PL EN


Preferences help
enabled [disable] Abstract
Number of results
2014 | 69 | 1-2 |
Article title

Perchloric Acid Catalyzed Condensation of Amine and Aldehydes: Synthesis and Antibacterial Activities of Some Aryl (E)-Imines

Content
Title variants
Languages of publication
EN
Abstracts
EN
A series of Schiff’s bases (aryl E-imines) have been derived from the perchloric acid catalyzed condensation of aryl amines and substituted benzaldehydes. The yield of the Schiff’s bases are more than 80%. The synthesized Schiff’s bases are characterized by their physical constants, analytical and spectroscopical data. The antibacterial activities of these Schiff’s bases have been studied using Bauer-Kirby method.
Keywords
Year
Volume
69
Issue
1-2
Physical description
Dates
published
2014
online
23 - 05 - 2015
References
  • K.Y. Lau, A. Mayr, K.K. Cheung, Inorg. Chim. Acta, 285, 223, (1999).
  • A.S. Shawali, N.M.S. Harb, K.O. Badahdah, J. Heterocycl. Chem., 22, 1397, (1985).
  • S. France, M.H. Shah, A. Weatherwax, H. Wack, J.P. Roth, T. Lectka, J. Am. Chem. Soc., 127, 1206, (2005).
  • C.K.Z. Andrade, S.C.S. Takeda, L.M. Alves, J.P. Rodrigues, P.A.Z. Suarez, R.F. Brandao, V.C.D. Soares, Synlett, 12, 2135, (2004).
  • M. Abid, M. Savolainen, S. Landge, J. Hu, G.K. Surya Prakash, G.A. Olah, B. Torok, J. Fluorine Chem., 128, 587, (2007).
  • D.A. Barr, G. Donegn, R. Grigg, J. Chem. Soc. Perkin Trans. 1, 1550, (1989).
  • L. Blackburn, R.J.K. Taylor, Org. Lett., 3, 1637, (2001).
  • M. Gopalakrishnan, P. Sureshkumar, V. Kanagarajan, J. Thanusu, J. Res. Chem. Intermed., 33, 541, (2007). [9] R.T. McBurney, F. Portela-Cubillo, J.C. Walton, RSC Adv., 2, 1264, (2012).
  • A.K. Chakraborti, S. Bhagat, S. Rudrawar, Tetrahedron Lett., 45, 7641, (2004).
  • R.S. Varma, Green Chem., 1, 43, (1999).
  • A. Hasaninejad, A. Zare, H. Sharghi, M. Shekouhy, Arkivoc, 11, 64, (2008).
  • C.M. Bode, A. Ting, S.E. Schaus, Tetrahedron, 62, 11499, (2006).
  • M.A. Vazquez, M. Landa, L. Reyes, M.J. Tamariz, D. Francisco, Synth. Commun., 34, 2705, (2004).
  • M. Hudlicky, Oxidations in Organic Chemistry, ACS Monograph Series 186, American Chemical Society, Washington DC, (1990), p. 174.
  • S.M. Landge, V. Atanassova, M. Thimmaiah, B. Torok, Tetrahedron Lett., 48, 5161, (2007).
  • A. Kundu, N.A. Shakil, D.B. Saxena, J. Pankaj Kumar, S. Walia, J. Environ. Sci. Health B, 44, 428, (2009).
  • S.F. Martin, Pure Appl. Chem., 81, 195, (2009).
  • S.E. Denmark, G.L. Beutner, Angew. Chem. Int. Ed., 47, 1560, (2008).
  • P.K. Kabada, J. Heterocycl. Chem., 12, 143, (1975).
  • P.K. Kabada, J. Med. Chem., 31, 196, (1998).
  • D. Bandyopadhyay, S. Mukherjee, R.R. Rodriguez, B.K. Banik, Molecules, 15, 4207, (2010).
  • V. Tiwari, J. Meshram, P. Ali, Der. Pharm. Chem., 2, 187, (2010).
  • M. Sayyed, S. Mokle, M. Bokhare, A. Mankar, S. Surwase, S. Bhusare, Y. Vibhute, Arkivoc, 2, 187, (2006).
  • A.A. Bakibaev, V.K. Gorshkova, O.V. Arbit, V.D. Filimonov, A.S. Saratikov, Pharm. Chem. J., 28, 335, (1994).
  • S. Kantevari, T. Yempala, P. Yogeeswari, D. Sriram, B. Sridhar, Bioorg. Med. Chem. Lett., 21, 4316, (2011).
  • R. Yadav, S.D. Srivastava, S.K. Srivastava, Indian J. Chem., 44B, 1262, (2005).
  • B.W. Bauer, W.M.M. Kirby, J.C. Sherris, M. Truck, Am. J. Clin. Pathol., 45, 493, (1966).
  • R. Suresh, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, R. Sundararajan, S.P. Sakthinathan, S. Vijayakumar, K. Sathiyamoorthi, V. Mala, G. Vanangamudi, K. Thirumurthy, P. Mayavel, G. Thirunarayanan, Spectrochim. Acta A, 101, 239, (2013).
Document Type
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.ojs-doi-10_17951_aa_2014_69_1-2_159
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.