Azolyacetones as Precursors to Indoles and Naphthofurans Facilitated by Microwave Irradiation with Simultaneous Cooling

Phthalimide reacted with phenacyl bromide under microwave irradiation to yield phenacyl isoindolidene-1,3-dione (3b), while 3a reacted with phenylhydrazine to yield the phenylhydrazone 4 that was readily converted into indoylphthalimide 8. Similarly N-benzotriazolylacetone (6a) reacted with phenyl h...

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Detalles Bibliográficos
Autores principales: Al-Mousawi, Saleh Mohammed, El-Apasery, Morsy Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255476/
https://www.ncbi.nlm.nih.gov/pubmed/19701139
http://dx.doi.org/10.3390/molecules14082976

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255476/
https://www.ncbi.nlm.nih.gov/pubmed/19701139
http://dx.doi.org/10.3390/molecules14082976

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