Cargando…
Syntheses of Highly Functionalized Spirocyclohexenes by Formal [4+2] Annulation of Arylidene Azlactones with Allenoates
A straightforward phosphine‐catalyzed formal [4+2] annulation between α‐branched allenoates and arylidene azlactones has been developed to access highly functionalized spirocyclohexenes. This cyclization favors the γ‐addition of the phosphine‐activated allenoates over a β′‐addition pathway. Detailed...
Autores principales: | Eitzinger, Andreas, Zielke, Katharina, Widhalm, Michael, Robiette, Raphaël, Waser, Mario |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114148/ https://www.ncbi.nlm.nih.gov/pubmed/30175031 http://dx.doi.org/10.1002/ajoc.201800275 |
Ejemplares similares
-
Formal (4 + 1)-Addition of Allenoates to o-Quinone Methides
por: Zielke, Katharina, et al.
Publicado: (2018) -
Enantioselective Catalytic [4+1]‐Cyclization of ortho‐Hydroxy‐para‐Quinone Methides with Allenoates
por: Zielke, Katharina, et al.
Publicado: (2019) -
Towards a General Understanding of Carbonyl‐Stabilised Ammonium Ylide‐Mediated Epoxidation Reactions
por: Novacek, Johanna, et al.
Publicado: (2016) -
Asymmetric Synthesis of 2,3‐Dihydrobenzofurans by a [4+1] Annulation Between Ammonium Ylides and In Situ Generated o‐Quinone Methides
por: Meisinger, Nicole, et al.
Publicado: (2017) -
Multicomponent synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones (azlactones) using a mechanochemical approach
por: Fahmy, Amin F. M., et al.
Publicado: (2016)