Cargando…
The Cyclohexa‐2,5‐dienyl Group as a Placeholder for Hydrogen: Organocatalytic Michael Addition of an Acetaldehyde Surrogate
An aldehyde with a cyclohexa‐2,5‐dienyl group in the α‐position is introduced as a storable surrogate of highly reactive acetaldehyde. The cyclohexa‐2,5‐dienyl unit is compatible with an enantioselective Michael addition to nitroalkenes promoted by a Hayashi–Jørgensen catalyst and can be removed by...
Autores principales: | Chen, Weiqiang, Fang, Huaquan, Xie, Kaixue, Oestreich, Martin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756304/ https://www.ncbi.nlm.nih.gov/pubmed/32808731 http://dx.doi.org/10.1002/chem.202003764 |
Ejemplares similares
-
Concerted Catalysis by Nanocellulose and Proline in Organocatalytic Michael Additions
por: Ranaivoarimanana, Naliharifetra Jessica, et al.
Publicado: (2019) -
DoE‐Driven Development of an Organocatalytic Enantioselective Addition of Acetaldehyde to Nitrostyrenes in Water
por: Nori, Valeria, et al.
Publicado: (2022) -
(6E)-N-[(4Z)-2,5-Dimethyl-4-(p-tolylimino)cyclohexa-2,5-dienylidene]-4-methylaniline
por: Jian, Fang-Fang, et al.
Publicado: (2007) -
Organocatalytic Michael Addition of 1,3-Dicarbonyl Indane Compounds to Nitrostyrenes
por: Jiang, Zhen-Yu, et al.
Publicado: (2010) -
2-(Cyclohexa-1,4-dienyl)-2-(4-methoxyphenyl)-N,N-dimethylethanaminium chloride
por: Lou, Wei-Jian, et al.
Publicado: (2009)