An new and efficient methodology for obtaining 2-arylpyrimidines based on the use of psulfonic acid calix[6]arene as organocatalyst is proposed. The methodology involves the formation of 1,2-dihydropyridine intermediates using a variety of aromatic aldehydes with methyl or ethyl acetoacetate and ammonium acetate, which are the same starting materials as in the Hantzsch reaction, under solvent-free reaction conditions, at 25 ºC, followed by air oxidation for 12 h. The catalyst efficiency is not compromised after its successive use in reactions. Eleven examples were obtained with very good to excellent yields of 2-arylpyridines (92%-62%). This is the first report about the use of calixarenes as catalyst in the multicomponent synthesis of 2-ar...
The application of immobilizing calixarene onto the surface of silica using a sol-gel method, as an ...
2‐Aminopyridines are key structural cores of bioactive natural products, medicinally important compo...
Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridi...
An efficient methodology for obtaining 2-arylpyrimidines based on the use of p-sulfonic acid calix[6...
AbstractA new and efficient methodology is proposed for obtaining 3,4-dihydropyrimidin-2(1H)-ones/-t...
A new and efficient methodology is proposed for obtaining 3,4-dihydropyrimidin-2(1H)-ones/-thiones t...
Wells-Dawson heteropolyacids (H6P2W18O62·24H2O) were used as catalysts in the Hantzsch-like multicom...
Se estudió la reacción multicomponente de Hantzsch para la obtención de compuestos derivados de la f...
One-pot and efficient protocol for preparation of some potent pharmaceutically valuable coumarin der...
Several supported metallo-sulphonated phthalocyanines (FePcS-NH2-SiO2, CoPcS-NH2-SiO2, and CuPcS-NH2...
A facile and environmentally benign synthesis of some 2-(2-oxo-2H-chromen-3-yl)-4-aryl-indeno[1,2-b]...
Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridi...
International audienceA multicomponent Hantzsch synthesis of 1,4-dihydropyridines and acridinediones...
A facile and simple procedure for the synthesis of novel and known calix[4]resorcinarene derivatives...
A facile, highly efficient and eco-friendly protocol for the synthesis of calix[4]pyrroles in excell...
The application of immobilizing calixarene onto the surface of silica using a sol-gel method, as an ...
2‐Aminopyridines are key structural cores of bioactive natural products, medicinally important compo...
Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridi...
An efficient methodology for obtaining 2-arylpyrimidines based on the use of p-sulfonic acid calix[6...
AbstractA new and efficient methodology is proposed for obtaining 3,4-dihydropyrimidin-2(1H)-ones/-t...
A new and efficient methodology is proposed for obtaining 3,4-dihydropyrimidin-2(1H)-ones/-thiones t...
Wells-Dawson heteropolyacids (H6P2W18O62·24H2O) were used as catalysts in the Hantzsch-like multicom...
Se estudió la reacción multicomponente de Hantzsch para la obtención de compuestos derivados de la f...
One-pot and efficient protocol for preparation of some potent pharmaceutically valuable coumarin der...
Several supported metallo-sulphonated phthalocyanines (FePcS-NH2-SiO2, CoPcS-NH2-SiO2, and CuPcS-NH2...
A facile and environmentally benign synthesis of some 2-(2-oxo-2H-chromen-3-yl)-4-aryl-indeno[1,2-b]...
Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridi...
International audienceA multicomponent Hantzsch synthesis of 1,4-dihydropyridines and acridinediones...
A facile and simple procedure for the synthesis of novel and known calix[4]resorcinarene derivatives...
A facile, highly efficient and eco-friendly protocol for the synthesis of calix[4]pyrroles in excell...
The application of immobilizing calixarene onto the surface of silica using a sol-gel method, as an ...
2‐Aminopyridines are key structural cores of bioactive natural products, medicinally important compo...
Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridi...