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Quantitative comparison of the actual antioxidant activity of Vitamin C, Vitamin E, and NADH

Journal of physical organic chemistry, 2022-09, Vol.35 (9), p.n/a

2022

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Thermodynamic Network Cards of Hantzsch Ester, Benzothiazoline, and Dihydrophenanthridine Releasing Two Hydrogen Atoms or Ions on 20 Elementary Steps

Journal of organic chemistry, 2020-10, Vol.85 (19), p.12535-12543

2020

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Effect of N, S atoms on the mechanisms of H‐transfer for five‐membered nitrogen‐containing heterocycles

Journal of physical organic chemistry, 2024-02, Vol.37 (2), p.n/a

2024

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A new method for determining the intrinsic resistance energy of H‐atom transfer reaction and structure–activity relationship of H‐donating ability

Journal of physical organic chemistry, 2024-02, Vol.37 (2), p.n/a

2024

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Structure–activity relationship of alkanes and alkane derivatives for the abilities of C(sp 3 )H bonds toward their H‐atom transfer reactions

Journal of physical organic chemistry, 2023-10, Vol.36 (10)

2023

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The Application of Sulfonyl Hydrazides in Electrosynthesis: A Review of Recent Studies

ACS omega, 2022-11, Vol.7 (44), p.39531-39561

2022

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Theoretical investigation on the nature of 4-substituted Hantzsch esters as alkylation agents

RSC advances, 2020-08, Vol.1 (52), p.31425-31434

2020

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Comparison of Thermodynamic, Kinetic Forces for Three NADH Analogues to Release Hydride Ion or Hydrogen Atom in Acetonitrile

ChemistrySelect (Weinheim), 2021-08, Vol.6 (31), p.8007-8010

2021

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Thermodynamic and Kinetic Studies of the Activities of Aldehydic C−H Bonds toward Their H‐Atom Transfer Reactions

ChemistrySelect (Weinheim), 2023-03, Vol.8 (9), p.n/a

2023

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Thermodynamic Evaluations of Amines as Hydrides or Two Hydrogen Ions Reductants and Imines as Protons or Two Hydrogen Ions Acceptors, as Well as Their Application in Hydrogenation Reactions

ACS omega, 2023-09, Vol.8 (35), p.31984-31997

2023

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Quantitative Estimation of the Hydrogen-Atom-Donating Ability of 4‑Substituted Hantzsch Ester Radical Cations

ACS omega, 2021-09, Vol.6 (36), p.23621-23629

2021

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Determination of Thermodynamic Affinities of Various Polar Olefins as Hydride, Hydrogen Atom, and Electron Acceptors in Acetonitrile

Journal of organic chemistry, 2013-07, Vol.78 (14), p.7154-7168

2013

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What are the differences between Hantzsch ester and H2 as two‐hydrogen‐atom donors in acetonitrile on the thermodynamics of elementary steps?

Journal of physical organic chemistry, 2017-02, Vol.30 (2), p.n/a

2017

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Comparison of Thermodynamic Energies for Elementary Steps of Anionic Hydrides to Release Hydride Ions in Acetonitrile

ChemistrySelect (Weinheim), 2022-11, Vol.7 (43), p.n/a

2022

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Evaluation of Organic Hydride/Acid Pairs as a Type of Thermodynamic-Potential-Regulated Multisite Proton-Coupled Electron Transfer Reagents

Journal of organic chemistry, 2024-05, Vol.89 (9), p.6205-6221

2024

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Thermodynamic, kinetic, and mechanistic examination of 1,5‐ dihydro‐3,4‐dihydroxy‐2‐pyrrolone derivatives as a new type of antioxidants to mimic vitamin C

Journal of physical organic chemistry, 2017-08, Vol.30 (8), p.n/a

2017

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Thermodynamic evaluations of the acceptorless dehydrogenation and hydrogenation of pre-aromatic and aromatic N-heterocycles in acetonitrile

RSC advances, 2024-01, Vol.14 (1), p.222-232

2024

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Theoretical study for evaluating and discovering organic hydride compounds as novel trifluoromethylation reagents

Organic & biomolecular chemistry, 2022-04, Vol.2 (14), p.2831-2842

2022

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Evaluation and comparison of antioxidant abilities of five bioactive molecules with C-H and O-H bonds in thermodynamics and kinetics

RSC advances, 2022-09, Vol.12 (42), p.27389-27395

2022

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Quantitative evaluation of H-donating abilities of C(sp)-H bonds of nitrogen-containing heterocycles in hydrogen atom transfer reaction

RSC advances, 2023-05, Vol.13 (23), p.1623-1633

2023

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Establishing the Thermodynamic Cards of Dipine Models' Oxidative Metabolism on 21 Potential Elementary Steps

Molecules (Basel, Switzerland), 2024-08, Vol.29 (15), p.3706

2024

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Realization of Quantitative Estimation for Reaction Rate Constants Using only One Physical Parameter for Each Reactant

ChemistrySelect (Weinheim), 2017-01, Vol.2 (3), p.904-925

2017

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Quantitative evaluation of the actual hydrogen atom donating activities of O-H bonds in phenols: structure-activity relationship

RSC advances, 2023-01, Vol.13 (5), p.3295-335

2023

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Prediction of Kinetic Isotope Effects for Various Hydride Transfer Reactions Using a New Kinetic Model

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2016-03, Vol.120 (11), p.1779-1799

2016

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Thermodynamics of various F420 coenzyme models as sources of electrons, hydride ions, hydrogen atoms and protons in acetonitrile

Organic & biomolecular chemistry, 2015-06, Vol.13 (22), p.6255-6268

2015

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Quantitative comparison of the actual antioxidant activity of Vitamin C, Vitamin E, and NADH

Thermodynamic Network Cards of Hantzsch Ester, Benzothiazoline, and Dihydrophenanthridine Releasing Two Hydrogen Atoms or Ions on 20 Elementary Steps

Effect of N, S atoms on the mechanisms of H‐transfer for five‐membered nitrogen‐containing heterocycles

A new method for determining the intrinsic resistance energy of H‐atom transfer reaction and structure–activity relationship of H‐donating ability

Structure–activity relationship of alkanes and alkane derivatives for the abilities of C(sp 3 )H bonds toward their H‐atom transfer reactions

The Application of Sulfonyl Hydrazides in Electrosynthesis: A Review of Recent Studies

Theoretical investigation on the nature of 4-substituted Hantzsch esters as alkylation agents

Comparison of Thermodynamic, Kinetic Forces for Three NADH Analogues to Release Hydride Ion or Hydrogen Atom in Acetonitrile

Thermodynamic and Kinetic Studies of the Activities of Aldehydic C−H Bonds toward Their H‐Atom Transfer Reactions

Thermodynamic Evaluations of Amines as Hydrides or Two Hydrogen Ions Reductants and Imines as Protons or Two Hydrogen Ions Acceptors, as Well as Their Application in Hydrogenation Reactions

Quantitative Estimation of the Hydrogen-Atom-Donating Ability of 4‑Substituted Hantzsch Ester Radical Cations

Determination of Thermodynamic Affinities of Various Polar Olefins as Hydride, Hydrogen Atom, and Electron Acceptors in Acetonitrile

What are the differences between Hantzsch ester and H2 as two‐hydrogen‐atom donors in acetonitrile on the thermodynamics of elementary steps?

Comparison of Thermodynamic Energies for Elementary Steps of Anionic Hydrides to Release Hydride Ions in Acetonitrile

Evaluation of Organic Hydride/Acid Pairs as a Type of Thermodynamic-Potential-Regulated Multisite Proton-Coupled Electron Transfer Reagents

Thermodynamic, kinetic, and mechanistic examination of 1,5‐ dihydro‐3,4‐dihydroxy‐2‐pyrrolone derivatives as a new type of antioxidants to mimic vitamin C

Thermodynamic evaluations of the acceptorless dehydrogenation and hydrogenation of pre-aromatic and aromatic N-heterocycles in acetonitrile

Theoretical study for evaluating and discovering organic hydride compounds as novel trifluoromethylation reagents

Evaluation and comparison of antioxidant abilities of five bioactive molecules with C-H and O-H bonds in thermodynamics and kinetics

Quantitative evaluation of H-donating abilities of C(sp)-H bonds of nitrogen-containing heterocycles in hydrogen atom transfer reaction

Establishing the Thermodynamic Cards of Dipine Models' Oxidative Metabolism on 21 Potential Elementary Steps

Realization of Quantitative Estimation for Reaction Rate Constants Using only One Physical Parameter for Each Reactant

Quantitative evaluation of the actual hydrogen atom donating activities of O-H bonds in phenols: structure-activity relationship

Prediction of Kinetic Isotope Effects for Various Hydride Transfer Reactions Using a New Kinetic Model

Thermodynamics of various F420 coenzyme models as sources of electrons, hydride ions, hydrogen atoms and protons in acetonitrile

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