En este trabajo se describe la reactividad química de derivados de chalconas y dienos exo heterocíclicos, obteniéndose una serie de compuestos los cuales fueron caracterizados y rigurosamente identificados, demostrando de esta manera la conducta de estas moléculas en ambientes controlados.The synthesis of novel of 4,5,6,7-tetrahydrobenzoxazol-2-ones is herein reported. They were obtained in moderate to good yields by a highly regio- and stereoselective Diels-Alder cycloaddition of N-substituted exo-oxazolidin-2-one dienes with chalcones or bis-chalcones as dienophilesSecretaría de Investigación y Estudios Avanzados de la Universidad Autónoma del Estado de Méxic
International audienceAn efficient synthesis of deoxy-lambertellols was reported through a highly ch...
Dihydropyrazolin-5-one dienolate 2 generated by deprotonation of 2,3-dimethyl-4-formyl-1-phenylpyraz...
Abstract: Infrared irradiation promoted the Diels-Alder cycloadditions of exo-2-oxazolidinone dienes...
International audienceWe describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-...
Chalcones belong to the flavonoid family which constitutes one of the major classes of naturally occ...
Este documento es una revisión sobre el uso de las chalcones como bloques de construcción en la sínt...
A series of chalcones and their derivatives have been synthesized. Chalcones, 1-(1,3-benzodioxol-5-y...
The present study describes the synthesis of some novel arylidene cyclic chalcones 2-(4-substituted ...
The synthesis of highly substituted hydroanthraquinone derivatives with up to three stereogenic cent...
The Diels-Alder reaction of (E)-2-styrylchromones with a pyrimidine ortho-quinodimethane is reported...
AbstractA bicyclo[6.2.1]undecane model compound of the core structure of the biologically active fur...
The synthesis of highly substituted hydroanthraquinone derivatives with up to three stereogenic cent...
After prosperous domino reactions towards benzopyrans, the products were used as the starting materi...
In the first part of this work we developed four novel methodologies for the generation of nitroso d...
An efficient and diastereoselective (CDC)–Rh-catalyzed hydroalkylation of dienes with 1,3-oxazol-5(4...
International audienceAn efficient synthesis of deoxy-lambertellols was reported through a highly ch...
Dihydropyrazolin-5-one dienolate 2 generated by deprotonation of 2,3-dimethyl-4-formyl-1-phenylpyraz...
Abstract: Infrared irradiation promoted the Diels-Alder cycloadditions of exo-2-oxazolidinone dienes...
International audienceWe describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-...
Chalcones belong to the flavonoid family which constitutes one of the major classes of naturally occ...
Este documento es una revisión sobre el uso de las chalcones como bloques de construcción en la sínt...
A series of chalcones and their derivatives have been synthesized. Chalcones, 1-(1,3-benzodioxol-5-y...
The present study describes the synthesis of some novel arylidene cyclic chalcones 2-(4-substituted ...
The synthesis of highly substituted hydroanthraquinone derivatives with up to three stereogenic cent...
The Diels-Alder reaction of (E)-2-styrylchromones with a pyrimidine ortho-quinodimethane is reported...
AbstractA bicyclo[6.2.1]undecane model compound of the core structure of the biologically active fur...
The synthesis of highly substituted hydroanthraquinone derivatives with up to three stereogenic cent...
After prosperous domino reactions towards benzopyrans, the products were used as the starting materi...
In the first part of this work we developed four novel methodologies for the generation of nitroso d...
An efficient and diastereoselective (CDC)–Rh-catalyzed hydroalkylation of dienes with 1,3-oxazol-5(4...
International audienceAn efficient synthesis of deoxy-lambertellols was reported through a highly ch...
Dihydropyrazolin-5-one dienolate 2 generated by deprotonation of 2,3-dimethyl-4-formyl-1-phenylpyraz...
Abstract: Infrared irradiation promoted the Diels-Alder cycloadditions of exo-2-oxazolidinone dienes...