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Volumn 112, Issue 16, 2008, Pages 5209-5217

One-electron reduction of 8-bromo-2-aminoadenosine in the aqueous phase: Radiation chemical and DFT studies of the mechanism

Author keywords

[No Author keywords available]

Indexed keywords

AQUEOUS PHASE; HYDRATED ELECTRONS; ONE ELECTRON REDUCTIONS; TAUTOMERIC FORMS;

EID: 45549109256     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp800480f     Document Type: Article
Times cited : (8)

References (35)
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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.
    • 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.
    • 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.
  • 18
    • 84906385232 scopus 로고    scopus 로고
    • 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.
    • 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.
  • 19
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    • Analogous results were observed for 8-bromoguanosine.5
    • 5
  • 20
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    • -1, see: Hug, G. L. Natl. Stand. Ref. Data Ser. (U.S., Natl. Bur. Stand.) 1981, No. 69.
    • -1, see: Hug, G. L. Natl. Stand. Ref. Data Ser. (U.S., Natl. Bur. Stand.) 1981, No. 69.
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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
    • 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).
    • 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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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.