Resumen
A cascade radical cyclization process involving oxime ethers tethered to a brominated phenyl and an activated olefin moiety is described. The generated aryl radicals using tri-n-butyltin hydride react with the C{double bond, long}N bond to yield neutral alkyl-oxyaminyl radicals, which were then simultaneously captured by the activated double bond to provide heterocyclic systems with a pyrrolidinic nucleus.
| Idioma original | Inglés |
|---|---|
| Páginas (desde-hasta) | 3909-3912 |
| Número de páginas | 4 |
| Publicación | Tetrahedron Letters |
| Volumen | 47 |
| N.º | 23 |
| DOI | |
| Estado | Publicada - 05 jun. 2006 |
| Publicado de forma externa | Sí |
Huella
Profundice en los temas de investigación de 'Sequenced cyclizations involving intramolecular capture of alkyl-oxyaminyl radicals. Synthesis of heterocyclic compounds'. En conjunto forman una huella única.Citar esto
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