Chem. J. Chinese Universities ›› 1998, Vol. 19 ›› Issue (12): 1970.

• Articles • Previous Articles     Next Articles

The Synthesis and Biological Activity of Diethyl N-(2-Benzothiazolyl)-α-aminoalkylphosphonate

LI Zai-Guo, HUANG Run-Qiu, YANG Zhao, LI Hui-Ying   

  1. Institute and State Key Laboratory of Elemento organic Chemistry, Nankai University, Tianjin, 300071
  • Received:1997-12-16 Online:1998-12-24 Published:1998-12-24

Abstract: Twenty diethyl N-(2-benzothiazolyl)-α-aminoalkylphosphonates were synthesized by addition of diethyl phosphite to the corresponding imine. The reaction phenomenon was explained by a concerted 3+2 mechanism. The atomic charge of imine was calculated by quantum chemistry(MINDO/3) and the effect of substitutes on the formation of pentacyclic transition state was discussed. Some compounds showed a very good inhibitory effect against tobacco mosaic virus(TMV) and herbicidal activity.

Key words: 2-Aminobenzothiazole, α-Aminoalkylphosphonate, Concerted 3+2 mechanism, Atomic charge, Tobacco mosaic virus

CLC Number: 

TrendMD: