Issue 4, 2017

Synthesis of tetrasubstituted symmetrical pyridines by iron-catalyzed cyclization of ketoxime acetates

Abstract

An efficient iron-catalyzed cyclization of ketoxime acetates with N,N-dimethylaniline for the synthesis of symmetrical pyridines has been developed. A methyl carbon on N,N-dimethylaniline acts as a source of one carbon synthons. The reaction used readily available starting materials, tolerated various functional groups, and afforded 2,3,5,6-tetrasubstituted symmetrical pyridines in good yields.

Graphical abstract: Synthesis of tetrasubstituted symmetrical pyridines by iron-catalyzed cyclization of ketoxime acetates

Supplementary files

Article information

Article type
Research Article
Submitted
13 Dec 2016
Accepted
22 Jan 2017
First published
23 Jan 2017

Org. Chem. Front., 2017,4, 597-602

Synthesis of tetrasubstituted symmetrical pyridines by iron-catalyzed cyclization of ketoxime acetates

M. Zhao, L. Yu, N. Mo, Z. Ren, Y. Wang and Z. Guan, Org. Chem. Front., 2017, 4, 597 DOI: 10.1039/C6QO00809G

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