Copyright (c) 2014 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Phase Transfer Catalyzed Synthesis and Biological Activity of Thiourea Derivatives Containing 1,2,3-Thiadiazole Moiety
Corresponding Author(s) : Xing-Hai Liu
Asian Journal of Chemistry,
Vol. 26 No. 21 (2014): Vol 26 Issue 21
Abstract
A series of N-(substituted-phenyl)-N'-(4-methyl-1,2,3-thiadiazole-5-yl)-thiourea (7a-7e) were
synthesized and characterized. The chemical structures of all the compounds were confirmed
by 1H NMR, MS and elemental analysis. All the compounds were investigated for fungicidal
activity and plant growth regulatory activity. The bioassay results indicated that some of these
compound exhibit moderate fungicidal activities.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- S. Nanjunda Swamy, Basappa, G. Sarala, B.S. Priya, S.L. Gaonkar, J. Shashidhara Prasad and K.S. Rangappa, Bioorg. Med. Chem. Lett., 16, 999 (2006); doi:10.1016/j.bmcl.2005.10.084.
- F.Q. He, X.H. Liu, B.L. Wang and Z.M. Li, Heteroatom Chem., 19, 21 (2008); doi:10.1002/hc.20369.
- X.D. Yang, Heterocycl. Commun., 13, 387 (2007); doi:10.1515/HC.2007.13.6.387.
- S. Yang, Z. Li, L. Jin, B. Song, G. Liu, J. Chen, Z. Chen, D. Hu, W. Xue and R. Xu, Bioorg. Med. Chem. Lett., 17, 2193 (2007); doi:10.1016/j.bmcl.2007.01.101.
- K. Tsubata, O. Sanpei, K. Takagi, K. Umetani, T. Uchikurohane and S. Tajima, WO 9923084 (1999); Chem. Abstr., 130, 311799 (1999).
- W. Kunz, R. Schurter and T. Maetzke, Pestic. Sci., 50, 275 (1997); doi:10.1002/(SICI)1096-9063(199708)50:4<275::AID-PS593>3.0.CO;2-7.
- C.B. Ziegler Jr., W.V. Curran, N.A. Kuck, S.M. Harris and Y. Lin, J. Heterocycl. Chem., 26, 1141 (1989); doi:10.1002/jhet.5570260444.
- X.Q. He, W.M. Tang, B.A. Song, D.Y. Hu, L.L. Pang, W.J. Sang, S. Yang and L.H. Jin, Chin. J. Org. Chem., 24, 1284 (2004).
- S.A.F. Rostom, Bioorg. Med. Chem., 14, 6475 (2006); doi:10.1016/j.bmc.2006.06.020.
- A. Lukomska and J. Sobkowski, J. Electroanal. Chem., 592, 68 (2006); doi:10.1016/j.jelechem.2006.04.010.
- G. Binzet, H. Arslan, U. Flörke, N. Külcü and N. Duran, J. Coord. Chem., 59, 1395 (2006); doi:10.1080/00958970500512633.
- Y.H. Dong and Z.X. Si, Chin. J. Appl. Chem., 12, 62 (1995).
- P. Sharma, A. Kumar and P. Pandey, Indian J. Chem., 45B, 2077 (2006).
- T.B. Wei, H. Wang, Q. Lin and Y.M. Zhang, Chin. J. Org. Chem., 25, 1565 (2005).
References
S. Nanjunda Swamy, Basappa, G. Sarala, B.S. Priya, S.L. Gaonkar, J. Shashidhara Prasad and K.S. Rangappa, Bioorg. Med. Chem. Lett., 16, 999 (2006); doi:10.1016/j.bmcl.2005.10.084.
F.Q. He, X.H. Liu, B.L. Wang and Z.M. Li, Heteroatom Chem., 19, 21 (2008); doi:10.1002/hc.20369.
X.D. Yang, Heterocycl. Commun., 13, 387 (2007); doi:10.1515/HC.2007.13.6.387.
S. Yang, Z. Li, L. Jin, B. Song, G. Liu, J. Chen, Z. Chen, D. Hu, W. Xue and R. Xu, Bioorg. Med. Chem. Lett., 17, 2193 (2007); doi:10.1016/j.bmcl.2007.01.101.
K. Tsubata, O. Sanpei, K. Takagi, K. Umetani, T. Uchikurohane and S. Tajima, WO 9923084 (1999); Chem. Abstr., 130, 311799 (1999).
W. Kunz, R. Schurter and T. Maetzke, Pestic. Sci., 50, 275 (1997); doi:10.1002/(SICI)1096-9063(199708)50:4<275::AID-PS593>3.0.CO;2-7.
C.B. Ziegler Jr., W.V. Curran, N.A. Kuck, S.M. Harris and Y. Lin, J. Heterocycl. Chem., 26, 1141 (1989); doi:10.1002/jhet.5570260444.
X.Q. He, W.M. Tang, B.A. Song, D.Y. Hu, L.L. Pang, W.J. Sang, S. Yang and L.H. Jin, Chin. J. Org. Chem., 24, 1284 (2004).
S.A.F. Rostom, Bioorg. Med. Chem., 14, 6475 (2006); doi:10.1016/j.bmc.2006.06.020.
A. Lukomska and J. Sobkowski, J. Electroanal. Chem., 592, 68 (2006); doi:10.1016/j.jelechem.2006.04.010.
G. Binzet, H. Arslan, U. Flörke, N. Külcü and N. Duran, J. Coord. Chem., 59, 1395 (2006); doi:10.1080/00958970500512633.
Y.H. Dong and Z.X. Si, Chin. J. Appl. Chem., 12, 62 (1995).
P. Sharma, A. Kumar and P. Pandey, Indian J. Chem., 45B, 2077 (2006).
T.B. Wei, H. Wang, Q. Lin and Y.M. Zhang, Chin. J. Org. Chem., 25, 1565 (2005).