Cargando…
Alkene Isomerization Revitalizes the Coates–Claisen Rearrangement
The [3,3]‐sigmatropic rearrangement of allylic vinyl acetals, first investigated by Coates nearly four decades ago, is set apart from other variants of the Claisen rearrangement owing to the versatile monoprotected 1,5‐dicarbonyl motif featured in the products. Unfortunately, the synthetically elusi...
Autores principales: | Massad, Itai, Marek, Ilan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456971/ https://www.ncbi.nlm.nih.gov/pubmed/34133046 http://dx.doi.org/10.1002/anie.202105834 |
Ejemplares similares
-
Stereoselective tandem iridium-catalyzed alkene isomerization-cope rearrangement of ω-diene epoxides: efficient access to acyclic 1,6-dicarbonyl compounds
por: Suresh, Rahul, et al.
Publicado: (2021) -
Stereodivergent Access to Trisubstituted Alkenylboronate
Esters through Alkene Isomerization
por: Segura, Lucas, et al.
Publicado: (2021) -
Claisen thermally rearranged (CTR) polymers
por: Tena, Alberto, et al.
Publicado: (2016) -
Microwave Accelerated Aza-Claisen Rearrangement
por: Gajdošíková, Eva, et al.
Publicado: (2008) -
Recent Developments in the Reformatsky-Claisen Rearrangement
por: Ishihara, Jun, et al.
Publicado: (2012)