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2012 | 67 | 1-2 | 45-77
Tytuł artykułu

Solid Fly-ash:PTS catalyzed synthesis, spectral studies and antimicrobial activities of some 1,3-diarylpropenones

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The green catalyst Fly-ash:PTS has been prepared and characterized by IR and SEM analysis. Using this catalyst some aryl chalcones have been synthesized by aldol condensation of aryl methyl ketone and substituted benzaldehydes. It has been observed that this reaction yields more than 85% of the product. These chalcones have been characterized by their physical constants and spectral data following the procedures published in literature. The effect of substituents on the spectral data of the chalcones, synthesized, has been studied using single and multi-regression analysis with Hammett equation. The antibacterial and antifungal activities of these chalcones have been studied using Bauer-Kirby method.
Wydawca
Rocznik
Tom
67
Numer
1-2
Strony
45-77
Opis fizyczny
Daty
wydano
2012-12-01
online
2014-01-25
Twórcy
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram-608102, India
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram-608102, India
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram-608102, India
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram-608102, India
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram-608102, India
  • Department of Chemistry, Annamalai University, Annamalainagar-608002, India
autor
  • Department of Chemistry, Annamalai University, Annamalainagar-608002, India
Bibliografia
  • [1] G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran and K. Ravi, Indian J. Chem., 50B(4),593, (2011).
  • [2] G. Thirunarayanan, G. Vananagamudi, Arkivoc., 12, 58, (2006).
  • [3] G. Thirunarayanan, J. Indian Chem. Soc., 85, 447, (2008).
  • [4] G. Thirunarayanan, G. Vananagamudi, E-J. Chem., 4, 90, (2007).
  • [5] G. Thirunarayanan, Indian J. Chem., 46B, 1511, (2007).
  • [6] S. Kobayashi, H. Kiyohara and M. Yamaguchi, J. Am. Chem. Soc., 133, 708, (2011).
  • [7] W. Li, W. Wu, J. Yang, X. Liang, J. Ye, Synthesis., 1085, ( 2011).
  • [8] G.A. Morris and S.T. Nguyen, Tetrahedron Lett., 42, 2093, (2001).[Crossref]
  • [9] Z. Wang, L. Xu, Z. Mu, C. Xia, H. Wang, J. Mol. Catal., 218A, 157, (2004).
  • [10] S. H. Leung, S.A. Angel, J. Chem. Educ., 81, 1492, (2004).
  • [11] G. Thirunarayanan, J. Korean Chem. Soc., 52(4) 369, (2008).
  • [12] G. Thirunarayanan, P. Ananthakrishna Nadar, J. Indian Chem. Soc., 83(11) 1107, (2006).
  • [13] G. Thirunarayanan, P. Mayavel, K. Thirumurthy, Spectrochim Acta., 91A, 18, (2012).
  • [14] D.R. Palleros, J. Chem. Educ., 81(9), 1345, (2004).
  • [15] S.A. Basaif, T.R. Sobahi, A.K. Khalil, M.A. Hassan, Bull. Korean Chem. Soc., 26(11), 1677, (2005).
  • [16] Q. Xu, Z. Yang, D. Yin, F. Zhang, Catal. Commun., 9(1), 1579, (2008).
  • [17] P. Kumar, S. Kumar, K. Husain, A. Kumar, Chin. Chem. Lett., 22(1), 37, (2011).
  • [18] Z. Zhang, Y.W. Dong, G.W. Wang, Chem. Lett., 32(10), 966, (2003).
  • [19] H.E. Blackwell, Current Opinion in Chem. Biol., 10(3), 203, (2006).
  • [20] G. Thirunarayanan, “Proceedings of the 46th Annual convention of Chemists and International conference on recent research trends in chemical sciences” No. ORG OP5, p. C13, (2009).
  • [21] B. Krishnakumar, R. Velmurugan, M. Swaminathan, Catal. Commun., 12(5), 375, (2011).
  • [22] B.F.G. Johnson, J. Lewis, G.R. Stephenson, E.J.S. Vichi, J. Chem.Soc., Dalton Trans., 369 (1978).
  • [23] Kiadó, J. Thermal Anal. Calorimetry., 76, 193, (2010).
  • [24] Y. Xiuying, P. An-shun, J. Linyi Teachers Coll., 23, O621.3, 2004)
  • [25] P. Salehi, M. Dabiri, M. A. Zolfigol, M. A. B. Fard, J. Braz. Chem.Soc. 15(5), 773, (2004).
  • [26] D. Kamalakkannan, G. Vanangamudi, R. Arulkumaran, K. Thirumurthy, P. Mayavel, G.Thirunarayanan, Elixir Org. Chem., 46, 8251, (2012).
  • [27] P.T. Cardew, M.S. Ie, Chap. 2. Membrane technologies, pp. 2-20, (1998).
  • [28] R.J. Butcher, J.P. Jasinsky, B. Narayanan, K. Lakshmana, H.S. Yathirajan, Acta. Cryst., E64, o4919, (2008).
  • [29] Chem Spider Compound ID: 4650199.
  • [30] FRPSAX Farmaco, Edizione Scientifica., 25, 860, (1970).
  • [31] G. Vanangamudi, M. Subramanian , P. Jayanthi, R. Arulkumaran, D.Kamalakkannan, G. Thirunarayanan, Arab. J. Chem., doi:10. 1016/j.arabjc.2011.07.019[Crossref]
  • [32] G. Thirunarayanan, G. Vanangamudi, M. Subramanian, U. Umadevi, S. P. Sakthinathan, R. Sundararajan, Elixir Org. Chem., 39, 4643, (2011).
  • [33] M. Subramanian Ph.D. Thesis, Thiruvalluvar University, Vellore, 2011.
  • [34] C.G. Swain and E.C. Lupton Jr, J. Am Chem Soc., 90, 4328, (1968).[Crossref]
  • [35] M. Sivakumar, S. Phrabu Sreeneivasan, V. Kumar and M. Doble, Bioorg. Med. Chem. Lett., 17(10), 3169, (2007).
  • [36] K.L. Lahtchev, D.I. Batovska, St.P. Parushev, V.M. Ubiyvock, A.A.Sibirny, Eur.J. Med. Chem., 43(1), 1, (2008).
  • [37] V.S. Parmer, K.S. Bishit, R. Jain, S. Singh, S.K. Sharma, S. Gupta, S. Malhotra, O.D. Tyagi, A. Vardhan, H.N. Pati, D.V. Berghe, A.J. Vlietinek, Indian J. Chem., 35B, 220, (1996).
  • [38] G. Thirunarayanan, S. Surya, S. Srinivasan, G. Vanangamudi, V. Sathyendiran, Spectrochim Acta., 75A, 152, (2010). 39] G. Thirunarayanan, G. Vanangamudi, M. Subramanian, Elixir. Org.Chem., 43, 6987, (2012).
  • [40] J.N. Dominguez, C. Leon and J. Rodrigues, IL Farmaco., 60(4), 307, (2005).
  • [41] Y.M. Lin, Y. Zhon, M.T. Flavin, L.M. Zhon, W. Ne, F.C. Chen, Bioorg. Med. Chem., 10(8), 2795, (2002).
  • [42] J. Deng, T. Sanchez and Q.A.M. Lalith, Bioorg. Med. Chem., 15(14), 4985, (2007).[Crossref]
  • [43] M.W. Weber, L.A. Hunsaker, S.F. Abcouwer, L.M. Decker, D.L. Vander Jagat, Bioorg. Med. Chem., 13, 3811, (2005).
  • [44] W. Bauer, W.M. Kirby, J.C. Sherris, M. Truck, Am. J. Clin. Pathol., 45, 493, (1996).
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_v10063-012-0003-8
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