Reactivity and selectivity of charged phenyl radicals toward amino acids in a fourier transform ion cyclotron resonance mass spectrometer

Journal of the American Chemical Society

Volumn 133, Issue 24, 2011, Pages 9331-9342

  Pates, George O ^a   Guler, Leonard ^a   Nash, John J ^a   Kenttämaa, Hilkka I ^a  

^a PURDUE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION-ELIMINATION; AMINO TERMINUS; ELECTROPHILICITY; FOURIER TRANSFORM ION CYCLOTRON RESONANCE MASS SPECTROMETERS; GASPHASE; HYDROGEN ATOM ABSTRACTION; HYDROGEN ATOMS; IONIZATION ENERGIES; PHENYL RADICALS; PYRIDINIUM; QUANTUM CHEMICAL CALCULATIONS; RADICAL MECHANISM; RADICAL SITES; REACTION EFFICIENCY; REACTION MECHANISM; REACTION PATHWAYS; SIDE-CHAINS; VERTICAL ELECTRON AFFINITIES;

ABSTRACTING; ADDITION REACTIONS; AMINO ACIDS; ATOMS; CYCLOTRONS; DEUTERIUM; ELECTRON CYCLOTRON RESONANCE; HYDROGEN; IONIZATION OF GASES; MASS SPECTROMETERS; MASS SPECTROMETRY; QUANTUM CHEMISTRY; RESONANCE;

FOURIER TRANSFORMS;

ALANINE; AMINO ACID; CYSTEINE; DEUTERIUM; GLYCINE; HYDROGEN; ISOLEUCINE; LEUCINE; METHIONINE; N (3 NITRO 5 DEHYDROPHENYL)PYRIDINIUM; NITROGEN 15; PHENYL GROUP; PROLINE; RADICAL; UNCLASSIFIED DRUG; VALINE;

ADDITION REACTION; AMINO TERMINAL SEQUENCE; ARTICLE; BINDING AFFINITY; CHEMICAL STRUCTURE; ELECTRON; ELECTROPHILICITY; ELIMINATION REACTION; ION CYCLOTRON RESONANCE MASS SPECTROMETRY; IONIZATION; MASS SPECTROMETER; MOLECULAR MECHANICS; NUCLEOPHILICITY; QUANTUM CHEMISTRY; SUBSTITUTION REACTION;

AMINO ACIDS; DEUTERIUM; FOURIER ANALYSIS; FREE RADICALS; MASS SPECTROMETRY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 79959253818     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja111280t     Document Type: Article

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