Issue 12, 2013

Visible-light-induced, copper(i)-catalysed C–N coupling between o-phenylenediamine and terminal alkynes: one-pot synthesis of 3-phenyl-2-hydroxy-quinoxalines

Abstract

Visible-light-initiated aerobic direct C–N coupling between o-phenylenediamines and terminal acetylenes was performed using simple copper(I) chloride as a catalyst for the synthesis of quinoxaline derivatives. The current method works well for a wide range of electron rich as well as electron poor group-substituted o-phenylenediamines and phenylacetylenes. The key component in the reaction is the direct photo-excitation of in situ generated copper arylacetylide (λabs = 420–480 nm). Moreover, as compared to the literature reports (thermal process), the current photochemical method is simple, mild, high yielding, and more viable towards the construction of biologically important quinoxaline derivatives from easily accessible raw materials, without the need of ligands and strong oxidants.

Graphical abstract: Visible-light-induced, copper(i)-catalysed C–N coupling between o-phenylenediamine and terminal alkynes: one-pot synthesis of 3-phenyl-2-hydroxy-quinoxalines

Supplementary files

Article information

Article type
Paper
Submitted
16 Jun 2013
Accepted
29 Aug 2013
First published
03 Sep 2013

Photochem. Photobiol. Sci., 2013,12, 2110-2118

Visible-light-induced, copper(I)-catalysed C–N coupling between o-phenylenediamine and terminal alkynes: one-pot synthesis of 3-phenyl-2-hydroxy-quinoxalines

A. Sagadevan, A. Ragupathi and K. C. Hwang, Photochem. Photobiol. Sci., 2013, 12, 2110 DOI: 10.1039/C3PP50186H

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