Artigos
URI permanente para esta coleçãohttps://locus.ufv.br/handle/123456789/11847
Navegar
2 resultados
Resultados da Pesquisa
Item Synthesis approaches to (−)-cytoxazone, a novel cytokine modulator, and related structures(Molecules, 2016-09) Diaz, Marisa A. N.; Miranda, Izabel L.; Lopes, Ítala K. B.; Diaz, Gaspar(−)-Cytoxazone, originally isolated from cultures of a Streptomyces species has an oxazolidin-2-one 4,5-disubstituted ring. It is known that this natural product presents a cytokine modulator effect through the signaling pathway of Th2 cells (type 2 cytokines), which are involved in the process of growth and differentiation of cells. From this, the interest in the development of research aimed at the total synthesis of this molecule and its analogs has remained high, which can be confirmed by the large number of publications on the topic, more than 30 to date. This review focuses on the various creative methods for the synthesis of (−)-cytoxazone and its congeners. The assessment of the preparation of this oxazolidinone and related structures serves as a treatise on the efforts made in the synthesis of this important class of compound from its first total synthesis in 1999.Item Easy access to evans’ oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivative(Molecules, 2014-06-06) Diaz, Gaspar; Freitas, Michelle A. A. de; Ricci-Silva, Maria E.; Diaz, Marisa A. N.An interesting new approach was developed for the synthesis of Evans’ chiral auxiliaries with excellent yields. In turn, another new stereoselective and efficient strategy has also allowed for the preparation of a 2-oxazolidinone derivative in 34% overall yield from the Morita-Baylis-Hillman adduct. The antibacterial activity of this oxazolidinone was tested against Staphylococcus aureus strains isolated from animals with mastitis infections.