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Synlett 2025; 36(06): 709-713
DOI: 10.1055/s-0043-1775058
DOI: 10.1055/s-0043-1775058
letter
A Metal-Free Strategy for the Synthesis of Symmetrical 2,3,5,6-Tetrasubstituted Pyridines Using Triethyl Orthoformate as a Carbon Source

Abstract
A simple and efficient method for the synthesis of symmetric 2,3,5,6-tetrasubstituted pyridines from enaminones and triethyl orthoformate, catalyzed by pyridinium p-toluenesulfonate, has been established in which triethyl orthoformate was applied as a carbon source. The procedure was smoothly executed, culminating in the synthesis of symmetrical 2,3,5,6-tetrasubstituted pyridines with moderate to exceptional yields across a diverse array of substrates.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0043-1775058.
- Supporting Information
Publication History
Received: 14 June 2024
Accepted after revision: 15 August 2024
Article published online:
02 October 2024
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