Reference health

Reduction of Hydrogen Peroxide by Naphthalene Peri-Diselenide-Based Glutathione Peroxidase Mimics: Mechanism and Effect of Substitutions

https://doi.org/10.2139/ssrn.4482094
CiteStamped reference-health badge
43/43 checkable references clean · checked 2026-09-08

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.

9 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 43 checked references that resolve
resolves10.1093/jn/8.5.597
A New Toxicant Occurring Naturally in Certain Samples of Plant Foodstuffs
resolves10.1007/s00128-020-03094-3
Advances in Research on the Toxicological Effects of Selenium
resolves10.1515/bchm2.1972.353.1.987
Glutathione Peroxidase, V. The kinetic mechanism
resolves10.1016/B978-0-12-152827-0.50047-5
The Glutathione Peroxidase Reaction: Molecular Basis of the Antioxidant Function of Selenium in Mammals
resolves10.1016/B978-0-12-152824-9.50015-0
Selenium–Glutathione Peroxidase: Properties and Synthesis
resolves10.1111/j.1432-1033.1983.tb07429.x
The Refined Structure of the Selenoenzyme Glutathione Peroxidase at 0.2‐nm Resolution
resolves10.1016/0006-2952(84)90083-2
A novel biologically active seleno-organic compound—1
resolves10.1016/0006-2952(84)90084-4
A novel biologically active seleno-organic compound—II
resolves10.1021/ar100059g
Functional Mimics of Glutathione Peroxidase: Bioinspired Synthetic Antioxidants
resolves10.1039/C7MT00083A
Organoselenium compounds as mimics of selenoproteins and thiol modifier agents
resolves10.1021/cr900352j
Organoselenium Chemistry: Role of Intramolecular Interactions
resolves10.1021/ja00197a065
Development of synthetic compounds with glutathione peroxidase activity
resolves10.1039/C5OB01665G
Insights into the catalytic mechanism of synthetic glutathione peroxidase mimetics
resolves10.1002/qua.971
Redox 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/C8CP02748J
Oxidation of organic diselenides and ditellurides by H <sub>2</sub> O <sub>2</sub> for bioinspired catalyst design
resolves10.1021/ja00085a040
A Model Study on the Effect of an Amino Group on the Antioxidant Activity of Glutathione Peroxidase
resolves10.1002/chem.200800963
A Simple and Efficient Strategy To Enhance the Antioxidant Activities of Amino‐Substituted Glutathione Peroxidase Mimics
resolves10.1016/j.tet.2012.09.020
Tertiary amine-based glutathione peroxidase mimics: some insights into the role of steric and electronic effects on antioxidant activity
resolves10.1002/chem.200900818
Synthesis and Structure–Activity Correlation Studies of Secondary‐ and Tertiary‐Amine‐Based Glutathione Peroxidase Mimics
resolves10.1007/BF01972806
Structure-activity relationships of a series of anti-inflammatory benzisoselenazolones (BISAs)
resolves10.1021/cr000426w
Chemistry of Biologically Important Synthetic Organoselenium Compounds
resolves10.1021/jp076404w
Effect of Substituents on the GPx-like Activity of Ebselen:  Steric versus Electronic
resolves10.1021/jp105651x
Theoretical Investigations on the Reaction of Monosubstituted Tertiary-Benzylamine Selenols with Hydrogen Peroxide
resolves10.1021/ol201617t
Enhanced Glutathione Peroxidase Activity of Conformationally Restricted Naphthalene <i>peri</i> -Dichalcogenides
resolves10.1021/acsomega.2c02286
Synthesis, Catalytic GPx-like Activity, and SET Reactions of Conformationally Constrained 2,7-Dialkoxy-Substituted Naphthalene-1,8-<i>peri-</i>diselenides
resolves10.1021/ja00443a051
Peri-bridged naphthalenes from 1,8-dilithionaphthalene
resolves10.1039/D1OB02153B
Glutathione peroxidase mimics based on conformationally-restricted, <i>peri</i> -like, 4,5-disubstituted fluorene dichalcogenides
resolves10.1021/cr00088a005
Intermolecular interactions from a natural bond orbital, donor-acceptor viewpoint
resolves10.1093/oso/9780198551683.001.0001
Atoms in Molecules
resolves10.1103/PhysRevA.38.3098
Density-functional exchange-energy approximation with correct asymptotic behavior
resolves10.1063/1.464913
Density-functional thermochemistry. III. The role of exact exchange
resolves10.1021/jp0718909
Multiphilic Descriptor for Chemical Reactivity and Selectivity
resolves10.1002/jcc.22885
Multiwfn: A multifunctional wavefunction analyzer
resolves10.1063/1.458517
A simple measure of electron localization in atomic and molecular systems
resolves10.1002/anie.199718081
ELF: The Electron Localization Function
resolves10.1021/jp9820774
Electron Localization in Molecules and Solids:  The Meaning of ELF
resolves10.1002/anie.201701486
Analyzing Reaction Rates with the Distortion/Interaction‐Activation Strain Model
resolves10.1038/s41596-019-0265-0
Understanding chemical reactivity using the activation strain model
resolves10.1039/c2ra20591b
Effect of chelate ring and rigidity on Se⋯N interactions: a computational study
resolves10.1016/j.comptc.2012.08.040
Nature of the Te⋯N intramolecular interaction in organotellurium compounds. A theoretical investigation by NBO and AIM methods
resolves10.1016/j.jhazmat.2013.12.041
Comparative study of E⋯N (E=Se/Te) intramolecular interactions in organochalcogen compounds using density functional theory
resolves10.1002/hc.20055
Crystal 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
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

checked 2026-09-08 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record

Embed this badge

Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.

<a href="https://citestamp.com/citestamped/10.2139/ssrn.4482094"><img src="https://citestamp.com/citestamped/10.2139/ssrn.4482094/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[![CiteStamped reference-health badge](https://citestamp.com/citestamped/10.2139/ssrn.4482094/badge.svg)](https://citestamp.com/citestamped/10.2139/ssrn.4482094)