Nitrogen atom insertion into indenes to access isoquinolines

We report a convenient protocol for a nitrogen atom insertion into indenes to afford isoquinolines. The reaction uses a combination of commercially available phenyliodine(iii) diacetate (PIDA) and ammonium carbamate as the nitrogen source to furnish a wide range of isoquinolines. Various substitutio...

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Detalles Bibliográficos
Autores principales: Finkelstein, Patrick, Reisenbauer, Julia C., Botlik, Bence B., Green, Ori, Florin, Andri, Morandi, Bill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016357/
https://www.ncbi.nlm.nih.gov/pubmed/36937579
http://dx.doi.org/10.1039/d2sc06952k

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016357/
https://www.ncbi.nlm.nih.gov/pubmed/36937579
http://dx.doi.org/10.1039/d2sc06952k

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