info:eu-repo/semantics/article
Microwave-Assisted Organocatalytic Intramolecular Knoevenagel/Hetero Diels–Alder Reaction with O -(Arylpropynyloxy)-Salicylaldehydes: Synthesis of Polycyclic Embelin Derivatives
Fecha
2016-10Registro en:
Martín-Acosta, Pedro; Feresin, Gabriela Egly; Tapia, Alejandro; Estevez Braun, Ana; Microwave-Assisted Organocatalytic Intramolecular Knoevenagel/Hetero Diels–Alder Reaction with O -(Arylpropynyloxy)-Salicylaldehydes: Synthesis of Polycyclic Embelin Derivatives; American Chemical Society; Journal of Organic Chemistry; 81; 20; 10-2016; 9738-9756
0022-3263
CONICET Digital
CONICET
Autor
Martín-Acosta, Pedro
Feresin, Gabriela Egly
Tapia, Alejandro
Estevez Braun, Ana
Resumen
highly efficient and regioselective approach to new polycyclic embelin derivatives through a domino Knoevenagel condensation/intramolecular hetero Diels−Alder reaction using O-(arylpropynyloxy)-salicylaldehydes in the presence of ethylenediamine diacetate (EDDA) is reported. This organocatalyzed protocol is compatible toward a wide range of aryl-substituted alkynyl ethers with electron-donating and electron-withdrawing groups. When other active methylene compounds were subjected to this domino reaction the corresponding adducts were obtained in high yield.