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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...

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Detalles Bibliográficos
Autores principales: Huang, Liang-Zhu, Han, Pan, Li, You-Qiang, Xu, Ying-Meng, Zhang, Tao, Du, Zhen-Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
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
Descripción
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.