[
[1]. H. Schiff, H. Schiff, Mittheilungen aus dem Universitäts laboratorium in Pisa: Eine neue Reihe organischer Basen, J. Liebigs Annal. Chem. 131(1864) 118-119.
]Search in Google Scholar
[
[2]. A.A.A. Abu-Hussen, Synthesis and spectroscopic studies on ternary bis-Schiff-base complexes having oxygen and/or nitrogen donors, J. Coord. Chem. 59 (2006) 157-176.10.1080/00958970500266230
]Search in Google Scholar
[
[3]. K. Singh, M. S. Barwa, P. Tyagi, Synthesis and characterization of cobalt(II), nickel(II), copper(II) and zinc(II) complexes with Schiff base derived from 4-amino-3-mercapto-6-methyl-5-oxo-1,2,4-triazine, Eur. J. Med. Chem. 42 (2007) 394-402.10.1016/j.ejmech.2006.10.016
]Search in Google Scholar
[
[4]. P. Vicini, A. Geronikaki, M. Incerti, B. Busonera, G. Poni, C. A. Cabras, P. L. Colla, Synthesis and biological evaluation of benzo[d]isothiazole, benzothiazole and thiazole Schiff bases, Bioorg. Med. Chem. 11 (2003) 4785-478910.1016/S0968-0896(03)00493-0
]Search in Google Scholar
[
[5]. S. M. Sondhi, N. Singh, A. Kumar, O. Lozach, L. Meijer, Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some Schiff’s bases, Bioorg. Med. Chem. 14 (2006) 3758-3765.10.1016/j.bmc.2006.01.05416480879
]Search in Google Scholar
[
[6]. L. Cheng, J. Tang, H. Luo, X. Jin, F. Dai, J. Yang, Y. Qian, X. Li and B. Zhou, Antioxidant and antiproliferative activities of hydroxyl-substituted Schiff bases, Bioorg. Med. Chem. Lett. 20 (2010) 2417-2420.10.1016/j.bmcl.2010.03.03920346660
]Search in Google Scholar
[
[7]. B. Narayana, B. V. Ashalatha, K. K. V. Raj, N. S. Kumari, Synthesis of 3-amino-2-methyl/ethyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-d] pyrimidin-4(3H)-one and its Schiff bases as possible antimicrobial and non-steroidal antiinflammatory agents, Ind. J. Chem. 45B (2006) 2696-2703.10.1002/chin.200714171
]Search in Google Scholar
[
[8]. N. Sinha, S. Jain, A. Tilekar, R. S. Upadhayaya, N. Kishore, G. H. Jana, S. K. Arora, Synthesis of isonicotinic acid N’-arylidene-N-[2-oxo-2-(4-arylpiperazin-1-yl)-ethyl]-hydrazides as antituberculosis agents, Bioorg. Med. Chem. Lett. 15 (2005) 1573-1576.10.1016/j.bmcl.2005.01.07315745799
]Search in Google Scholar
[
[9]. J. Patole, D. Shingnapurkar, S. Padhyea, C. Ratledge, Schiff base conjugates of paminosalicylic acid as antimycobacterial agents, Bioorg. Med. Chem. Lett. 16 (2006) 1314-1317.10.1016/j.bmcl.2005.12.03516413184
]Search in Google Scholar
[
[10]. I. Kucukguzel, S. G. Kucukguzel, S. Rollas, G. O. Sanis, O. I. Ozdemir, T. Altug, J. Stables, Synthesis of some 3-(arylalkylthio)-4-alkyl/aryl-5-(4-aminophenyl)-4H-1, 2, 4-triazole derivatives and their anticonvulsant activity, IL Farmaco 59 (2004) 893-901.10.1016/j.farmac.2004.07.00515544794
]Search in Google Scholar
[
[11]. J. Wu, X. Liu, X. Cheng, Y. Cao, D. Wang, Z. Li, W. Xu, C. Pannecouque, M. Witvrouw, E. De Clercq, Synthesis of novel derivatives of 4-amino-3-(2-furyl)-5-mercapto-1,2,4-triazole as potential HIV-1 NNRTIs, Molecules 12 (2007) 2003-2016.10.3390/12082003614909217960101
]Search in Google Scholar
[
[12]. J. C. Menendez, M. P. Daiaz, C. Bellever, M. M. Sollhuber, Synthesis, anticonvulsant and antihypertensive activity of diastereomeric 9,10-dimethoxy-1,3,4,6,7,11b- hexa hydrospiro-[benzo(a)quinolizin-2,4-imidolidin]-2,5-diones, Eur. J. Med Chem. 27 (1992) 61-66.10.1016/0223-5234(92)90062-6
]Search in Google Scholar
[
[13]. M. T. Tarafder, A. Kasbollah, N. Saravan, K. A. Crouse, A. M. Ali, O. K. Tin, S-methyldithiocarbazate and its Schiff bases: evaluation of bondings and biological properties, Biochem. Mol. Biol. Biophy. 6 (2002) 85-91.10.1080/1025814029002720712186762
]Search in Google Scholar
[
[14]. R. Yadav, S. D. Srivastava, S. K. Srivastava, Synthesis, antimicrobial and antiflmmatory activities of 4-oxothiazolidine and their 5-arylidenes, Indian J. Chem, 44B, (2005)1262-1266. A. Kundu, N. A. Shakil, D. B. Saxena, J. P. Kumar, S. Walia, J. Environ. Sci. Health 44B (2000) 428.
]Search in Google Scholar
[
[15]. A. Kundu, N. A. Shakil, D. B. Saxena, J. P. Kumar, S. Walia, Microwave assisted solvent-free synthesis and biological activities of novel imines (Schiff bases), J. Environ. Sci. Health. 44B (2000) 428-434.10.1080/0360123090293464520183046
]Search in Google Scholar
[
[16]. H. Song, Y. Liu, L. Xiong, Y. Li, N. Yang, Q. Wang, Design, synthesis, and insecticidal evaluation of new pyrazole derivatives containing imine, oxime ether, oxime ester, and dihydroisoxazoline groups based on the inhibitor binding pocket of respiratory complex I, J Agric. Food Chem. 61 (2013) 8730-873610.1021/jf402719z23972278
]Search in Google Scholar
[
[17]. P. L. Olliaro, W. R. J. Taylor, Review, Antimalarial compounds: from bench to bedside, J. Experimental Biol. 206 (2003) 3753-3759.
]Search in Google Scholar
[
[18]. R. M. Issa, A. M. Khedr, H. Rizk, 1H NMR, IR and UV/VIS spectroscopic studies of some schiff bases derived from2-aminobenzothiazole and 2-amino-3-hydroxypyridine, Chin. Chem. Soc. 55 (2008) 875-884.10.1002/jccs.200800131
]Search in Google Scholar
[
[19]. A. W. Bauer, W. M. M. Kirby, J. C. Sherris, M. Truck, Antibiotic Susceptibility Testing by a Standardized Single Disk Method. Am. J. Clin. Pathol. 45 (1996) 493-498.
]Search in Google Scholar
[
[20]. R. Suresh, S. P. Sakthinathan, D. Kamalakkannan, K. Ranganathan, K. Sathiyamoorthi, V. Mala, R. Arulkumaran, S. Vijayakumar, R. Sundararajan, G. Vanangamudi, M. Subramanian, G. Thirunarayanan, G. Vanaja, P. Kanagambal, Solvent-free synthesis of azomethines, spectral correlations and antimicrobial activities of some E-benzylidene-4-chlorobenzenamines, Bull. Ethiop. Chem. Soc. 29 (2015) 275-290.10.4314/bcse.v29i2.10
]Search in Google Scholar
[
[21]. K. Ranganathan, D. Kamalakkannan, R. Suresh, S. P. Sakthinathan, R. Arulkumaran, R. Sundararajan, V. Manikandan, G. Thirunarayanan, Synthesis, Hammett spectral correlation and evaluation of antimicrobial activities of some substituted styryl 4′-piperidinophenyl ketones, Indian J. Chem. 58B (2019) 1131-1143.
]Search in Google Scholar
