Fructose was used as an efficient catalyst for three-component condensation reactions of aryl aldehydes,malononitrile,and dimedone in a mixture of EtOH and H_2O as green solvents.The advantages of this method are a sh...Fructose was used as an efficient catalyst for three-component condensation reactions of aryl aldehydes,malononitrile,and dimedone in a mixture of EtOH and H_2O as green solvents.The advantages of this method are a short reaction time,high yields,low cost,easy accesses,and simple work-up.The mechanism of the synthesis of a derivative of 4H-tetrahydrobenzo[b]pyran was clarified using spectroscopic kinetic methods.The activation energy(Ea=65.34 kJ/mol)and related kinetic parameters(ΔG=69.14 kJ/mol,ΔS=20.99 J/(mol·K),andΔH=62.89 kJ/mol)were calculated,based on the effects of temperature,concentration,and solvent.The first step in the proposed mechanism was identified as the rate-determining step(k1),based on the steady-state approximation.展开更多
2,2'-Arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) 4l-s produced from reaction between dimedone with various aldehydes in acetonitrile using ZnO as a catalyst;whereas in the presence of ZnO-acetyl ...2,2'-Arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) 4l-s produced from reaction between dimedone with various aldehydes in acetonitrile using ZnO as a catalyst;whereas in the presence of ZnO-acetyl chloride catalysts the reaction is limited to give only 1,8-dioxo-octahydroxanthenes 3a-k in very good yields.展开更多
Saccharose was applied as an efficient and homogenous catalyst for a one-pot,three-component Mannich reaction for the formation ofβ-aminoketones from aromatic aldehydes,anilines,and acetophenone at ambient temperatur...Saccharose was applied as an efficient and homogenous catalyst for a one-pot,three-component Mannich reaction for the formation ofβ-aminoketones from aromatic aldehydes,anilines,and acetophenone at ambient temperature in excellent yields.This protocol has the following advantages: mild conditions,high yields,clean reaction profiles,operational simplicity,and environmentally benign and simple work-up procedures.展开更多
A facile one-pot synthesis of 3,4,5-substituted furan-2(5H)-one derivatives from a three-component reaction of aniline derivatives, dialkylacetylenedicarboxylates and aromatic aldehydes under mild conditions using t...A facile one-pot synthesis of 3,4,5-substituted furan-2(5H)-one derivatives from a three-component reaction of aniline derivatives, dialkylacetylenedicarboxylates and aromatic aldehydes under mild conditions using tetra-n-butylammonium bisulfate as a catalyst has been developed.展开更多
基金supported by the Research Council of the University of Sistan and Baluchestan
文摘Fructose was used as an efficient catalyst for three-component condensation reactions of aryl aldehydes,malononitrile,and dimedone in a mixture of EtOH and H_2O as green solvents.The advantages of this method are a short reaction time,high yields,low cost,easy accesses,and simple work-up.The mechanism of the synthesis of a derivative of 4H-tetrahydrobenzo[b]pyran was clarified using spectroscopic kinetic methods.The activation energy(Ea=65.34 kJ/mol)and related kinetic parameters(ΔG=69.14 kJ/mol,ΔS=20.99 J/(mol·K),andΔH=62.89 kJ/mol)were calculated,based on the effects of temperature,concentration,and solvent.The first step in the proposed mechanism was identified as the rate-determining step(k1),based on the steady-state approximation.
基金support from the Research Council of University of Sistan and Baluchestan, Iran
文摘2,2'-Arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) 4l-s produced from reaction between dimedone with various aldehydes in acetonitrile using ZnO as a catalyst;whereas in the presence of ZnO-acetyl chloride catalysts the reaction is limited to give only 1,8-dioxo-octahydroxanthenes 3a-k in very good yields.
基金financial support from the Research Council of University of Sistan and Baluchestan
文摘Saccharose was applied as an efficient and homogenous catalyst for a one-pot,three-component Mannich reaction for the formation ofβ-aminoketones from aromatic aldehydes,anilines,and acetophenone at ambient temperature in excellent yields.This protocol has the following advantages: mild conditions,high yields,clean reaction profiles,operational simplicity,and environmentally benign and simple work-up procedures.
基金fnancial support from the Research Council of the University of Sistan and Baluchestan
文摘A facile one-pot synthesis of 3,4,5-substituted furan-2(5H)-one derivatives from a three-component reaction of aniline derivatives, dialkylacetylenedicarboxylates and aromatic aldehydes under mild conditions using tetra-n-butylammonium bisulfate as a catalyst has been developed.