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.

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Publication Details

Journal
Synlett
Published
2024-10-02
DOI
https://doi.org/10.1055/s-0043-1775058
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.25
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article

A Metal-Free Strategy for the Synthesis of Symmetrical 2,3,5,6-Tetrasubstituted Pyridines Using Triethyl Orthoformate as a Carbon Source

Jian Yuan, Suqin Shang, Wanqian Ma, Suzhen Li et al.
1 citations
Synlett
Catalytic C–H Functionalization Methods
0.25
article

A Metal-Free Strategy for the Synthesis of Symmetrical 2,3,5,6-Tetrasubstituted Pyridines Using Triethyl Orthoformate as a Carbon Source

Jian Yuan, Suqin Shang, Wanqian Ma, Suzhen Li, Yibo Song, Mengyi Guo, Xiuyu Zhang, Yanwu Li, Luoteng Cheng, Yifan Song, Qian Guo
article en
1 citations

Abstract

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.

SynlettVol. 36(06)
Openalex Percentile: Top 48%
Catalytic C–H Functionalization Methods
0.25
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