位置：成果数据库 > 著作 > 著作详情页
Are allylic hydrogens in catechins more abstractable than catecholic hydrogens.
  • 所属机构名称：山东师范大学
  • 成果类型：著作
  • 出版社：J Am Oil Chem Soc, 79. 943-944, 2002 (SCI收录)
  • 语言：英文
  • 相关项目：朊病毒（prion）抗氧化与促氧化作用的分子机理
作者： Hong-Yu Zhang|Lan-Fen Wang.|
同著作项目
朊病毒（prion）抗氧化与促氧化作用的分子机理
期刊论文 4 著作 18
同项目著作
Theoretical elucidation of structure-activity relationship for coumarins to scavenge peroxyl radical.
On the effectiveness of EPR radical equilibration technique in estimating O-H bond dissociation enthalpies of catechols and other complex polyphenols.
Unexpected role of 5-OH in DPPH radical-scavenging activity of 4-thiaflavans. Revealed by theoretical calculations.
Theoretical elucidation of nitrogen dioxide radical-scavenging activity difference of hydroxycinnamic acid derivatives.
DFT calculations indicate that 1,4-dihydropyridine is a promising lead antioxidant.
A new strategy to combat Alzheimer’s disease. Combining radical-scavenging potential with metal-protein-attenuating ability in one molecule
Radical scavenging potential of phenolic compounds encountered in O. Europaea products as indicated by calculation of bond dissociation enthalpy and ionization potential values
Theoretical investigation on radical-coupling reactivity of indolinonic aminoxyls
Theoretical elucidation on structure-antioxidant activity relationships for indolinonic hydroxylamines
1,4-Pyrone effects on O-H bond dissociation energies of catechols in flavonoids: A density functional theory study
脉冲辐解研究3,4－亚甲二氧基苯甲醛的亲电性
On the O-H bond dissociation enthalpy of catechol
Why B-ring is the active center for genistein to scavenge peroxyl radical. A DFT study.
A theoretical investigation on DPPH radical-scavenging mechanism of edaravone.
Substituent effects on O-H bond dissociation enthalpies and ionization potentials of catechols: a DFT study and its implications in rational design of phenolic antioxidants and elucidation of structur
S-H proton dissociation enthalpies of thiophenolic cation radicals. A DFT study
A DFT study on intramolecular hydrogen bonds in substituted catechols and their radicals