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A highly reactive P450 model compound I
Seth R. Bell,
John Taylor Groves
Chemistry
High Meadows Environmental Institute
Princeton Institute for the Science and Technology of Materials
Research output
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Contribution to journal
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Article
›
peer-review
148
Scopus citations
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Engineering & Materials Science
Xanthenes
100%
Hydroxylation
60%
Rate constants
41%
Cytochrome P-450 Enzyme System
41%
Porphyrins
39%
Electrospray ionization
21%
Oxidation
19%
Hydrogen
17%
Carboxylic acids
16%
Oxidation-Reduction
14%
Mass spectrometry
14%
Positive ions
13%
Isotopes
13%
Nuclear magnetic resonance
13%
Reaction rates
12%
Acids
10%
Oxygen
8%
Modulation
8%
Substrates
7%
Monitoring
6%
Medicine & Life Sciences
Xanthenes
83%
Hydroxylation
38%
meso-tetrakis(1-methyl-4-pyridiniumyl)porphyrin
28%
Porphyrins
28%
4-ethylbenzoic acid
26%
xanthydrol
24%
Kinetics
24%
Cytochrome P-450 Enzyme System
21%
ferryl iron
19%
Carbon-13 Magnetic Resonance Spectroscopy
15%
Electrospray Ionization Mass Spectrometry
15%
Proton Magnetic Resonance Spectroscopy
13%
Hydrogen
12%
Isotopes
12%
Cations
11%
Oxidation-Reduction
10%
Catalytic Domain
10%
Oxygen
7%
fluorene-4-carboxylic acid
1%
Chemical Compounds
Xanthene
59%
Cytochrome P450
31%
4-Ethylbenzoic Acid
30%
Rate Constant
29%
Porphyrin
24%
Bond Energy
16%
Kinetic Isotope Effect
16%
Redox Potential
14%
Electrospray Ionization Mass Spectrometry
14%
Oxidation Reaction
13%
Transition State
12%
13C NMR Spectroscopy
10%
Cleavage
10%
Cation
8%
Aqueous Solution
7%
Hydrogen
7%
Reaction Yield
6%
Acid
5%