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Spectral QSAR and QPR study of some (E)-4-(((2 hydroxy-6-(substituted phenyl)-1,6 dihydropyrimidin 4-yl)methyl)diazenyl)benzoic acid derivatives

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of titled compounds were synthesized and recorded the infrared and NMR spectra. The assigned spectral group frequencies were correlated with Hammett substituent constants, F and R parameter. From the statistical analysis results, the effect of substituents on the spectral group frequencies has been studied.
Rocznik
Strony
10--20
Opis fizyczny
Bibliogr. 23 poz., wykr., wz.
Twórcy
  • Department of Chemistry, Annamalai University, Annamalainagar - 608 002, India
autor
  • Department of Chemistry, National College, Tiruchirappalli - 620 001, India
Bibliografia
  • [1] (a). L. J. Liu, J. H. Hong, Nucleos. Nucleot. Nucl. Acid. 28(4) (2009) 303-314; (b). H. O. Kim, S. K. Ahn, A. J. Alves, J. W. Beach, L. S. Jeong, B.G. Choi, P. Van Roey, R. F. Schinazi, C. K. Chu, J. Med. Chem. 35(11) (1992) 1987-1995; (c). E. M. Sharshira, N. M. M. Hamada, Amer. J. Org. Chem. 2(2) (2012) 26 31.
  • [2] A. V. Saranys, S. Rani, J. Pharm. Res. 5(2) (2012) 1098-1101.
  • [3] V. L. Rusinov, T. L. Pilicheva, O. N. Chupakhin, G. V. Kovalev, E. R. Komina, Pham. Chem. J. 20(8) (1986) 550-554.
  • [4] P. Herdewijn, J. Balzarini, M. Baba, R. Pauwels, A. Van Aerschot, G. Janssen, E. De Clercq, J. Med. Chem. 31(10) (1988) 2040-2048.
  • [5] M. Cozzi, F. Giorgi, E. Marcelli, F. Pentimalli, I. M. Forte, S. Schenone, V. D’Urso, G. De Falco, M. Botta, A. Giordano, P. Indovina, Cell Cycle 11(5) (2012) 1029-1039.
  • [6] Z. M. Nofa, H. H. Fahmy, E. S. Zarea, W. El-Eraky, Acta Pol. Chem. 68(4) (2011) 507-517.
  • [7] S. B. Mohan, B. V. Ravi Kumar, S. C. Dinda, D. Naik, S. Prabu Seenivasan, V. Kumar, D. N. Ranan, P. S. Brahmkshatriya, Bioorg. Med. Chem. Lett. 22924 (2012) 7539-7542.
  • [8] J. Majeed, M. Shaharyar, J. Enzyme Inhib. Med. Chem. 26(6) (2011) 819-826.
  • [9] O. A. Fathalla, H. H. RAdwan, S. M. Awad, M. S. Mohammed, Indian J. Chem. 54B (2006) 980-986.
  • [10] S. I. Pretorius, W. J. Breytenbach, C. De Kocj, P. J. Smith, D. D. N’Da, Bioorg. Med. Chem. 21(1) (2013) 269-277.
  • [11] K. Sathiyamoorthi, V. Mala, R. Suresh, S. P. Sakthinathan, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, R. Sundararajan, S. Vijayakumar, G. Vanangamudi, G. Thirunarayanan, Der Pharma Chemica 6(1) (2014) 97-110.
  • [12] G. Thirunarayanan, S. Pazhamalai, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 8 (2014) 38-46.
  • [13] G. Thirunarayanan, K. G. Sekar, J. Taibah Univ. Sci. 8 (2014) 124-136.
  • [14] S. P. Sakthinathan, R. Suresh, V. Mala, K. Sathiyamoorthy, D. Kamalakkannan, K. Ranganathan, S. John Joseph, G. Vanangamudi, G. Thirunarayanan, Int. J. Sci. Res. Know. 1(11) (2013) 472-483.
  • [15] G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran, K. Ravi, Indian J. Chem. 50B(4) (2011) 593-604.
  • [16] S. John Joseph, D. Kamalakkannan, R. Arulkumaran, S. P. Sakthinathan, R. Suresh, R. Sundararajan, S. Vijayakumar, K. Ranganathan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 99-123.
  • [17] S. Groothuys, S. A. M.W. Van de Broek, B. H. M. Kuijpers, M. IJsselstijn, F. L. van Delft, F. P. J. T. Rutjes, Synlett. (2008) 111-115.
  • [18] P. Janaki, K. G. Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9 (2014) 16-22.
  • [19] P. Mayavel, K. Thirumurthy, S. Dineshkumar, G. Thirunarayanan, Q. Sci. Connect. 11 (2014).
  • [20] V. Sathiyendiran, K. G. Sekar, G. Thirunarayanan, R. Arulkumaran, R. Sundararajan, D. Kamalakkannan, R. Suresh, V. Manikanadan, R. Vijayakumar, G. Vanangamudi, International Letters of Chemistry, Physics and Astronomy 11(1) (2014) 33-43.
  • [21] N. Kalyanasundaram, S. P. Sakthinathan, R. Suresh, D. Kamalakkannan, S. John Joseph, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9 (2014) 23-47.
  • [22] A. R. Trivedi, D. K. Dodiya, N. R. Ravat, V. H. Shah, Arkivoc. 11 (2008) 131-141.
  • [23] Swain C. G., Lupton Jr., E. C. J. Am. Chem. Soc. 90 (1968) 4328-4337.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-c6353eea-2761-4be9-bb19-16a42a3a1170
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