Issue 58, 2015

KOtBu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones

Abstract

The KOtBu-mediated annulation of acetonitrile with aldehyde was observed, in which the cleavage of four C(sp3)–H bonds occurred and a total of eight new bonds were formed during the synthesis of substituted dihydropyridinones in the presence of peroxide. Furthermore, dihydropyridinones have been transformed into pyridinones using KOtBu in DMSO.

Graphical abstract: KOtBu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones

Supplementary files

Article information

Article type
Communication
Submitted
09 Apr 2015
Accepted
04 Jun 2015
First published
04 Jun 2015
This article is Open Access
Creative Commons BY license

Chem. Commun., 2015,51, 11658-11661

KOtBu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones

A. Yadav, A. Verma, S. Patel, A. Kumar, V. Rathore, Meenakshi, S. Kumar and S. Kumar, Chem. Commun., 2015, 51, 11658 DOI: 10.1039/C5CC02964C

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