Cargando…
Experimental and Theoretical Reduction Potentials of Some Biologically Active ortho-Carbonyl para-Quinones
The rational design of quinones with specific redox properties is an issue of great interest because of their applications in pharmaceutical and material sciences. In this work, the electrochemical behavior of a series of four p-quinones was studied experimentally and theoretically. The first and se...
Autores principales: | Martínez-Cifuentes, Maximiliano, Salazar, Ricardo, Ramírez-Rodríguez, Oney, Weiss-López, Boris, Araya-Maturana, Ramiro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154728/ https://www.ncbi.nlm.nih.gov/pubmed/28375183 http://dx.doi.org/10.3390/molecules22040577 |
Ejemplares similares
-
Intramolecular Hydrogen Bond in Biologically Active o-Carbonyl Hydroquinones
por: Martínez-Cifuentes, Maximiliano, et al.
Publicado: (2014) -
Assessing Parameter Suitability for the Strength Evaluation of Intramolecular Resonance Assisted Hydrogen Bonding in o-Carbonyl Hydroquinones
por: Martínez-Cifuentes, Maximiliano, et al.
Publicado: (2019) -
4-Acetyl-3,3-diethyl-5-hydroxy-2-morpholino-2,3-dihydro-1-benzofuran
por: Vega, Andrés, et al.
Publicado: (2008) -
9,10-Dihydroxy-4,4-dimethyl-5,8-dihydroanthracen-1(4H)-one
por: Ramírez-Rodríguez, Oney, et al.
Publicado: (2008) -
8,8-Diethyl-1,4,5,8-tetrahydronaphthalene-1,4,5-trione
por: Vega, Andrés, et al.
Publicado: (2009)