Synthesis of 2,4-Disubstituted Quinolines by the Reaction of Propargylic Alcohols with Anilines in a Polyphosphoric Acid Medium

Synthesis of 2,4-Disubstituted Quinolines by the Reaction of Propargylic Alcohols with Anilines in a Polyphosphoric Acid Medium

A novel method for quinoline synthesis based on the interaction of propargylic alcohols with anilines in the presence of polyphosphoric acid (PPA) has been developed. It has been discovered that propargylic alcohols in a PPA medium are capable of hydrolyzing into chalcones. The use of PPA in ethyl a...

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Detalles Bibliográficos
Autores principales:	Aksenov, A. V., Аксенов, А. В., Aksenov, N. A., Аксенов, Н. А., Akulova, A. S., Акулова, А. С., Makieva, D. C., Макиева, Д. С., Aksenova, I. V., Аксенова, И. В., Arutiunov, N. A., Арутюнов, Н. А., Aksenov, D. A., Аксенов, Д. А.
Formato:	Статья
Lenguaje:	English
Publicado:	Pleiades Publishing 2025
Materias:	Acetylenes The Friedel-crafts reaction Heterocyclization Kucherov reaction Propargyl alcohols Quinolines
Acceso en línea:	https://dspace.ncfu.ru/handle/123456789/31842
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

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