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Hammett spectral correlations in benzofuranyl flavonols

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series containing eleven benzofuranyl flavonols have been prepared by cyclization of 3-hydroxybenzofuranyl chalcones with 30 % hydrogen peroxide in the presence of sodium bicarbonate. The synthesized flavonols were characterized by their physical constants, analytical and spectroscopic data. The infrared spectral νOH, CO stretches(cm-1), NMR chemical shifts of OH, CO(δ, ppm) of these flavonols were assigned and correlated with Hammett substituent constants, F and R parameters using single and multi linear regression analysis. From the results of statistical analyses, the effects of substituents on the above group frequencies were discussed.
Rocznik
Tom
Strony
39--47
Opis fizyczny
Bibliogr. 20 poz., tab., wz.
Twórcy
  • Department of Chemistry, Annamalai University, Annamalainagar - 608002, Tamil Nadu, India
autor
  • Department of Chemistry, National College, Tiruchirrappalli - 620001, Tamil Nadu, India
Bibliografia
  • [1] G. Thirunarayana, P. Ananthakrishna Nadar, Asian J. Chem. 14(3-4) (2002) 1518-1522.
  • [2] W. F. Winecoff, D. W. Boykin Jr., J. Org. Chem. 37 (4) (1972) 676.
  • [3] A. Perjessy, M. Laucova, Coll. Czech. Chem. Commun. 36 (1971) 2944-22950.
  • [4] T. A. Foglia, P. A. Barr, M. J. Idacavage, J. Org. Chem. 41 (1976) 3452-3455.
  • [5] (a) V. Všetečka, J. Pecka and M. Procházka, Collect. Czech. Chem. Commun. 47 (1982) 277-285.
  • (b) G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran, K. Ravi, Indian J. Chem. 50B(4) (2011) 593-604.
  • [6] G. Thirunarayanan, M. Gopalakrishnan, G. Vanangamudi, Spectrochim. Acta. 67A (2007) 1106-1612.
  • [7] G. Thirunarayanan, K. G. Sekar, J. Taibah Univ. Sci. 2013. DOI: 10.1016/j.jtusci.2013.11.003.
  • [8] S. John Joseph, R. Arulkumaran, D. Kamalakkannan, S. P. Sakthinathan, R. Sundararajan, R. Suresh, S. Vijayakumar, K. Ranganathan, N. Kalyanasundaram, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 48-65.
  • [9] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
  • [10] 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.
  • [11] K. G. Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 8(2) (2013) 160-174.
  • [12] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 109-116.
  • [13] D. Kamalakkannan, G. Vanangamudi, R. Arulkumaran, K. Thirumurthy, P. Mayavel, G. Thirunarayanan, Elixir Org. Chem. 46 (2012) 8157-8166.
  • [14] P. M. G. Samy, Y. R. Prasad, B. S. Sastry, D. Giles, M. Gurumurthy, Y. S. Agasimundin, Der Pharm. Chem 5 (2013) 8-13.
  • [15] M. Subramanian, G. Vanangamudi, G. Thirunarayanan, Spectrochim Acta 110A (2013) 116-123.
  • [16] K. G Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 8(3) (2013)249-258.
  • [17] K. Sathiyamoorthy, V. Mala, S.P. Sakthinathan, D. Kamalakkannan, R. Suresh, G. Vanangamudi, G. Thirunarayanan, Spectrochim. Acta 112A (2013) 245-256.
  • [18] 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.
  • [19] G. Thirunarayanan, M. Suresh, International Letters of Chemistry, Physics and Astronomy 4 (1) (2014) 1-11.
  • [20] C. G. Swain, E. C. Lupton Jr., J. Am. Chem. Soc. 90 (1968) 4328-4337.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-14c2ef8a-f394-4700-9939-981b266f8a5b
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