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Synthesis and Activity of Novel Fungicide 2-(3-Chlorophenylcarbamoyl)phenyl Acetate
Corresponding Author(s) : Shirong Jiao
Asian Journal of Chemistry,
Vol. 27 No. 7 (2015): Vol 27 Issue 7, 2015
Abstract
In the present study, 2-(3-chlorophenylcarbamoyl)phenyl acetate was synthesized by the ammonolysis of 2-(chlorocarbonyl)phenyl acetate. Its structure was confirmed by IR and 1H NMR. Its antifungal activity against Sclerotinia sclerotiorum and Helminthosprium maydis has been determined in the laboratory. The results showed that it had good antifungal activity against the two different pathogenic fungi of plants. Its median effective concentrations (EC50) reached 2 and 3.80 mg L-1, respectively.
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- X.J. Chen, M.J. Cao, Y. Wang, Y.H. Tong and J.Y. Xu, Chin. J. Oil Crop Sci., 31, 503 (2009).
- Y.L. Pan, Z.Y. Wang and H.Z. Wu, J. Jiangsu Agric., 13, 32 (1997).
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- D.G. Hutton, Australas. Plant Pathol., 17, 34 (1988); doi:10.1071/APP9880034.
- Y.X. Qi, F.X. Chen and K.J. Ding, Pesticides, 8, 567 (2006).
- FAO Plant Prot. Bull., 30, 30 (1982).
- A. ten Have, R. van Berloo, P. Lindhout and J.A.L. van Kan, Eur. J. Plant Pathol., 113, 153 (2007); doi:10.1007/s10658-006-9081-9.
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References
X.J. Chen, M.J. Cao, Y. Wang, Y.H. Tong and J.Y. Xu, Chin. J. Oil Crop Sci., 31, 503 (2009).
Y.L. Pan, Z.Y. Wang and H.Z. Wu, J. Jiangsu Agric., 13, 32 (1997).
Z.Q. Shi, M.G. Zhou and Z.Y. Ye, J. Jiangsu Agric., 16, 212 (2000).
W. Li, Y.J. Zhou and H.G. Chen, Chin. J. Oil Crop Sci., 29, 63 (2007).
K.Y. Liu and F.X. Chen, Anhui Agric. Sci., 35, 756 (2007).
D.G. Hutton, Australas. Plant Pathol., 17, 34 (1988); doi:10.1071/APP9880034.
Y.X. Qi, F.X. Chen and K.J. Ding, Pesticides, 8, 567 (2006).
FAO Plant Prot. Bull., 30, 30 (1982).
A. ten Have, R. van Berloo, P. Lindhout and J.A.L. van Kan, Eur. J. Plant Pathol., 113, 153 (2007); doi:10.1007/s10658-006-9081-9.
S.I. Ignatova, N.S. Gorshkova and T.A. Tereshonkova, Acta Physiol. Plant., 22, 326 (2000); doi:10.1007/s11738-000-0047-9.
H. Egashira, A. Kuwashima, H. Ishiguro, K. Fukushima, T. Kaya and S. Imanishi, Acta Physiol. Plant., 22, 324 (2000); doi:10.1007/s11738-000-0046-x.
R.L. Guimaraes, R.T. Chetelat and H.U. Stotz, Eur. J. Plant Pathol., 110, 13 (2004); doi:10.1023/B:EJPP.0000010133.62052.e4.
R. Finkers, P. Berg, R. Berloo, A. Have, A.W. Heusden, J.A.L. Kan and P. Lindhout, Theor. Appl. Genet., 114, 585 (2007); doi:10.1007/s00122-006-0458-0.
X. Wang, Med. Hypotheses, 50, 239 (1998); doi:10.1016/S0306-9877(98)90024-X.
D.W. Gilroy, Prostag. Leukotr. Ess., 73, 203 (2005); doi:10.1016/j.plefa.2005.05.007.
C. Millikan and N. Futrell, J. Stroke Cerebrovasc. Dis., 5, 248 (1995); doi:10.1016/S1052-3057(10)80199-5.
J.R. Vane, R.J. Flower and R.M. Botting, Stroke, 21(Suppl.), IV12 (1990).
M.L. Dyken, H.J.M. Barnett, J.D. Easton, W.S. Fields, V. Fuster, V. Hachinski, J.W. Norris and D.G. Sherman, Stroke, 23, 1395 (1992); doi:10.1161/01.STR.23.10.1395.
H. Tohgi, S. Konno, K. Tamura, B. Kimura and K. Kawano, Stroke, 23, 1400 (1992); doi:10.1161/01.STR.23.10.1400.
R.H. Ackerman and K.L. Newman, Ann. Neurol., 28, 224 (1990).
C.M. Helgason, K.L. Tortorice, S.R. Winkler, D.W. Penney, J.J. Schuler, T.J. McClelland and L.D. Brace, Stroke, 24, 345 (1993); doi:10.1161/01.STR.24.3.345.
W.K. Hass, J.D. Easton, H.P. Adams Jr., W. Pryse-Phillips, B.A. Molony, S. Anderson and B. Kamm, N. Engl. J. Med., 321, 501 (1989); doi:10.1056/NEJM198908243210804.
D.M. McCarthy, Best Pract. Res. Cl. Ga., 26, 101 (2012); doi:10.1016/j.bpg.2012.01.008.
W. Huang and G.F. Yang, Bioorg. Med. Chem., 14, 8280 (2006); doi:10.1016/j.bmc.2006.09.016.