A novel, efficient, and mild synthetic route for the preparation of 2-aminoquinolines via a gold-catalyzed cascade reaction of β-(2-aminophenyl)-α,β-ynones with ynamides has been developed. This process tolerates a wide range of functionalities such as halogen, alkyl, aryl, and heteroaryl groups, leading to original heterocycles in fair to very good yields.

Gold-Catalyzed Cascade Reaction of β‑(2-Aminophenyl)-α,β-ynones with Ynamides: A Sequential Route to Polysubstituted 2‑Aminoquinolines

Navnath D. Rode
Membro del Collaboration Group
;
Antonio Arcadi
;
Antonella Di Nicola
Membro del Collaboration Group
;
Fabio Marinelli
Membro del Collaboration Group
;
2018-01-01

Abstract

A novel, efficient, and mild synthetic route for the preparation of 2-aminoquinolines via a gold-catalyzed cascade reaction of β-(2-aminophenyl)-α,β-ynones with ynamides has been developed. This process tolerates a wide range of functionalities such as halogen, alkyl, aryl, and heteroaryl groups, leading to original heterocycles in fair to very good yields.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/126941
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