Issue 44, 2013

Copper(ii) triflate-catalyzed reactions for the synthesis of novel and diverse quinoline carboxylates

Abstract

An efficient one-pot synthesis of a variety of quinoline carboxylates was accomplished by Cu(OTf)2-catalyzed reactions of Michael addition/cyclization/aromatization between 2-aminoaryl carbonyls and alkynyl carboxylates. This methodology offers several significant advantages, namely, ease of handling, mild reaction conditions, enhanced reaction rates, and use of an effective and non-toxic catalyst. The synthesized compounds were further transformed into highly functionalized novel quinoline carboxylates bearing aromatic rings on the quinoline skeleton using the Suzuki reaction.

Graphical abstract: Copper(ii) triflate-catalyzed reactions for the synthesis of novel and diverse quinoline carboxylates

Supplementary files

Article information

Article type
Paper
Submitted
11 Jul 2013
Accepted
13 Sep 2013
First published
30 Sep 2013

RSC Adv., 2013,3, 22039-22045

Copper(II) triflate-catalyzed reactions for the synthesis of novel and diverse quinoline carboxylates

R. P. Pandit and Y. R. Lee, RSC Adv., 2013, 3, 22039 DOI: 10.1039/C3RA44943B

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