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

Organic & Biomolecular Chemistry
Yang BaiGuojun Deng

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.

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Citations

Jul 1, 2016·The Journal of Organic Chemistry·Rajendra S RohokaleDilip D Dhavale
Aug 8, 2018·Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry·Jean Le Bras, Jacques Muzart
Mar 23, 2019·The Journal of Organic Chemistry·Raghuram GujjarappaChandi C Malakar
Sep 22, 2021·The Journal of Organic Chemistry·Miao-Dong SuCan-Cheng Guo

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