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Synthesis, Characterization and Pesticide Activities of Some Novel Tutin Derivatives
Corresponding Author(s) : Menglou Li
Asian Journal of Chemistry,
Vol. 25 No. 10 (2013): Vol 25 Issue 10
Abstract
Seven novel tutin acylation derivatives (T1-T7) were synthesized to determine their pesticide activity against Mythimna separata. The structural assignments of these semisynthetic compounds were examined based on their IR, ESIMS and 1H- and 13C-NMR spectra data. Compared with tutin, those derivatives possessing potent anti-feedant activity and the most potent was 2-(3,5-dichlorobenzoyloxy)-tutin (T7).
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- J. Fuentealba, B. Munoz, G. Yevenes, G. Moraga-Cid, C. Pérez, L. Guzman, J.M. Rigo and L.G. Aguayo, Neuropharmacology, 60, 453 (2011).
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- C. Ioriatti, E. Pasqualini, D. Pasquier and C. Tomasi, J. Pest. Sci., 79, 163 (2006).
- M.S. Godoy, G.A. Carvalho, J.C. Moraes, M.G. Junior, A.A. Moraise and L.V. Cosme, Neotrop. Entomol., 33, 639 (2004).
References
J. Fuentealba, B. Munoz, G. Yevenes, G. Moraga-Cid, C. Pérez, L. Guzman, J.M. Rigo and L.G. Aguayo, Neuropharmacology, 60, 453 (2011).
H. Zhou, Y.H. Tang and Y. Zheng, Brain Res., 1092, 207 (2006).
L.J. Zhou, L.C. Song, R.T. Ruo, Z.R. Yang and C. He, J. Sichuan Uni. (Nat. Sci. Ed.), 43, 1165 (2006).
M.L. Li, J. Cui, R.H. Qin, J.M. Gao, Y.B. Zhang, X.R. Guo and W. Zhang, Heterocycles, 71, 1155 (2007).
Y. Kudo, H. Niwa, A. Tanaka and K. Yamada, Br. J. Pharmacol., 81, 373 (1984).
C. Ioriatti, E. Pasqualini, D. Pasquier and C. Tomasi, J. Pest. Sci., 79, 163 (2006).
M.S. Godoy, G.A. Carvalho, J.C. Moraes, M.G. Junior, A.A. Moraise and L.V. Cosme, Neotrop. Entomol., 33, 639 (2004).