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Pd(OAc)(2)-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones

An intramolecular dehydrogenative C–H activation enabled an efficient synthesis of an uracil-annulated β-carbolinone ring system. The reaction is simple, efficient and high yielding (85–92%).

Detalles Bibliográficos
Autores principales: Mondal, Biplab, Hazra, Somjit, Panda, Tarun K, Roy, Brindaban
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578345/
https://www.ncbi.nlm.nih.gov/pubmed/26425190
http://dx.doi.org/10.3762/bjoc.11.146
Descripción
Sumario:An intramolecular dehydrogenative C–H activation enabled an efficient synthesis of an uracil-annulated β-carbolinone ring system. The reaction is simple, efficient and high yielding (85–92%).