he quantitative studies on structure and cytokinin activity of the cucumber cotyledon expansion reiationshps of 35 urea compounds were conducted using pl1ysico-chemical parameters of the substituents and regression an...he quantitative studies on structure and cytokinin activity of the cucumber cotyledon expansion reiationshps of 35 urea compounds were conducted using pl1ysico-chemical parameters of the substituents and regression analysis,The position-specific hydrophobic,steric and electronic effects of substituents are important to the activity.A certain overlap of the optimum conformation of the ureido structure over Kinetin was observed.The coplanarity is discussed.展开更多
The authors synthesized a series of novel 5-heterocycloxy-3-substituted-1-（3-trifluoromethyl）phenyl-1H- pyrazole derivatives. Herbicidal activities of the two intermediate compounds and thirteen target compounds wer...The authors synthesized a series of novel 5-heterocycloxy-3-substituted-1-（3-trifluoromethyl）phenyl-1H- pyrazole derivatives. Herbicidal activities of the two intermediate compounds and thirteen target compounds were evaluated via Brassica napus and Echinochloa crusgalli（L.） Beauv tests. Bioassay results show that some of the compounds exhibit better inhibiting activities against Brassica napus and some of the compounds exhibit bleaching activities against Echinochloa crusgalli（L.） Beauv at 100 μg/mL.展开更多
A computer-assisted retention prediction system (RPS) of fifteen O-ethyl O-aryl N-iso- propyl phosphoramidothioates (1) in reversed-phase HPLC was investigated. The system is based on the use of four physicochemical p...A computer-assisted retention prediction system (RPS) of fifteen O-ethyl O-aryl N-iso- propyl phosphoramidothioates (1) in reversed-phase HPLC was investigated. The system is based on the use of four physicochemical parameters (hydrophobicity , electric effect σ, field effect F and steric effect ) which is closely related to the retention mechanism in reversed-phase HPLC. The system was evaluated by comparing the measured retention data with the predicted ones. The predicted values were consistent with the measured values within a relative error of 11.5%.展开更多
文摘he quantitative studies on structure and cytokinin activity of the cucumber cotyledon expansion reiationshps of 35 urea compounds were conducted using pl1ysico-chemical parameters of the substituents and regression analysis,The position-specific hydrophobic,steric and electronic effects of substituents are important to the activity.A certain overlap of the optimum conformation of the ureido structure over Kinetin was observed.The coplanarity is discussed.
基金Support by the National Natural Science Foundation of China(Nos.21002054, 20572054)the Research Fund for the Doctoral Programme of Higher Education of China(No.20100031120016)the Fundamental Research Funds for the Central Universities of China
文摘The authors synthesized a series of novel 5-heterocycloxy-3-substituted-1-（3-trifluoromethyl）phenyl-1H- pyrazole derivatives. Herbicidal activities of the two intermediate compounds and thirteen target compounds were evaluated via Brassica napus and Echinochloa crusgalli（L.） Beauv tests. Bioassay results show that some of the compounds exhibit better inhibiting activities against Brassica napus and some of the compounds exhibit bleaching activities against Echinochloa crusgalli（L.） Beauv at 100 μg/mL.
文摘A computer-assisted retention prediction system (RPS) of fifteen O-ethyl O-aryl N-iso- propyl phosphoramidothioates (1) in reversed-phase HPLC was investigated. The system is based on the use of four physicochemical parameters (hydrophobicity , electric effect σ, field effect F and steric effect ) which is closely related to the retention mechanism in reversed-phase HPLC. The system was evaluated by comparing the measured retention data with the predicted ones. The predicted values were consistent with the measured values within a relative error of 11.5%.
