A facile electrochemical method for the synthesis of new sulfonamide derivatives of potential biological significance
English
A facile electrochemical method for the synthesis of new sulfonamide derivatives of potential biological significance
-
-
-
[1] Z. Huang, Z. Lin, J. Huang, A novel kind of antitumour drugs using sulfonamide as parent compound, Eur. J. Med. Chem. 36 (2001) 863-872.[1] Z. Huang, Z. Lin, J. Huang, A novel kind of antitumour drugs using sulfonamide as parent compound, Eur. J. Med. Chem. 36 (2001) 863-872.
-
[2] S.F. Yang, C.F. Lin, C.J. Wu, K.K. Ng, A.Y.C. Lin, P.K.A. Hong, Fate of sulfonamide antibiotics in contact with activated sludge—sorption and biodegradation, Water Res. 46 (2012) 1301-1308.[2] S.F. Yang, C.F. Lin, C.J. Wu, K.K. Ng, A.Y.C. Lin, P.K.A. Hong, Fate of sulfonamide antibiotics in contact with activated sludge—sorption and biodegradation, Water Res. 46 (2012) 1301-1308.
-
[3] K. Seri, K. Sanai, K. Kurashima, Y. Imamura, H. Akita, (R)-ACX is a novel sufonylurea compound with potent, quick and short-lasting hypoglycemic activity, Eur. J. Pharmacol. 389 (2000) 253-256.[3] K. Seri, K. Sanai, K. Kurashima, Y. Imamura, H. Akita, (R)-ACX is a novel sufonylurea compound with potent, quick and short-lasting hypoglycemic activity, Eur. J. Pharmacol. 389 (2000) 253-256.
-
[4] S. Bano, J. Javed, S. Ahmad, I.G. Rathish, S. Singh, M.S. Alam, Synthesis and biological evaluation of some new 2-pyrazolines bearing benzene sulfonamide moiety as potential anti-inflammatory and anti-cancer agents, Eur. J. Med. Chem. 46 (2011) 5763-5768.[4] S. Bano, J. Javed, S. Ahmad, I.G. Rathish, S. Singh, M.S. Alam, Synthesis and biological evaluation of some new 2-pyrazolines bearing benzene sulfonamide moiety as potential anti-inflammatory and anti-cancer agents, Eur. J. Med. Chem. 46 (2011) 5763-5768.
-
[5] X.P. Hong, J.Y. Ma, Electrochemical study of sulfadiazine on a novel phthalocyanine- containing chemically modified electrode, Chin. Chem. Lett. 24 (2013) 329- 331.[5] X.P. Hong, J.Y. Ma, Electrochemical study of sulfadiazine on a novel phthalocyanine- containing chemically modified electrode, Chin. Chem. Lett. 24 (2013) 329- 331.
-
[6] R. Sivakumar, S.K. Gnanasam, S. Ramachandran, Pharmacological evaluation of some new 1-substituted-4-hydroxy-phthalazines, Eur. J. Med. Chem. 37 (2002) 79-8013.[6] R. Sivakumar, S.K. Gnanasam, S. Ramachandran, Pharmacological evaluation of some new 1-substituted-4-hydroxy-phthalazines, Eur. J. Med. Chem. 37 (2002) 79-8013.
-
[7] S.L. Zhang, Y.J. Liu, Y.F. Zhao, Q.T. Guo, P. Gong, Synthesis and antitumor activities of novel 1,4-substituted phthalazine derivatives, Chin. Chem. Lett. 21 (2010) 1071-1074.[7] S.L. Zhang, Y.J. Liu, Y.F. Zhao, Q.T. Guo, P. Gong, Synthesis and antitumor activities of novel 1,4-substituted phthalazine derivatives, Chin. Chem. Lett. 21 (2010) 1071-1074.
-
[8] X. Zhai, J. Li, L. He, S. Zheng, Y.B. Zhang, P. Gong, Synthesis and in vitro cytotoxicity of novel 1,4-disubstituted phthalazines, Chin. Chem. Lett. 19 (2008) 29-32.[8] X. Zhai, J. Li, L. He, S. Zheng, Y.B. Zhang, P. Gong, Synthesis and in vitro cytotoxicity of novel 1,4-disubstituted phthalazines, Chin. Chem. Lett. 19 (2008) 29-32.
-
[9] D. Nematollahi, A. Maleki, Electrochemical oxidaton of N,N-dialkyl-π-πhenylenediaminesin the presence of arylsulfinic acids. An efficient method for the synthesisof new sulfonamide derivatives, Electrochem. Commun. 11 (2009) 488-491.[9] D. Nematollahi, A. Maleki, Electrochemical oxidaton of N,N-dialkyl-π-πhenylenediaminesin the presence of arylsulfinic acids. An efficient method for the synthesisof new sulfonamide derivatives, Electrochem. Commun. 11 (2009) 488-491.
-
[10] D. Nematollahi, E. Mehdipour, A. Zeinodini-Meimand, A. Maleki, Chemical and electrochemical oxidative coupling of N,N-dialkyl-π-πhenylenediamines and arylsulfinic acids. Synthesis of sulfonamide derivatives, Tetrahedron Lett. 51 (2010) 6447-6450.[10] D. Nematollahi, E. Mehdipour, A. Zeinodini-Meimand, A. Maleki, Chemical and electrochemical oxidative coupling of N,N-dialkyl-π-πhenylenediamines and arylsulfinic acids. Synthesis of sulfonamide derivatives, Tetrahedron Lett. 51 (2010) 6447-6450.
-
[11] F. Varmaghani, D. Nematollahi, S.E. Mallakpour, R. Esmaili, Electrochemical oxidation of 4-substituted urazoles in the presence of arylsulfinic acids: an efficient method for the synthesis of new sulfonamide derivatives, Green Chem. 14 (2012) 963-967.[11] F. Varmaghani, D. Nematollahi, S.E. Mallakpour, R. Esmaili, Electrochemical oxidation of 4-substituted urazoles in the presence of arylsulfinic acids: an efficient method for the synthesis of new sulfonamide derivatives, Green Chem. 14 (2012) 963-967.
-
[12] F. Varmaghani, D. Nematollahi, Electrochemical study of 1,2-dihydropyridazine- 3,6-dione in protic and aprotic solvents: oxidative ring cleavage and reduction, Electrochim. Acta 56 (2011) 6089-6160.[12] F. Varmaghani, D. Nematollahi, Electrochemical study of 1,2-dihydropyridazine- 3,6-dione in protic and aprotic solvents: oxidative ring cleavage and reduction, Electrochim. Acta 56 (2011) 6089-6160.
-
-
扫一扫看文章
计量
- PDF下载量: 0
- 文章访问数: 1639
- HTML全文浏览量: 47

下载: