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Antioxidant Motifs in Flavonoids: O–H versus C–H Bond Dissociation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/chem.200305311openalex-snapshot
A Critical Evaluation of the Factors Determining the Effect of Intramolecular Hydrogen Bonding on the OH Bond Dissociation Enthalpy of Catechol and of Flavonoid Antioxidants
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inferredcites →https://doi.org/10.1007/s00253-011-3449-2openalex-snapshot
Metabolic engineering of flavonoids in plants and microorganisms
inferredcites →https://doi.org/10.1007/s10086-005-0780-1openalex-snapshot
Knotwood and bark extracts: strong antioxidants from waste materials
inferredcites →https://doi.org/10.1016/0095-8522(49)90023-9openalex-snapshot
Diffusion-controlled reaction rates
inferredcites →https://doi.org/10.1016/0891-5849(95)02227-9openalex-snapshot
Structure-antioxidant activity relationships of flavonoids and phenolic acids
inferredcites →https://doi.org/10.1016/j.aca.2004.05.038openalex-snapshot
Catechin electrochemical oxidation mechanisms
inferredcites →https://doi.org/10.1016/j.ajps.2017.08.004openalex-snapshot
Bioactive flavonoids in medicinal plants: Structure, activity and biological fate
inferredcites →https://doi.org/10.1016/j.bmc.2009.11.015openalex-snapshot
Reliability of bond dissociation enthalpy calculated by the PM6 method and experimental TEAC values in antiradical QSAR of flavonoids
inferredcites →https://doi.org/10.1016/j.comptc.2013.02.018openalex-snapshot
Theoretical investigation of stereochemistry and solvent influence on antioxidant activity of ferulic acid
inferredcites →https://doi.org/10.1016/j.cplett.2014.08.067openalex-snapshot
Theoretical investigation on the bond dissociation enthalpies of phenolic compounds extracted from Artocarpus altilis using ONIOM(ROB3LYP/6-311++G(2df,2p):PM6) method
inferredcites →https://doi.org/10.1016/j.cplett.2015.02.033openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.dyepig.2013.12.015openalex-snapshot
Theoretical investigation on the antioxidative activity of anthocyanidins: A DFT/B3LYP study
inferredcites →https://doi.org/10.1016/j.foodres.2013.02.023openalex-snapshot
Ascorbic acid modifies the free radical scavenging behaviour of catechin: An insight into the mechanism
inferredcites →https://doi.org/10.1016/j.jphotobiol.2018.02.006openalex-snapshot
Investigating the scavenging of reactive oxygen species by antioxidants via theoretical and experimental methods
inferredcites →https://doi.org/10.1016/j.lfs.2005.11.004openalex-snapshot
Structure–radical scavenging activity relationships of phenolic compounds from traditional Chinese medicinal plants
inferredcites →https://doi.org/10.1016/j.phytochem.2006.07.002openalex-snapshot
Structure–radical scavenging activity relationships of flavonoids
inferredcites →https://doi.org/10.1016/j.theochem.2010.04.002openalex-snapshot
Study of the solvent effect on the enthalpies of homolytic and heterolytic N–H bond cleavage in p-phenylenediamine and tetracyano-p-phenylenediamine
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Advances in flavonoid research since 1992
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inferredcites →https://doi.org/10.1016/s0955-2863(02)00208-5openalex-snapshot
Flavonoid antioxidants: chemistry, metabolism and structure-activity relationships
inferredcites →https://doi.org/10.1021/acs.jcim.8b00847openalex-snapshot
Radical Scavenging Activity of Natural-Based Cassaine Diterpenoid Amides and Amines
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Thermodynamics of the Electron and the Proton
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Current status of transition-state theory
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Antioxidant Activity of Knotwood Extractives and Phenolic Compounds of Selected Tree Species
inferredcites →https://doi.org/10.1021/jf0502698openalex-snapshot
Standardized Methods for the Determination of Antioxidant Capacity and Phenolics in Foods and Dietary Supplements
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inferredcites →https://doi.org/10.1021/jp026190copenalex-snapshot
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inferredcites →https://doi.org/10.1021/jp052793nopenalex-snapshot
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The C−H and α(C−X) Bond Dissociation Enthalpies of Toluene, C6H5-CH2X (X = F, Cl), and Their Substituted Derivatives: A DFT Study
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inferredcites →https://doi.org/10.1021/jp111210copenalex-snapshot
Proton-Coupled Electron Transfer versus Hydrogen Atom Transfer: Generation of Charge-Localized Diabatic States
inferredcites →https://doi.org/10.1021/jp953748qopenalex-snapshot
Current Status of Transition-State Theory
inferredcites →https://doi.org/10.1038/s41598-018-30860-5openalex-snapshot
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inferredcites →https://doi.org/10.1039/b416572aopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c7ob01195dopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c7ra04798copenalex-snapshot
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inferredcites →https://doi.org/10.1039/tf9353100875openalex-snapshot
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inferredcites →https://doi.org/10.1063/1.474659openalex-snapshot
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inferredcites →https://doi.org/10.1103/physrev.35.1303openalex-snapshot
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inferredcites →https://doi.org/10.1103/physrevb.37.785openalex-snapshot
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inferredcites →https://doi.org/10.1146/annurev-food-041715-033206openalex-snapshot
Food Antioxidants: Chemical Insights at the Molecular Level
inferredcites →https://doi.org/10.1515/hf.2005.067openalex-snapshot
Bioactive phenolic substances in industrially important tree species. Part 4: Identification of two new 7-hydroxy divanillyl butyrolactol lignans in some spruce, fir, and pine species
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inferred← citeshttps://doi.org/10.3389/fnagi.2021.781468openalex-snapshot
Mitoprotective Effects of a Synergistic Nutraceutical Combination: Basis for a Prevention Strategy Against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fphar.2025.1570069openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphar.2025.1648395openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphar.2026.1797738openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/antiox11050952openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/antiox8120590openalex-snapshot
Radical Scavenging Activity of Puerarin: A Theoretical Study
inferred← citeshttps://doi.org/10.3390/foods13040582openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/foods13132086openalex-snapshot
Steam Explosion Pretreatment of Polysaccharide from Hypsizygus marmoreus: Structure and Antioxidant Activity
inferred← citeshttps://doi.org/10.3390/ijms23147816openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms241713277openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms242015391openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25158334openalex-snapshot
Identification of Antioxidant Methyl Derivatives of Ortho-Carbonyl Hydroquinones That Reduce Caco-2 Cell Energetic Metabolism and Alpha-Glucosidase Activity
inferred← citeshttps://doi.org/10.3390/ijms25179263openalex-snapshot
A PLGA/Silk Fibroin Nanofibre Membrane Loaded with Natural Flavonoid Compounds Extracted from Green Cocoons for Wound Healing
inferred← citeshttps://doi.org/10.3390/ijms26062587openalex-snapshot
Investigating the Antioxidant Efficiency of Tea Flavonoid Derivatives: A Density Functional Theory Study
inferred← citeshttps://doi.org/10.3390/membranes16050179openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules25163713openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules26206251openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules27030681openalex-snapshot
Phytochemical Diversity and Antioxidant Potential of Natural Populations of Nelumbo nucifera Gaertn. throughout the Floristic Regions in Thailand
inferred← citeshttps://doi.org/10.3390/molecules28145322openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules29112627openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules29245829openalex-snapshot
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inferred← citeshttps://doi.org/10.3892/br.2024.1854openalex-snapshot
Optimization of antioxidant activity of soursop ( Annona muricata L.) leaf extract using response surface methodology
inferred← citeshttps://doi.org/10.53879/id.60.05.13378openalex-snapshot
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inferred← citeshttps://doi.org/10.5772/intechopen.101466openalex-snapshot
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inferred← citeshttps://doi.org/10.5772/intechopen.95616openalex-snapshot
Antioxidant Activity: The Presence and Impact of Hydroxyl Groups in Small Molecules of Natural and Synthetic Origin
inferred← citeshttps://doi.org/10.7324/japs.2023.92856openalex-snapshot
Identification of flavone and flavanone from ethyl acetate fraction of Caesalpinia sappan heartwood and tentative structure-activity relationship: An in vitro and in silico approach
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