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Synthesis of Arylfurfural Oximes and Their Biological Evaluation
Corresponding Author(s) : Samina Aslam
Asian Journal of Chemistry,
Vol. 28 No. 6 (2016): Vol 28 Issue 6
Abstract
Various oximes of arylfurfural were prepared and characterized through elemental analysis and spectroscopic techniques (FTIR, 1H NMR, 13C NMR and Mass). Synthesized compounds were tested for their antioxidant, tyrosinase and chemotrypson activities.
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- S.R. Sandier and W. Karo, Organic Functional Group Preparations, Academic Press: San Diego, edn 2, pp 431-476 (1989).
- T.W. Greene and P.G.M. Wuts, Protective Groups in Organic Synthesis, Wiley: Toronto, edn 3, pp 355-358 (1999).
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- P.A.S. Smith and S.E. Gloyer, J. Org. Chem., 40, 2508 (1975); doi:10.1021/jo00905a019.
- S. Negi, M. Matsukura, M. Mizuno, K. Miyake and N. Minami, Synthesis, 991 (1996); doi:10.1055/s-1996-4325.
- K. Narasaka, Pure Appl. Chem., 75, 19 (2003); doi:10.1351/pac200375010019.
- J.K. Whitesell and M.A. Whitesell, Synthesis, 517 (1983); doi:10.1055/s-1983-30409.
- C. Ramalingan and Y.-T. Park, J. Org. Chem., 72, 4536 (2007); doi:10.1021/jo070297k.
- Y. Furuya, K. Ishihara and H. Yamamoto, J. Am. Chem. Soc., 127, 11240 (2005); doi:10.1021/ja053441x.
- B.A. Song, X.H. Liu, S. Yang, D.Y. Hu, L.H. Jin and Y.T. Zhang, Chin. J. Org. Chem., 25, 507 (2005).
- H. Hamaguchi, O. Kajihara and M. Katoh, J. Pestic. Sci., 20, 173 (1995); doi:10.1584/jpestics.20.173.
- T.J. Venanzi and C.A. Venanzi, J. Comput. Chem., 9, 67 (1988); doi:10.1002/jcc.540090109.
- H. Dai, H.-B. Yu, J.-B. Liu, Y.-Q. Li, X. Qin, X. Zhang, Z.-F. Qin, T.-T. Wang and J.-X. Fang, ARKIVOC, 126 (2009); doi:10.3998/ark.5550190.0010.713.
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- D. Metodiewa, A. Kochman and S. Karolczak, Biochem. Mol. Biol. Int., 41, 1067 (1997).
- M.A. Khan and J.B. Polya, Aust. J. Chem., 26, 1147 (1973); doi:10.1071/CH9731147.
- M.A. Khan and S.M.L. Uberti, Rev. Latinoamer. Quim., 14, 79 (1983).
- M. Athar, M.A. Khan and S.M.L. Uberti, J. Pure Appl. Sci., 22, 129 (2003).
- S. Aslam, N. Asif, M.N. Khan, M.A. Khan, M.A. Munawar and M. Nasrullah, Asian J. Chem., 25, 7738 (2013); doi:10.14233/ajchem.2013.14590A.
References
S.R. Sandier and W. Karo, Organic Functional Group Preparations, Academic Press: San Diego, edn 2, pp 431-476 (1989).
T.W. Greene and P.G.M. Wuts, Protective Groups in Organic Synthesis, Wiley: Toronto, edn 3, pp 355-358 (1999).
S.K. Dewan, R. Singh and A. Kumar, ARKIVOC, 41 (2006); doi:10.3998/ark.5550190.0007.204.
P.R. Dave, F. Forohar, T. Axenrod, K.K. Das, L. Qi, C. Watnick and H. Yazdekhasti, J. Org. Chem., 61, 8897 (1996); doi:10.1021/jo9614755.
F.P. Ballistreni, E. Barbuzzi, G.A. Tomaselli and R.M. Toscano, Synlett., 11, 1093 (1996)’ doi:10.1055/s-1996-5666.
P.A.S. Smith and S.E. Gloyer, J. Org. Chem., 40, 2508 (1975); doi:10.1021/jo00905a019.
S. Negi, M. Matsukura, M. Mizuno, K. Miyake and N. Minami, Synthesis, 991 (1996); doi:10.1055/s-1996-4325.
K. Narasaka, Pure Appl. Chem., 75, 19 (2003); doi:10.1351/pac200375010019.
J.K. Whitesell and M.A. Whitesell, Synthesis, 517 (1983); doi:10.1055/s-1983-30409.
C. Ramalingan and Y.-T. Park, J. Org. Chem., 72, 4536 (2007); doi:10.1021/jo070297k.
Y. Furuya, K. Ishihara and H. Yamamoto, J. Am. Chem. Soc., 127, 11240 (2005); doi:10.1021/ja053441x.
B.A. Song, X.H. Liu, S. Yang, D.Y. Hu, L.H. Jin and Y.T. Zhang, Chin. J. Org. Chem., 25, 507 (2005).
H. Hamaguchi, O. Kajihara and M. Katoh, J. Pestic. Sci., 20, 173 (1995); doi:10.1584/jpestics.20.173.
T.J. Venanzi and C.A. Venanzi, J. Comput. Chem., 9, 67 (1988); doi:10.1002/jcc.540090109.
H. Dai, H.-B. Yu, J.-B. Liu, Y.-Q. Li, X. Qin, X. Zhang, Z.-F. Qin, T.-T. Wang and J.-X. Fang, ARKIVOC, 126 (2009); doi:10.3998/ark.5550190.0010.713.
G. Ouyang, Z. Chen, X.-J. Cai, B.-A. Song, P.S. Bhadury, S. Yang, L.-H. Jin, W. Xue, D.E.-Y. Hu and S. Zeng, Bioorg. Med. Chem., 16, 9699 (2008); doi:10.1016/j.bmc.2008.09.070.
D. Metodiewa, A. Kochman and S. Karolczak, Biochem. Mol. Biol. Int., 41, 1067 (1997).
M.A. Khan and J.B. Polya, Aust. J. Chem., 26, 1147 (1973); doi:10.1071/CH9731147.
M.A. Khan and S.M.L. Uberti, Rev. Latinoamer. Quim., 14, 79 (1983).
M. Athar, M.A. Khan and S.M.L. Uberti, J. Pure Appl. Sci., 22, 129 (2003).
S. Aslam, N. Asif, M.N. Khan, M.A. Khan, M.A. Munawar and M. Nasrullah, Asian J. Chem., 25, 7738 (2013); doi:10.14233/ajchem.2013.14590A.