Cargando…
Old tricks, new dogs: organocatalytic dienamine activation of α,β-unsaturated aldehydes
Chiral secondary amines are some of the most commonly used kinds of catalysts. They have become a reliable tool for the α- and β-activation of carbonyl compounds, via HOMO, SOMO or LUMO activation pathways. Recently, chemists have turned their attention to the development of novel organocatalytic st...
Autores principales: | Marcos, Vanesa, Alemán, José |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310520/ https://www.ncbi.nlm.nih.gov/pubmed/27805198 http://dx.doi.org/10.1039/c6cs00438e |
Ejemplares similares
-
Direct β-selectivity of α,β-unsaturated γ-butyrolactam for asymmetric conjugate additions in an organocatalytic manner
por: Zhong, Yuan, et al.
Publicado: (2018) -
Asymmetric pyrone Diels–Alder reactions enabled by dienamine catalysis
por: Cole, Charles J. F., et al.
Publicado: (2019) -
Two-Carbon Homologation of Aldehydes and Ketones to α,β-Unsaturated Aldehydes
por: Petroski, Richard J., et al.
Publicado: (2011) -
Iodine/water-mediated deprotective oxidation of allylic ethers to access α,β-unsaturated ketones and aldehydes
por: Xue, Yuntian, et al.
Publicado: (2020) -
Direct access to multi-functionalized benzenes via [4 + 2] annulation of α-cyano-β-methylenones and α,β-unsaturated aldehydes
por: Jia, Qianfa, et al.
Publicado: (2020)