Issue 15, 2015

Synthesis of 2,4-diarylsubstituted-pyridines through a Ru-catalyzed four component reaction

Abstract

A ruthenium-catalyzed one-pot synthesis of 2,4-diarylsubstituted pyridines from acetophenones, ammonium acetate and DMF under an oxygen atmosphere is described. The carbon atom situated at C6 of the pyridine ring comes from the methyl group of DMF and the nitrogen atom comes from ammonium acetate.

Graphical abstract: Synthesis of 2,4-diarylsubstituted-pyridines through a Ru-catalyzed four component reaction

Supplementary files

Article information

Article type
Communication
Submitted
28 Jan 2015
Accepted
03 Mar 2015
First published
03 Mar 2015

Org. Biomol. Chem., 2015,13, 4404-4407

Synthesis of 2,4-diarylsubstituted-pyridines through a Ru-catalyzed four component reaction

Y. Bai, L. Tang, H. Huang and G. Deng, Org. Biomol. Chem., 2015, 13, 4404 DOI: 10.1039/C5OB00162E

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