Cargando…
Unusual mechanisms in Claisen rearrangements: an ionic fragmentation leading to a meta-selective rearrangement
A mechanistic investigation of the acid-catalysed redox-neutral oxoarylation reaction of ynamides using electrospray ionisation mass-spectrometry (ESI-MS) and quantum chemical calculations (DFT and MP2) is presented. This study reveals the diversity of pathways and products available from an otherwi...
Autores principales: | Maryasin, Boris, Kaldre, Dainis, Galaverna, Renan, Klose, Immo, Ruider, Stefan, Drescher, Martina, Kählig, Hanspeter, González, Leticia, Eberlin, Marcos N., Jurberg, Igor D., Maulide, Nuno |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941282/ https://www.ncbi.nlm.nih.gov/pubmed/29780542 http://dx.doi.org/10.1039/c7sc04736c |
Ejemplares similares
-
Inverse hydride shuttle catalysis enables the stereoselective one-step synthesis of complex frameworks
por: Klose, Immo, et al.
Publicado: (2022) -
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) -
Alkene Isomerization Revitalizes the Coates–Claisen Rearrangement
por: Massad, Itai, et al.
Publicado: (2021)