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A Simple and Convenient Copper-Catalyzed Tandem Synthesis of Quinoline-2-carboxylates at Room Temperature.

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TLDR
In this paper, a simple and convenient copper-catalyzed method for the synthesis of quinoline-2-carboxylate derivatives through sequential intermolecular addition of alkynes onto imines and subsequent intramolecular ring closure by arylation was developed.
Abstract
We developed a simple and convenient copper-catalyzed method for the synthesis of quinoline-2-carboxylate derivatives through sequential intermolecular addition of alkynes onto imines and subsequent intramolecular ring closure by arylation. The efficiency of this system allowed the reactions to be carried out at room temperature.

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A review on transition-metal mediated synthesis of quinolines

TL;DR: A systematic and comprehensive literature survey on the transition metal catalyzed synthesis of polysubstituted quinolines can be found in this paper, where the authors provide an overview of the literature available on transition-metal catalyzed synthetic methodologies for the synthesis of quinoline derivatives.
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Journal ArticleDOI

A Simple and Convenient Copper-Catalyzed Tandem Synthesis of Quinoline-2-carboxylates at Room Temperature

TL;DR: A simple and convenient copper-catalyzed method for the synthesis of quinoline-2-carboxylate derivatives through sequential intermolecular addition of alkynes onto imines and subsequent intramolecular ring closure by arylation is developed.
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