posted on 2013-08-16, 00:00authored byRosalyn Peña, Sandra Jiménez-Alonso, Gabriela Feresin, Alejandro Tapia, Sebastián Méndez-Alvarez, Félix Machín, Ángel
G. Ravelo, Ana Estévez-Braun
A series
of dihydropyran and dihydropyridin embelin derivatives
were synthesized through a novel and straightforward one-pot protocol
based on a three-component reaction with embelin, aldehydes, and cyclic
enaminones as synthetic imputs. The type of substituent on the nitrogen
atom of the β-enaminone is key to obtain nitrogenated or oxygenated
rings. The obtained compounds were active against Gram-positive bacteria,
including multiresistant Staphylococcus aureus clinical
isolates.