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Structure-Activity Relationship of Diacylhydrazine Derivatives Fluoride-Containing Pyrazolyl Moiety
Corresponding Author(s) : Hui-Min Bi
Asian Journal of Chemistry,
Vol. 25 No. 15 (2013): Vol 25 Issue 15
Abstract
Diacylhydrazine derivatives fluoride-containing pyrazolyl moiety compounds were studied by Gaussian03. They have good herbicidal activity. The optimized geometries were calculated and the information of their electron density of these compounds and energy levels, main composition and proportion of the frontier orbitals were obtained by the HF method. The structure-activity relationship was discussed and the possible mechanism was suggested. It could provide guidance for configuration of these compounds to improve the biological activity.
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- X.Y. Zhang, Y.S. Li, J.Q. Weng and C.X. Tan, Chin. J. Org. Chem., 31,1295 (2011)
- S.L. Labhade and V.B. Gaikwad, Asian J. Chem., 21, 7117 (2009).
- J.J. Heller, H. Mattioda, E. Klein and A. Sagenmuller, Brighton Crop Protection Conference Pests and Diseases, Brighton, 1, 59 (2000).
- X.H. Liu, Y.X. Shi, Y. Ma, C.Y. Zhang, W.L. Dong, P. Li, B.L. Wang, B.J. Li and Z.M. Li, Eur. J. Med. Chem., 44, 2782 (2009).
- X.H. Liu, Y.X. Shi, Y. Ma, G.R. He, W.L. Dong, C.Y. Zhang, B.L. Wang, S.H. Wang, B.J. Li and Z.M. Li, Chem. Biol. Drug Des., 73, 320 (2009).
- G.C.L. Ee, S.H. Teo, R. Go, C.K. Lim, Y.M. Lim and C.F.J. Bong, Asian J. Chem., 24, 231 (2012).
- B.K. Sharma, Yashwant and B. Srivastava, Asian J. Chem., 22, 8231 (2010).
- T.B. Wei, Y.L. Leng, Y.C. Wang, J.H. Zhang and Y.M. You, Chin. J. Org. Chem., 29, 216 (2009).
- G.F. Yang, H.Y. Liu, Z.H. Yang and X.F. Yang, Acta Chim. Sin., 56, 729 (1998).
- D.B. Zhang, Y.H. Ren, D.W. Fu, B. Yan, J.R. Song and X.Q. Lv, Acta Chim. Sin., 66, 2409 (2008).
References
X.Y. Zhang, Y.S. Li, J.Q. Weng and C.X. Tan, Chin. J. Org. Chem., 31,1295 (2011)
S.L. Labhade and V.B. Gaikwad, Asian J. Chem., 21, 7117 (2009).
J.J. Heller, H. Mattioda, E. Klein and A. Sagenmuller, Brighton Crop Protection Conference Pests and Diseases, Brighton, 1, 59 (2000).
X.H. Liu, Y.X. Shi, Y. Ma, C.Y. Zhang, W.L. Dong, P. Li, B.L. Wang, B.J. Li and Z.M. Li, Eur. J. Med. Chem., 44, 2782 (2009).
X.H. Liu, Y.X. Shi, Y. Ma, G.R. He, W.L. Dong, C.Y. Zhang, B.L. Wang, S.H. Wang, B.J. Li and Z.M. Li, Chem. Biol. Drug Des., 73, 320 (2009).
G.C.L. Ee, S.H. Teo, R. Go, C.K. Lim, Y.M. Lim and C.F.J. Bong, Asian J. Chem., 24, 231 (2012).
B.K. Sharma, Yashwant and B. Srivastava, Asian J. Chem., 22, 8231 (2010).
T.B. Wei, Y.L. Leng, Y.C. Wang, J.H. Zhang and Y.M. You, Chin. J. Org. Chem., 29, 216 (2009).
G.F. Yang, H.Y. Liu, Z.H. Yang and X.F. Yang, Acta Chim. Sin., 56, 729 (1998).
D.B. Zhang, Y.H. Ren, D.W. Fu, B. Yan, J.R. Song and X.Q. Lv, Acta Chim. Sin., 66, 2409 (2008).