Cyclization of Free Radicals at the C-7 Position of Ethyl Indole–2-carboxylate Derivatives: an Entry to a New Class of Duocarmycin Analogues

Aryl free-radicals generated at the C-7 position of ethyl indole-2-carboxylates bearing N-allyl and propargylic groups triggered intramolecular cyclizations to furnish a new class of Duocarmycin analogues, formal ethyl pyrrolo[3,2,1-ij]quinoline-2-carboxylate derivatives, through the less favorable...

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Detalles Bibliográficos
Autores principales: Al-Said, Naim H., Shawakfeh, Khaled Q., Abdullah, Wasim N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2005
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147633/
https://www.ncbi.nlm.nih.gov/pubmed/18007541
http://dx.doi.org/10.3390/10121446

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147633/
https://www.ncbi.nlm.nih.gov/pubmed/18007541
http://dx.doi.org/10.3390/10121446

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