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A Facile and Efficient Synthesis of Diaryl Amines or Ethers under Microwave Irradiation at Presence of KF/Al(2)O(3) without Solvent and Their Anti-Fungal Biological Activities against Six Phytopathogens
A series of diaryl amines, ethers and thioethers were synthesized under microwave irradiation efficiently at presence of KF/Al(2)O(3) in 83%–96% yields without any solvent. The salient characters of this method lie in short reaction time, high yields, general applicability to substrates and simple w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794810/ https://www.ncbi.nlm.nih.gov/pubmed/24036444 http://dx.doi.org/10.3390/ijms140918850 |
Sumario: | A series of diaryl amines, ethers and thioethers were synthesized under microwave irradiation efficiently at presence of KF/Al(2)O(3) in 83%–96% yields without any solvent. The salient characters of this method lie in short reaction time, high yields, general applicability to substrates and simple workup procedure. At the same time, their antifungal biological activities against six phytopathogen were evaluated. Most of the compounds (3b, 3c, 3g–o) are more potent than thiophannate-methyl against to Magnaporthe oryzae. This implies that diaryl amine or ether moiety may be helpful in finding a fungicide against Magnaporthe oryzae. |
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