Chemoenzymatic Stereoselective Synthesis of <i>trans</i>-Flavan-4-ols via Lipase-Catalyzed Kinetic Resolutions
Flavan-4-ols are a subclass of flavonoids that are present in complex molecules with application in the industrial sector as pigments, antioxidants, or antimitotics, among many others. The most traditional way to achieve their synthesis is from naturally abundant flavanones, asymmetric transfer hydr...
Guardado en:
Autores principales: | Martín Soto, Irene Sanz-Machín, Humberto Rodríguez-Solla, Vicente Gotor-Fernández |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
MDPI AG
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/0248bf19714140ab9e237dc11bf5b0a8 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
SYNTHESIS AND AChE INHIBITING ACTIVITY OF 2, 4 SUBSTITUTED 6-PHENYL PYRIMIDINES
por: PAZ,CRISTIAN, et al.
Publicado: (2012) -
Comparative esterification of phenylpropanoids versus hydrophenylpropanoids acids catalyzed by lipase in organic solvent media
por: Cassani,Julia, et al.
Publicado: (2007) -
Easy access to both enantiomers of 5-hydroxyequol and 3-(4-hydroxyphenyl)chroman-8-ol
por: Takahito Uemura, et al.
Publicado: (2021) -
Effect of methyl branching of C8H18 alkanes and water activity on lipase-catalyzed enantioselective esterification of ibuprofen
por: Gottemukkala,Vijay V, et al.
Publicado: (2008) -
EL CHOCOLATE, UN PLACER SALUDABLE
por: Valenzuela B,Alfonso
Publicado: (2007)