Gold-catalyzed formation of pyrrolo- and indolo-oxazin-1-one derivatives: The key structure of some marine natural products

Various N-propargylpyrrole and indolecarboxylic acids were efficiently converted into 3,4-dihydropyrrolo- and indolo-oxazin-1-one derivatives by a gold(III)-catalyzed cyclization reaction. Some of the products underwent TFA-catalyzed double bond isomerization and some did not. Cyclization reactions...

Descripción completa

Detalles Bibliográficos
Autores principales: Taskaya, Sultan, Menges, Nurettin, Balci, Metin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464457/
https://www.ncbi.nlm.nih.gov/pubmed/26124892
http://dx.doi.org/10.3762/bjoc.11.101

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464457/
https://www.ncbi.nlm.nih.gov/pubmed/26124892
http://dx.doi.org/10.3762/bjoc.11.101

Ejemplares similares