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Volumn 17, Issue 10, 2006, Pages 1325-1334

Erratum (DOI:10.1016/j.jasms.2006.07.015);Reactivity of Aromatic σ,σ-Biradicals Toward Riboses

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOTRONS; DNA; FREE RADICALS; HYDROGEN; REACTION KINETICS; SPECTROMETERS;

EID: 33749000002     PISSN: 10440305     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jasms.2006.10.022     Document Type: Erratum
Times cited : (13)

References (44)
  • 1
    • 11544314893 scopus 로고    scopus 로고
    • Oxidative Strand Scission of Nucleic Acid: Routes Initiated by Hydrogen Abstraction from the Sugar Moiety
    • Pogozelski W.K., and Tullius T.D. Oxidative Strand Scission of Nucleic Acid: Routes Initiated by Hydrogen Abstraction from the Sugar Moiety. Chem. Rev 98 (1998) 1089-1107
    • (1998) Chem. Rev , vol.98 , pp. 1089-1107
    • Pogozelski, W.K.1    Tullius, T.D.2
  • 2
    • 0026045597 scopus 로고
    • Chemistry and Biology of Enediyne-cytostatic Antibiotics
    • Nicolaou K., and Dai W. Chemistry and Biology of Enediyne-cytostatic Antibiotics. Angew. Chem. Int. Ed. Engl 30 (1991) 1387-1430
    • (1991) Angew. Chem. Int. Ed. Engl , vol.30 , pp. 1387-1430
    • Nicolaou, K.1    Dai, W.2
  • 3
    • 0001590574 scopus 로고
    • Reactions of Benzenediazonium Ions with Adenine and its Derivatives
    • Chin A., Hung M.-H., and Stock L.M. Reactions of Benzenediazonium Ions with Adenine and its Derivatives. J. Org. Chem 46 (1981) 2203-2207
    • (1981) J. Org. Chem , vol.46 , pp. 2203-2207
    • Chin, A.1    Hung, M.-H.2    Stock, L.M.3
  • 4
    • 0001051085 scopus 로고
    • Reactions of Benzenediazonium Ions with Guanine and its Derivatives
    • Hung M.-H., and Stock L.M. Reactions of Benzenediazonium Ions with Guanine and its Derivatives. J. Org. Chem 47 (1982) 448-453
    • (1982) J. Org. Chem , vol.47 , pp. 448-453
    • Hung, M.-H.1    Stock, L.M.2
  • 5
    • 0032587901 scopus 로고    scopus 로고
    • C8-Arylguanine and C8-Aryladenine Formation in Calf Thymus DNA from Arenediazonium Ions
    • Gannett P.M., Powell H.H., Rao R., Shi X., Lawson T., and Kolar C. C8-Arylguanine and C8-Aryladenine Formation in Calf Thymus DNA from Arenediazonium Ions. Chem. Res. Toxicol 12 (1999) 207-304
    • (1999) Chem. Res. Toxicol , vol.12 , pp. 207-304
    • Gannett, P.M.1    Powell, H.H.2    Rao, R.3    Shi, X.4    Lawson, T.5    Kolar, C.6
  • 6
    • 0037467078 scopus 로고    scopus 로고
    • Reactivity of Substituted Charged Phenyl Radicals toward Components of Nucleic Acids
    • Ramirez-Arizmendi L.E., Heidbrink J.L., Guler L., and Kenttämaa H.I. Reactivity of Substituted Charged Phenyl Radicals toward Components of Nucleic Acids. J. Am. Chem. Soc 125 (2003) 2272-2281
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 2272-2281
    • Ramirez-Arizmendi, L.E.1    Heidbrink, J.L.2    Guler, L.3    Kenttämaa, H.I.4
  • 7
    • 25144520202 scopus 로고    scopus 로고
    • Phenyl Radicals React with Dinucleoside Phosphates by Addition to Purine Bases and H-Atom Abstraction from a Sugar Moiety
    • Liu J., Petzold C.J., Ramirez-Arizmendi L.E., Perez J., and Kenttämaa H.I. Phenyl Radicals React with Dinucleoside Phosphates by Addition to Purine Bases and H-Atom Abstraction from a Sugar Moiety. J. Am. Chem. Soc 127 (2005) 12758-12759
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 12758-12759
    • Liu, J.1    Petzold, C.J.2    Ramirez-Arizmendi, L.E.3    Perez, J.4    Kenttämaa, H.I.5
  • 8
    • 0033961888 scopus 로고    scopus 로고
    • Polar Effects on Iodine Atom Abstraction by Charged Phenyl Radicals
    • Heidbrink J.L., Thoen K.K., and Kenttämaa H.I. Polar Effects on Iodine Atom Abstraction by Charged Phenyl Radicals. J. Org. Chem 65 (2000) 645-651
    • (2000) J. Org. Chem , vol.65 , pp. 645-651
    • Heidbrink, J.L.1    Thoen, K.K.2    Kenttämaa, H.I.3
  • 10
    • 0035917356 scopus 로고    scopus 로고
    • Polarity of the Transition State Controls the Reactivity of Related Charged Phenyl Radicals Toward Atom and Group Donors
    • Tichy S.E., Thoen K.K., Price J.M., Ferra J.J., Petucci C.J., and Kenttämaa H.I. Polarity of the Transition State Controls the Reactivity of Related Charged Phenyl Radicals Toward Atom and Group Donors. J. Org. Chem 66 (2001) 2726-2733
    • (2001) J. Org. Chem , vol.66 , pp. 2726-2733
    • Tichy, S.E.1    Thoen, K.K.2    Price, J.M.3    Ferra, J.J.4    Petucci, C.J.5    Kenttämaa, H.I.6
  • 11
    • 0030005931 scopus 로고    scopus 로고
    • Ab Initio Calculation of Hydrogen Abstraction Reactions of Phenyl Radical and p-Benzyne
    • Logan C.F., and Chen P. Ab Initio Calculation of Hydrogen Abstraction Reactions of Phenyl Radical and p-Benzyne. J. Am. Chem. Soc 118 (1996) 2113-2114
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 2113-2114
    • Logan, C.F.1    Chen, P.2
  • 15
    • 0344012205 scopus 로고    scopus 로고
    • Radical Reactions of Didehydroarenes with a 1,4-Relationship
    • Amegayibor F.S., Nash J.J., and Kenttämaa H.I. Radical Reactions of Didehydroarenes with a 1,4-Relationship. J. Am. Chem. Soc 125 (2003) 14256-14257
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 14256-14257
    • Amegayibor, F.S.1    Nash, J.J.2    Kenttämaa, H.I.3
  • 16
    • 0025858991 scopus 로고
    • Simple Method for Ion Isolation in Fourier Transform Ion Cyclotron Resonance Mass Spectrometry: Combined Notch Excitation and Selective Ion Partitioning in a Dual Cell
    • Farrell Jr. J.T., Lin P., and Kenttämaa H.I. Simple Method for Ion Isolation in Fourier Transform Ion Cyclotron Resonance Mass Spectrometry: Combined Notch Excitation and Selective Ion Partitioning in a Dual Cell. Anal. Chim. Acta 246 (1991) 227-232
    • (1991) Anal. Chim. Acta , vol.246 , pp. 227-232
    • Farrell Jr., J.T.1    Lin, P.2    Kenttämaa, H.I.3
  • 17
    • 0000709817 scopus 로고
    • Long-lived Radical Cations of Simple Organophosphates Isomerize Spontaneously to Distonic Structures in the Gas Phase
    • Zeller L., Farrell Jr. J.T., Vainiotalo P., and Kenttämaa H.I. Long-lived Radical Cations of Simple Organophosphates Isomerize Spontaneously to Distonic Structures in the Gas Phase. J. Am. Chem. Soc 114 (1992) 1205-1214
    • (1992) J. Am. Chem. Soc , vol.114 , pp. 1205-1214
    • Zeller, L.1    Farrell Jr., J.T.2    Vainiotalo, P.3    Kenttämaa, H.I.4
  • 18
    • 0012405083 scopus 로고
    • A Remarkably Stable Organic Radical Cation; the Distonic Isomer of Unstable Radical Cation of Dimethyl Propyl Phosphate
    • Kiminkinen L.K.M., Stirk K.G., and Kenttämaa H.I. A Remarkably Stable Organic Radical Cation; the Distonic Isomer of Unstable Radical Cation of Dimethyl Propyl Phosphate. J. Am. Chem. Soc 114 (1992) 2027-2031
    • (1992) J. Am. Chem. Soc , vol.114 , pp. 2027-2031
    • Kiminkinen, L.K.M.1    Stirk, K.G.2    Kenttämaa, H.I.3
  • 19
    • 0033518598 scopus 로고    scopus 로고
    • Reactivity of a Substituted m-Benzyne Biradical
    • Thoen K.K., and Kenttämaa H.I. Reactivity of a Substituted m-Benzyne Biradical. J. Am. Chem. Soc 121 (1999) 800-805
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 800-805
    • Thoen, K.K.1    Kenttämaa, H.I.2
  • 20
    • 0344808693 scopus 로고
    • Reactions of Epimeric 2,2′-Diacetyl-1,1′,2,2′-tetrahydro-1,1′-biisoqui nolines
    • Henry R.A., Nielsen A.T., and Moore D.W. Reactions of Epimeric 2,2′-Diacetyl-1,1′,2,2′-tetrahydro-1,1′-biisoqui nolines. J. Org. Chem 37 (1972) 3206-3209
    • (1972) J. Org. Chem , vol.37 , pp. 3206-3209
    • Henry, R.A.1    Nielsen, A.T.2    Moore, D.W.3
  • 21
    • 0001126815 scopus 로고
    • Bimolecular Reduction of Isoquinolines. Epimeric 1,1′,2,2′,3,3′,4,4′-Octahydro-1,1′-biisoqu inolines and Derivatives
    • Nielsen A.T. Bimolecular Reduction of Isoquinolines. Epimeric 1,1′,2,2′,3,3′,4,4′-Octahydro-1,1′-biisoqu inolines and Derivatives. J. Org. Chem 35 (1970) 2498-2503
    • (1970) J. Org. Chem , vol.35 , pp. 2498-2503
    • Nielsen, A.T.1
  • 22
    • 0010820569 scopus 로고
    • Patent, ICI, US 3930837, 1976; 3-Chloro-5-acetamidoisoquinoline as a Herbicide. U.S. patent 3,930,837, 1976
    • Serban A. Patent, ICI, US 3930837, 1976; 3-Chloro-5-acetamidoisoquinoline as a Herbicide. U.S. patent 3,930,837, 1976. Chem. Abstr 84 (1976) 180075
    • (1976) Chem. Abstr , vol.84 , pp. 180075
    • Serban, A.1
  • 23
    • 0001393328 scopus 로고
    • Halide Exchange Reactions Between Aryl Halides and Alkali Halides Catalyzed by Nickel Metal
    • Yang S.H., Li C.S., and Cheng C.H. Halide Exchange Reactions Between Aryl Halides and Alkali Halides Catalyzed by Nickel Metal. J. Org. Chem 52 (1987) 691-694
    • (1987) J. Org. Chem , vol.52 , pp. 691-694
    • Yang, S.H.1    Li, C.S.2    Cheng, C.H.3
  • 24
    • 0025780005 scopus 로고
    • Sustained Off-Resonance Irradiation for Collision-activated Dissociation Involving Fourier Transform Mass Spectrometry. Collision-Activated Dissociation Technique that Emulates Infrared Multiphoton Dissociation
    • Gauthier J.W., Trautman T.R., and Jacobson D.B. Sustained Off-Resonance Irradiation for Collision-activated Dissociation Involving Fourier Transform Mass Spectrometry. Collision-Activated Dissociation Technique that Emulates Infrared Multiphoton Dissociation. Anal. Chim. Acta 246 (1991) 211-225
    • (1991) Anal. Chim. Acta , vol.246 , pp. 211-225
    • Gauthier, J.W.1    Trautman, T.R.2    Jacobson, D.B.3
  • 25
    • 0023286029 scopus 로고
    • Phase-Modulated Stored Waveform Inverse Fourier Transform Excitation for Trapped Ion Mass Spectrometry
    • Chen L., Wang T.C.L., Ricca T.L., and Marshall A.G. Phase-Modulated Stored Waveform Inverse Fourier Transform Excitation for Trapped Ion Mass Spectrometry. Anal. Chem 59 (1987) 449-454
    • (1987) Anal. Chem , vol.59 , pp. 449-454
    • Chen, L.1    Wang, T.C.L.2    Ricca, T.L.3    Marshall, A.G.4
  • 26
    • 0020718996 scopus 로고
    • Empirical Methods for Determination of Ionization Gauge Relative Sensitivities for Different Gases
    • Bartmess J.E., and Georgiadis R.M. Empirical Methods for Determination of Ionization Gauge Relative Sensitivities for Different Gases. Vacuum 33 (1983) 149-153
    • (1983) Vacuum , vol.33 , pp. 149-153
    • Bartmess, J.E.1    Georgiadis, R.M.2
  • 27
    • 0018542686 scopus 로고
    • A New Empirical Method to Calculate Average Molecular Polarizabilities
    • Miller K.J., and Savchik J.A. A New Empirical Method to Calculate Average Molecular Polarizabilities. J. Am. Chem. Soc 101 (1979) 7206-7213
    • (1979) J. Am. Chem. Soc , vol.101 , pp. 7206-7213
    • Miller, K.J.1    Savchik, J.A.2
  • 28
    • 36749115629 scopus 로고
    • Parametrization of the Ion-polar Molecule Collision Rate Constant by Trajectory Calculations
    • Su T., and Chesnavich W.J. Parametrization of the Ion-polar Molecule Collision Rate Constant by Trajectory Calculations. J. Chem. Phys 76 (1982) 5183-5185
    • (1982) J. Chem. Phys , vol.76 , pp. 5183-5185
    • Su, T.1    Chesnavich, W.J.2
  • 29
    • 28244450969 scopus 로고    scopus 로고
    • Quantum Chemical Characterization of the Structures, Thermochemical Properties, and Singlet-Triplet Splittings of Didehydroquinolinium and Didehydroisoquinolinium Ions
    • Nash J.J., Kenttämaa H.I., and Cramer C.J. Quantum Chemical Characterization of the Structures, Thermochemical Properties, and Singlet-Triplet Splittings of Didehydroquinolinium and Didehydroisoquinolinium Ions. J. Phys. Chem. A 109 (2005) 10348-10356
    • (2005) J. Phys. Chem. A , vol.109 , pp. 10348-10356
    • Nash, J.J.1    Kenttämaa, H.I.2    Cramer, C.J.3
  • 30
    • 4143095330 scopus 로고
    • Electron Affinities of the First-row Atoms Revisited. Systematic Basis Sets and Wave Functions
    • Kendall R.A., Dunning T.H., and Harrison R.J. Electron Affinities of the First-row Atoms Revisited. Systematic Basis Sets and Wave Functions. J. Chem. Phys 96 (1992) 6796-6806
    • (1992) J. Chem. Phys , vol.96 , pp. 6796-6806
    • Kendall, R.A.1    Dunning, T.H.2    Harrison, R.J.3
  • 34
    • 0037173839 scopus 로고    scopus 로고
    • An Experimental and Computational Study of the Gas-Phase Structures of Five-Carbon Monosaccharides
    • Guler L.P., Yu Y., and Kenttämaa H.I. An Experimental and Computational Study of the Gas-Phase Structures of Five-Carbon Monosaccharides. J. Phys. Chem. A 106 (2002) 6754-6764
    • (2002) J. Phys. Chem. A , vol.106 , pp. 6754-6764
    • Guler, L.P.1    Yu, Y.2    Kenttämaa, H.I.3
  • 35
    • 33644784737 scopus 로고    scopus 로고
    • 2-Deoxyribose Radicals in the Gas Phase and Aqueous Solution. Transient Intermediates of Hydrogen Atom Abstraction from 2-Deoxyribofuranose
    • Vannier L.A., Yao C., and Turecek F. 2-Deoxyribose Radicals in the Gas Phase and Aqueous Solution. Transient Intermediates of Hydrogen Atom Abstraction from 2-Deoxyribofuranose. Collect. Czech. Chem. Commun 70 (2005) 1769-1786
    • (2005) Collect. Czech. Chem. Commun , vol.70 , pp. 1769-1786
    • Vannier, L.A.1    Yao, C.2    Turecek, F.3
  • 36
    • 0001371512 scopus 로고    scopus 로고
    • Predicting Radical-Molecule Barrier Heights: The Role of the Ionic Surface
    • Donahue N.M., Clarke J.S., and Anderson J.G. Predicting Radical-Molecule Barrier Heights: The Role of the Ionic Surface. J. Phys. Chem. A 102 (1998) 3923-3933
    • (1998) J. Phys. Chem. A , vol.102 , pp. 3923-3933
    • Donahue, N.M.1    Clarke, J.S.2    Anderson, J.G.3
  • 37
    • 0035263561 scopus 로고    scopus 로고
    • Revisiting the Hammond Postulate: The Role of Reactant and Product Ionic States in Regulating Barrier Heights, Locations, and Transition State Frequencies
    • Donahue N.M. Revisiting the Hammond Postulate: The Role of Reactant and Product Ionic States in Regulating Barrier Heights, Locations, and Transition State Frequencies. J. Phys. Chem. A 105 (2001) 1489-1497
    • (2001) J. Phys. Chem. A , vol.105 , pp. 1489-1497
    • Donahue, N.M.1
  • 38
    • 0028478535 scopus 로고
    • A Primer for Valence Bond Mixing and Avoided Crossing: General Paradigms in Chemical Reactivity
    • Shaik S. A Primer for Valence Bond Mixing and Avoided Crossing: General Paradigms in Chemical Reactivity. J. Mol. Liq 61 (1994) 49-79
    • (1994) J. Mol. Liq , vol.61 , pp. 49-79
    • Shaik, S.1
  • 39
    • 0033104833 scopus 로고    scopus 로고
    • Valence Bond Diagrams and Chemical Reactivity
    • Shaik S., and Shurki A.A. Valence Bond Diagrams and Chemical Reactivity. Angew. Chem. Int. Ed. Engl 38 (1999) 586-625
    • (1999) Angew. Chem. Int. Ed. Engl , vol.38 , pp. 586-625
    • Shaik, S.1    Shurki, A.A.2
  • 40
    • 0004032955 scopus 로고
    • Kochi J.K. (Ed), John Wiley and Sons, New York, NY
    • In: Kochi J.K. (Ed). Free Radicals Vol. 1 (1973), John Wiley and Sons, New York, NY
    • (1973) Free Radicals , vol.1
  • 42
    • 0020147079 scopus 로고
    • Which Factors Determine the Reactivity and Regioselectivity of Free Radical Substitution and Addition Reactions?
    • Tedder J.M. Which Factors Determine the Reactivity and Regioselectivity of Free Radical Substitution and Addition Reactions?. Angew. Chem. Int. Ed. Engl 21 (1982) 401-410
    • (1982) Angew. Chem. Int. Ed. Engl , vol.21 , pp. 401-410
    • Tedder, J.M.1
  • 44
    • 0001051921 scopus 로고
    • 2CN· Radicals to Substituted Alkenes: A Theoretical Study of the Reaction Mechanism
    • 2CN· Radicals to Substituted Alkenes: A Theoretical Study of the Reaction Mechanism. J. Am. Chem. Soc 116 (1994) 6284-6292
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 6284-6292
    • Wong, M.W.1    Pross, A.2    Radom, L.3


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