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.
Authors
- Jian Yuan (ORCID: https://orcid.org/0000-0002-2453-9057)
- Suqin Shang (ORCID: https://orcid.org/0000-0001-9376-0735)
- Wanqian Ma
- Suzhen Li
- Yibo Song
- Mengyi Guo
- Xiuyu Zhang (ORCID: https://orcid.org/0000-0003-4848-9004)
- Yanwu Li (ORCID: https://orcid.org/0000-0002-8794-659X)
- Luoteng Cheng
- Yifan Song (ORCID: https://orcid.org/0000-0003-0565-6271)
- Qian Guo (ORCID: https://orcid.org/0000-0003-3023-2462)
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