Sulfonic acid functionalized pyridinium chloride [pyridine-SO3 H]Cl has been synthesized as a novel Brnsted acidic ionic liquid and characterized on the basis of its FT-IR,1H and 13C NMR,MS,ther-mogravimetry,and deriv...Sulfonic acid functionalized pyridinium chloride [pyridine-SO3 H]Cl has been synthesized as a novel Brnsted acidic ionic liquid and characterized on the basis of its FT-IR,1H and 13C NMR,MS,ther-mogravimetry,and derivative thermogravimetry data.The material has also been used as a highly efficient,homogeneous,and reusable catalyst for the preparation of hexahydroquinolines according to the one-pot multi-component condensation of arylaldehydes,dimedone(5,5-dimethylcyclohexane-1,3-dione),β-ketoesters,and ammonium acetate under solvent-free conditions.展开更多
An efficient solvent‐free protocol for the synthesis of 14‐aryl‐14H‐dibenzo[a,j]xanthenes from the condensation of 2‐naphthol with arylaldehydes, using acetic acid functionalized imidazolium salts (1‐carboxymet...An efficient solvent‐free protocol for the synthesis of 14‐aryl‐14H‐dibenzo[a,j]xanthenes from the condensation of 2‐naphthol with arylaldehydes, using acetic acid functionalized imidazolium salts (1‐carboxymethyl‐3‐methylimidazolium bromide ([cmmim]Br) and 1‐carboxymethy1‐3-me-thylimidazolium tetrafluoroborate([cmmim]BF4) as reusable catalysts, has been developed. The turn over frequency on the catalysts is several times higher than the other previously reported catalysts. Also, thermal gravimetric analysis and powder X‐ray diffraction pattern of the catalysts have been studied.展开更多
A Pd-catalyzed enantioselective synthesis of 2-methyl-3-methyleneindoline in up to 89% yield and 84% ee from racemic vinyl benzoxazinanones has been developed with the help of(R,R)-BenzP*ligand.Mechanism studies suppo...A Pd-catalyzed enantioselective synthesis of 2-methyl-3-methyleneindoline in up to 89% yield and 84% ee from racemic vinyl benzoxazinanones has been developed with the help of(R,R)-BenzP*ligand.Mechanism studies support the formation of palladacyclobutane as the key intermediate via C2 attack to π-allyl Pd complex.The β-hydride elimination provides a new reaction pathway for the palladacyclobutane.展开更多
基金partial support for this work from the Research Affairs Office of Sayyed Jamaleddin Asadabadi University,Bu-Ali Sina University(Grant no. 32-1716 entitled development of chemical methods,reagents and molecules)the Center of Excellence in Development of Chemical Method(CEDCM),Hamedan,I.R. Iran
文摘Sulfonic acid functionalized pyridinium chloride [pyridine-SO3 H]Cl has been synthesized as a novel Brnsted acidic ionic liquid and characterized on the basis of its FT-IR,1H and 13C NMR,MS,ther-mogravimetry,and derivative thermogravimetry data.The material has also been used as a highly efficient,homogeneous,and reusable catalyst for the preparation of hexahydroquinolines according to the one-pot multi-component condensation of arylaldehydes,dimedone(5,5-dimethylcyclohexane-1,3-dione),β-ketoesters,and ammonium acetate under solvent-free conditions.
基金Bu-Ali Sina University and University of Sayyed Jamaleddin Asadabadi, Asadabad
文摘An efficient solvent‐free protocol for the synthesis of 14‐aryl‐14H‐dibenzo[a,j]xanthenes from the condensation of 2‐naphthol with arylaldehydes, using acetic acid functionalized imidazolium salts (1‐carboxymethyl‐3‐methylimidazolium bromide ([cmmim]Br) and 1‐carboxymethy1‐3-me-thylimidazolium tetrafluoroborate([cmmim]BF4) as reusable catalysts, has been developed. The turn over frequency on the catalysts is several times higher than the other previously reported catalysts. Also, thermal gravimetric analysis and powder X‐ray diffraction pattern of the catalysts have been studied.
基金supported by National Natural Science Foundation of China(NSFC,No.21602130)Shanghai Jiao Tong University。
文摘A Pd-catalyzed enantioselective synthesis of 2-methyl-3-methyleneindoline in up to 89% yield and 84% ee from racemic vinyl benzoxazinanones has been developed with the help of(R,R)-BenzP*ligand.Mechanism studies support the formation of palladacyclobutane as the key intermediate via C2 attack to π-allyl Pd complex.The β-hydride elimination provides a new reaction pathway for the palladacyclobutane.
