Reference health
Kinetic isotope effects and mechanism of biomimetic oxidation of methane and benzene on FeZSM-5 zeolite
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24/24 checkable references clean · checked 2026-07-22
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
11 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 24 checked references that resolve
resolves10.1021/cr00027a011
Reactions of Non-Heme Iron(II) Centers with Dioxygen in Biology and Chemistry
resolves10.1016/S0167-2991(08)60033-6
Chapter I.4 Recent Advances in Catalytic Oxidations Relevant to Oxygenases
resolves10.1038/370541a0
An efficient mimic of cytochrome P-450 from a zeolite-encaged iron complex in a polymer membrane
resolves10.1021/ja00024a031
X-ray absorption, Moessbauer, and EPR studies of the dinuclear iron center in the hydroxylase component of methane monooxygenase
resolves10.1016/S0065-2164(08)70330-7
Oxidation of Hydrocarbons by Methane Monooxygenases from a Variety of Microbes
resolves10.1246/cl.1994.1893
Selective Oxidation of Methane to Methanol over FePO4 Using N2O and H2 at Low Temperatures
resolves10.1016/0304-5102(90)85197-P
The role of iron in N2O decomposition on ZSM-5 zeolite and reactivity of the surface oxygen formed
resolves10.1006/jcat.1993.1038
Catalytic Properties of ZSM-5 Zeolites in N2O Decomposition: The Role of Iron
resolves10.1016/0926-860X(92)80003-U
Oxidation of benzene to phenol by nitrous oxide over Fe-ZSM-5 zeolites
resolves10.1016/0926-860X(96)00055-5
On the role of Brønsted acidity in the oxidation of benzene to phenol by nitrous oxide
resolves10.1007/BF02068538
Rate of14N2 desorption from the surfaces of nitrides in the presence and absence of15N2 in the gas phase
resolves10.1016/0006-291X(77)90758-6
Intramolecular determination of primary kinetic isotope effects in hydroxylations catalyzed by cytochrome P-450
resolves10.1021/ja00015a025
A radical clock investigation of microsomal cytochrome P-450 hydroxylation of hydrocarbons. Rate of oxygen rebound
resolves10.1021/ja00056a018
Radical clock substrate probes and kinetic isotope effect studies of the hydroxylation of hydrocarbons by methane monooxygenase
resolves10.1016/S0021-9258(18)55117-6
Oxidation of deuterated compounds by high specific activity methane monooxygenase from Methylosinus trichosporium. Mechanistic implications.
resolves10.1042/bj2590167
A stopped-flow kinetic study of soluble methane mono-oxygenase from <i>Methylococcus capsulatus</i> (Bath)
resolves10.1021/bi960596w
Large Kinetic Isotope Effects in Methane Oxidation Catalyzed by Methane Monooxygenase: Evidence for C−H Bond Cleavage in a Reaction Cycle Intermediate
resolves10.1007/BF00807450
Selective oxidation of methane by dinitrogen monoxide on FeZSM-5 zeolites. Ab initio quantum chemical analysis
resolves10.1016/0014-5793(95)00195-F
The mechanism of methane and dioxygen activation in the catalytic cycle of methane monooxygenase
resolves10.1021/ar950146g
Modeling the Oxygen Activation Chemistry of Methane Monooxygenase and Ribonucleotide Reductase
resolves10.1021/bi00680a033
Deuterium isotope effects during formation of phenols by hepatic monoxygenases. Evidence for an alternative to the arene oxide pathway
The 11 references without a DOI — listed, not checked
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB1
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB5
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB6
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB11
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB14
no DOI — not checkedK.A. Dubkov, V.I.Sobolev, G.I. Panov, Kinet. Katal., submitted for publication.
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB24
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB27
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB30
no DOI — not checked10.1016/S1381-1169(97)00051-4_BIB34
no DOI — not checkedBiotransformations in Organic Chemistry
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