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.
The 43 checked references that resolve
resolves10.1093/jn/8.5.597A New Toxicant Occurring Naturally in Certain Samples of Plant Foodstuffs
resolves10.1021/ar100059gFunctional Mimics of Glutathione Peroxidase: Bioinspired Synthetic Antioxidants
resolves10.1039/C7MT00083AOrganoselenium compounds as mimics of selenoproteins and thiol modifier agents
resolves10.1021/cr900352jOrganoselenium Chemistry: Role of Intramolecular Interactions
resolves10.1021/ja00197a065Development of synthetic compounds with glutathione peroxidase activity
resolves10.1039/C5OB01665GInsights into the catalytic mechanism of synthetic glutathione peroxidase mimetics
resolves10.1002/qua.971Redox chemistry of organoselenium compounds: Ab initio and density functional theory calculations on model systems for transition states and intermediates of the redox cycle of selenoenzymes
resolves10.1039/C8CP02748JOxidation of organic diselenides and ditellurides by H
<sub>2</sub>
O
<sub>2</sub>
for bioinspired catalyst design
resolves10.1021/ja00085a040A Model Study on the Effect of an Amino Group on the Antioxidant Activity of Glutathione Peroxidase
resolves10.1002/chem.200800963A Simple and Efficient Strategy To Enhance the Antioxidant Activities of Amino‐Substituted Glutathione Peroxidase Mimics
resolves10.1016/j.tet.2012.09.020Tertiary amine-based glutathione peroxidase mimics: some insights into the role of steric and electronic effects on antioxidant activity
resolves10.1002/chem.200900818Synthesis and Structure–Activity Correlation Studies of Secondary‐ and Tertiary‐Amine‐Based Glutathione Peroxidase Mimics
resolves10.1007/BF01972806Structure-activity relationships of a series of anti-inflammatory benzisoselenazolones (BISAs)
resolves10.1021/cr000426wChemistry of Biologically Important Synthetic Organoselenium Compounds
resolves10.1021/jp076404wEffect of Substituents on the GPx-like Activity of Ebselen: Steric versus Electronic
resolves10.1021/jp105651xTheoretical Investigations on the Reaction of Monosubstituted Tertiary-Benzylamine Selenols with Hydrogen Peroxide
resolves10.1021/ol201617tEnhanced Glutathione Peroxidase Activity of Conformationally Restricted Naphthalene
<i>peri</i>
-Dichalcogenides
resolves10.1021/acsomega.2c02286Synthesis, Catalytic GPx-like Activity, and SET Reactions of Conformationally Constrained 2,7-Dialkoxy-Substituted Naphthalene-1,8-<i>peri-</i>diselenides
resolves10.1039/D1OB02153BGlutathione peroxidase mimics based on conformationally-restricted,
<i>peri</i>
-like, 4,5-disubstituted fluorene dichalcogenides
resolves10.1021/cr00088a005Intermolecular interactions from a natural bond orbital, donor-acceptor viewpoint
resolves10.1063/1.464913Density-functional thermochemistry. III. The role of exact exchange
resolves10.1021/jp0718909Multiphilic Descriptor for Chemical Reactivity and Selectivity
resolves10.1063/1.458517A simple measure of electron localization in atomic and molecular systems
resolves10.1021/jp9820774Electron Localization in Molecules and Solids: The Meaning of ELF
resolves10.1002/anie.201701486Analyzing Reaction Rates with the Distortion/Interaction‐Activation Strain Model
resolves10.1039/c2ra20591bEffect of chelate ring and rigidity on Se⋯N interactions: a computational study
resolves10.1016/j.comptc.2012.08.040Nature of the Te⋯N intramolecular interaction in organotellurium compounds. A theoretical investigation by NBO and AIM methods
resolves10.1016/j.jhazmat.2013.12.041Comparative study of E⋯N (E=Se/Te) intramolecular interactions in organochalcogen compounds using density functional theory
resolves10.1002/hc.20055Crystal structures and molecular modeling of 1,8 chalcogenide‐substituted naphthalenes
The 9 references without a DOI — listed, not checked
no DOI — not checkedOrganoselenium and organotellurium compounds containing chalcogen-oxygen bonds in organic synthesis or related processes
no DOI — not checkedref7
no DOI — not checkedOrganochalcogen peroxidase mimetics as potential drugs: A long story of a promise still unfulfilled
no DOI — not checkedref31
no DOI — not checkedref33
no DOI — not checkedref35
no DOI — not checkedref36
no DOI — not checkedDevelopment of the Colle-Salvetti correlation-energy formula into a functional of the electron density
no DOI — not checkedThe Design and Properties of Organoselenium Compounds with Glutathione Peroxidase-Like Activity
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