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Synthesis and Characterization of Salamo-Type Bisoxime Compounds Based on 2-Hydroxy-4-methoxybenzaldehyde and Bis(aminooxy)alkane
Corresponding Author(s) : Li Wang
Asian Journal of Chemistry,
Vol. 26 No. 18 (2014): Vol 26 Issue 18
Abstract
Three new Salamo-type bisoxime compounds H2L1-H2L3 have been synthesized from 2-hydroxy-4-methoxybenzaldehyde and 1,5-bis(aminooxy)pentane, 1,6-bis(aminooxy)hexane or 1,9-bis(aminooxy)nonane in hot ethanol medium, respectively and characterized by elemental analysis, IR and 1H NMR spectroscopy.
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- H.L. Wang, D.P. Zhang, Z.H. Ni, X.Y. Li, L.J. Tian and J.Z. Jiang, Inorg. Chem., 48, 5946 (2009); doi:10.1021/ic9002862.
- J.K. Karjalainen, O.E.O. Hormi and D.C. Sherrington, Tetrahedron Asymm., 9, 3895 (1998); doi:10.1016/S0957-4166(98)00408-X.
- H. Chen and J. Rhodes, J. Mol. Med., 74, 497 (1996); doi:10.1007/BF00204975.
- A. Iqbal, H.L. Siddiqui, CM. Ashraf, M.H. Bukhari and C.M. Akram, Chem. Pharm. Bull. (Tokyo), 55, 1070 (2007); doi:10.1248/cpb.55.1070.
- S.T. Girousi, E.E. Golia, A.N. Voulgaropoulos and A.J. Maroulis, Fresenius J. Anal. Chem., 358, 667 (1997); doi:10.1007/s002160050488.
- M.N. Desal, P.O. Chauhan and N. Shan, Europ. Symp. Corrision Inhibitors, 27, 891 (1995).
- S. Akine, T. Tadokoro and T. Nabeshima, Inorg. Chem., 51, 11478 (2012); doi:10.1021/ic3012525.
- W.K. Dong, X.N. He, H.B. Yan, Z.W. Lv, X. Chen, C.Y. Zhao and X.L. Tang, Polyhedron, 28, 1419 (2009); doi:10.1016/j.poly.2009.03.017.
- W.K. Dong, C.Y. Zhao, Y.X. Sun, X.L. Tang and X.N. He, Inorg. Chem. Commun., 12, 234 (2009); doi:10.1016/j.inoche.2008.12.019.
- S. Akine, T. Taniguchi, W. Dong, S. Masubuchi and T. Nabeshima, J. Org. Chem., 70, 1704 (2005); doi:10.1021/jo048030y.
- J.A. Faniran, K.S. Patel and J.C. Bailar Jr., J. Inorg. Nucl. Chem., 36, 1547 (1974); doi:10.1016/0022-1902(74)80621-4.
- S. Akine, T. Taniguchi and T. Nabeshima, Chem. Lett., 30, 682 (2001); doi:10.1246/cl.2001.682.
References
H.L. Wang, D.P. Zhang, Z.H. Ni, X.Y. Li, L.J. Tian and J.Z. Jiang, Inorg. Chem., 48, 5946 (2009); doi:10.1021/ic9002862.
J.K. Karjalainen, O.E.O. Hormi and D.C. Sherrington, Tetrahedron Asymm., 9, 3895 (1998); doi:10.1016/S0957-4166(98)00408-X.
H. Chen and J. Rhodes, J. Mol. Med., 74, 497 (1996); doi:10.1007/BF00204975.
A. Iqbal, H.L. Siddiqui, CM. Ashraf, M.H. Bukhari and C.M. Akram, Chem. Pharm. Bull. (Tokyo), 55, 1070 (2007); doi:10.1248/cpb.55.1070.
S.T. Girousi, E.E. Golia, A.N. Voulgaropoulos and A.J. Maroulis, Fresenius J. Anal. Chem., 358, 667 (1997); doi:10.1007/s002160050488.
M.N. Desal, P.O. Chauhan and N. Shan, Europ. Symp. Corrision Inhibitors, 27, 891 (1995).
S. Akine, T. Tadokoro and T. Nabeshima, Inorg. Chem., 51, 11478 (2012); doi:10.1021/ic3012525.
W.K. Dong, X.N. He, H.B. Yan, Z.W. Lv, X. Chen, C.Y. Zhao and X.L. Tang, Polyhedron, 28, 1419 (2009); doi:10.1016/j.poly.2009.03.017.
W.K. Dong, C.Y. Zhao, Y.X. Sun, X.L. Tang and X.N. He, Inorg. Chem. Commun., 12, 234 (2009); doi:10.1016/j.inoche.2008.12.019.
S. Akine, T. Taniguchi, W. Dong, S. Masubuchi and T. Nabeshima, J. Org. Chem., 70, 1704 (2005); doi:10.1021/jo048030y.
J.A. Faniran, K.S. Patel and J.C. Bailar Jr., J. Inorg. Nucl. Chem., 36, 1547 (1974); doi:10.1016/0022-1902(74)80621-4.
S. Akine, T. Taniguchi and T. Nabeshima, Chem. Lett., 30, 682 (2001); doi:10.1246/cl.2001.682.