenosine have been synthesized and tested to establish structure-activity relationship. For example, see: Bressi, J. C.; Choe, J.; Hough, M. T.; Buckner, F. S.; Van Voorhis, W. C.; Verlinde, C. L. M. J.; Hol, W. G. J.; Gelb, M. H. J. Med. Chem. 2000, 43, 4135.
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One-electron reduction and oxidation of 2-aminopurine in the aqueous phase by using pulse radiolysis has recently been reported, see: (a) Reynisson, J.; Steenken, S. Phys. Chem. Chem. Phys. 2005, 7, 659.
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One-electron reduction and oxidation of 2-aminopurine in the aqueous phase by using pulse radiolysis has recently been reported, see: (a) Reynisson, J.; Steenken, S. Phys. Chem. Chem. Phys. 2005, 7, 659.
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Ross, A. B.; Mallard, W. G.; Helman, W. P.; Buxton, G. V.; Huie, R. E.; Neta, P. NDRL-NIST Solution Kinetic Database, version 3; Notre Dame Radiation Laboratory: Notre Dame, IN and NIST Standard Reference Data: Gaithersburg, MD, 1998.
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84906413895
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Analogous results were observed for 8-bromoguanosine.5
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5
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20
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84906399457
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-1, see: Hug, G. L. Natl. Stand. Ref. Data Ser. (U.S., Natl. Bur. Stand.) 1981, No. 69.
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-1, see: Hug, G. L. Natl. Stand. Ref. Data Ser. (U.S., Natl. Bur. Stand.) 1981, No. 69.
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21
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This rate constant was found to be independent of the nature and concentration of the HO* scavengers t-BuOH or i-PrOH 0.1 -1.0 M, This observation ruled out the possibility that the transient decays by reacting with the alcohol, for example, by abstracting a hydrogen atom
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This rate constant was found to be independent of the nature and concentration of the HO* scavengers t-BuOH or i-PrOH (0.1 -1.0 M). This observation ruled out the possibility that the transient decays by reacting with the alcohol, for example, by abstracting a hydrogen atom.
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FACSIMILE for Windows, v. 4.0.36; MCPA Software Ltd.: U.K., 2001.
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Each of the radicals 8 and 9 has several resonance forms. The reported forms show the atoms where the spin density is expected to be highest (vide infra).
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Each of the radicals 8 and 9 has several resonance forms. The reported forms show the atoms where the spin density is expected to be highest (vide infra).
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