Chem. J. Chinese Universities ›› 2009, Vol. 30 ›› Issue (5): 908.

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Synthesis and Biological Activities of 3-Substituent-5-aryloxazolidin-4-ones

YAO Hong-Wei, LI Huan-Huan, SU Na-Na, WANG Hong-Xue, LIU Xing-Hai, WANG Li-Zhong, ZHANG Xiao, LI Zheng-Ming, ZHAO Wei-Guang*   

  1. State Key Laboratory of Elemento-organic Chemistry, National Pesticide Engineering Research Center, Nankai University, Tianjin 300071, China
  • Received:2008-11-05 Online:2009-05-10 Published:2009-05-10
  • Contact: ZHAO Wei-Guang, E-mail: zwg@nankai.edu.cn

Abstract:

Mandipropamid is the first mandelamide fungicide on the market. Cyclizing open structures in a given structure represents one of the useful methods in the search for biologically active conformations. A series of novel 3-substituentphenethyl-5-aryloxazolidin-4-ones, the ring-closed analogues of mandipropamid, were obtained from the 2-hydroxy-N-(substitutedphenethyl)-2-arylacetamide and aldehydes by refluxing in benzene or toluene with catalytic amount of p-toluenesulphonic acid. Their structures were identified by means of elemental analysis, IR, 1H NMR and MS spectra. And their structure-activity relationships were discussed.

Key words: Oxazolidinone, Mandelamide, Biological activity

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