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Synthesis and Insecticidal Activity of Two New Chlorantraniliprole Derivatives
Corresponding Author(s) : Dequn Sun
Asian Journal of Chemistry,
Vol. 26 No. 1 (2014): Vol 26 Issue 1
Abstract
Two chlorantraniliprole derivatives were designed and synthesized. Their structures were characterized by 1H NMR, 13C NMR and HR-MS. Biological assay showed compounds 2, 3 had 40 % activity and 60 % activity against oriented armyworm at the concentration 5 mg/L and 200 mg/L respectively.
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- R.L. Chen and Z.S. Bao, Insect Sci. Appl., 8, 571 (1987).
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- G.P. Lahm, T.P. Selbey and T.M. Stevenson, CN1003913380.
- T. Masaki, Mol. Pharmacol., 69, 1733 (2006); doi:10.1124/mol.105.020339.
- G.P. Lahm and S.F. Mccann, WO03015518A1 (2003).
- R.A. Berger and J.L. Flexner, WO03024222A1 (2003).
References
R.L. Chen and Z.S. Bao, Insect Sci. Appl., 8, 571 (1987).
J.R. Bloomquist, Annu. Rev. Entomol., 41, 163 (1996); doi:10.1146/annurev.en.41.010196.001115.
L.M. Hall, D. Ren, G. Feng, D.F. Eberl, M. Dubald, M. Yang, F. Hannan, C.T. Kousky and W. Zheng, Molecular Actions of Insecticides on Ion Channels, American Chemical Society, ed. J.M. Clark, Washington, DC, p. 162–172, (1995).
D. Cordova, E.A. Benner, M.D. Sacher, J.J. Rauh, J.S. Sopa, G.P. Lahm, T.P. Selby, T.M. Stevenson, L. Flexner, S. Gutteridge, D.F. Rhoades, L. Wu, R.M. Smith and Y. Tao, Pestic. Biochem. Physiol., 84, 196 (2006); doi:10.1016/j.pestbp.2005.07.005.
Q. Feng, Z.L. Liu, L.X. Xiong, M.-Z. Wang, Y.-Q. Li and Z.-M. Li, J. Agric. Food Chem., 58, 12327 (2010); doi:10.1021/jf102842r.
G.P. Lahm, T.M. Stevenson, T.P. Selby, J.H. Freudenberger, D. Cordova, L. Flexner, C.A. Bellin, C.M. Dubas, B.K. Smith, K.A. Hughes, J.G. Hollingshaus, C.E. Clark and E.A. Benner, Bioorg. Med. Chem. Lett., 17, 6279 (2007); doi:10.1016/j.bmcl.2007.09.012.
G.P. Lahm, T.P. Selbey and T.M. Stevenson, CN1003913380.
T. Masaki, Mol. Pharmacol., 69, 1733 (2006); doi:10.1124/mol.105.020339.
G.P. Lahm and S.F. Mccann, WO03015518A1 (2003).
R.A. Berger and J.L. Flexner, WO03024222A1 (2003).