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Hammett spectral correlations in some aryl 1,3-oxazine-4-thione derivatives

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of some aryl 1,3-oxazine-4-thione derivatives have been synthesized by 1-methyl imidazole catalyzed three component one pot synthetic method in room temperature. The purities of these thiones were studied by their physical constants and spectroscopic data. The infrared and 13C NMR spectral data of CN and CS were correlated with Hammett substituent constants, F and R parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituent on the spectral data was studied.
Rocznik
Strony
193--200
Opis fizyczny
Bibliogr. 46 poz., tab., wz.
Twórcy
  • Department of Chemistry, Annamalai University, Annamalainagar - 608 002, India
autor
  • Department of Chemistry, National College, Tiruchirappalli - 620 001, India
Bibliografia
  • [1] D. A. Brown, C. J. Powers, Bioorg. Med. Chem. 3 (1995) 1091-1097.
  • [2] M. Gutschow , L. Kuerschner, U. Neumann, M. Pietsch, R. Loser, N. Koglin, K. Eger, J. Med. Chem. 42 (1999) 5437-5447.
  • [3] A. N. Mayekar, H. S. Yathirajan, B. Narayana, B. K. Sarojini, N. Suchetha Kumari and W. T. A. Harrison, Int. J. Chem. 3 (1) (2011) 74-86.
  • [4] G. R. Madhavan, R. Chakrabarti, K. A. Reddy, B. M. Rajesh, V. Balaju, P. B. Rao, R. Rajagopalan, J. Iqbal, Bioorg. Med. Chem. 14 (2006) 584-591
  • [5] K. Balbir, K. Ramandeep, Arkivoc. 15 ( 2007) 315-323
  • [6] P. W. Hsieh, R. F. Chang, H. C. Chang, W. P. Cheng, C. L. Chiang, L. F. Zeng, K. H. Lin, C. Y. Wu, Bioorg. Med. Chem. Lett. 14 (2004) 4751-4754
  • [7] K. Waisser, J. Gregor, L. Kubikova, V. Klimesova, J. Kunes, M. Machacek, J. Kaustova, Eur. J. Med. Chem. 35 (2000) 733-741
  • [8] P. W. Hsieh, T. L. Hwang, C. C. Wu, F. R. Chang, T. W. Wang, Y. C. Wu, Bioorg. Med. Chem. Lett. 15 (2005) 2786-2789
  • [9] J. C. Kern, E. A. Terefenko, A. Fensome, R. Unwalla, J. Wrobel, Y. Zhu, J. Cohen, R. Winneker, Z. Zhang, P. Zhang, Bioorg. Med. Chem. Lett. 17 (2007) 189-192
  • [10] A. Bolognese, G. Correale, M. Manfra, A. Lavecchia, O. Mazzoni, E. Novellino, V. Barone , P. La Colla, R. Loddo, J. Med. Chem. 45 (2002) 5217-5223
  • [11] R. L. Jarvest , S. C. Connor, J. G. Gorniak, L. J. Jennings, H. T. Serafinowska and A. West., Bioorg. Med. Chem. Lett. 7 (1997) 1733-1738
  • [12] E. Colson, J. Wallach and M. Hauteville, Biochimie 87(2005)223-230
  • [13] P. J. Atkinson, et al., Bioorg. Med. Chem. Lett. 15 (2005) 737-741
  • [14] G. Thirunarayanan, M. Gopalakrishnan, G. Vanangamudi, Spectrochim. Acta 67A (2007) 1106-1612.
  • [15] A. Perjessy, M. Laucova, Coll. Czech. Chem. Commun. 36 (1971) 2944-22950. [16] W. F. Winecoff, D. W. Boykin Jr., J. Org. Chem. 37 (4) (1972) 676.
  • [17] G. Thirunarayanan, P. Ananthakrishna Nadar, Asian J. Chem. 14(3-4) (2002) 1518-1522.
  • [18] D. Seebach, R. Gilmour, U. Grosˇelj, G. Deniau, C. Sparr, M. O. Ebert, A. K. Beck, Helvi. Chem. Acta. 93 (2010) 603-634.
  • [19] T. A. Foglia, P. A. Barr and M. J. Idacavage, J. Org. Chem. 41 (1976) 3452-3455.
  • [20] V. Všetečka, J. Pecka, M. Procházka, Collect. Czech. Chem. Commun. 47 (1982) 277-285.
  • [21] G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran, K. Ravi, Indian J. Chem. 50B(4) (2011) 593-604.
  • [22] G. Thirunarayanan, P. Mayavel, K. Thirumurthy, S. Dineshkumar, R. Sasikala, P. Nisha, A. Nithyaranjani, European Chem. Bull. 2(9) (2013) 598-605.
  • [23] K. Rajasekharan, C. Gnansekaran, J. Chem. Soc. Perkin Trans II (1987) 263-266.
  • [24] K. Rajasekharan, C. Gnansekaran, Indian J. Chem. 25A (1986) 64-66.
  • [25] V. Mala, K. Sathiyamoorthy, S. P. Sakthinathan, D. Kamalakkannan, R. Suresh, G. Vanangamudi, G. Thirunarayanan, Q-Science Connect, 2013:7; DOI http://dx.doi.org/10.5339,2013.7
  • [26] G. Vanangamudi, M. Subramanian, P. Jayanthi, R. Arulkumaran, D. Kamalakkannan G. Thirunarayanan, Arabian J. of Chemistry, (2011). doi:10.1016/j.arabjc.2011.07.019
  • [27] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 109 116.
  • [28] G. Thirunarayanan, K.G. Sekar, R. Lakshmi Narayanan, International Letters of Chemistry, Physics and Astronomy 13(1) (2014) 88-94.
  • [29] M. A. Khalilzadeh, I. Yavari, Z. Hossaini and H. Sadeghifar, Monastch Chem. 140 (2009) 467-471.
  • [30] R. Arulkumaran, S. Vijayakumar, R. Sundararajan, S. P. Sakthinathan, D. Kamalakkannan, R. Suresh, K. Ranganathan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2012) 17-38.
  • [31] G. Thirunarayanan, K. Ravi, International Letters of Chemistry, Physics and Astronomy 14 (2013) 44-57.
  • [32] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9(2) (2013) 152-161.
  • [33] S. P. Sakthinathan, G. Vanangamudi, G. Thirunarayanan, Spectrochim. Acta 95A (2012) 693 700.
  • [34] S. P. Sakthinathan, R. Suresh, V. Mala, K. Sathiyamoorthi, D. Kamalakkannan, K. Ranganathan, S. John Joseph, G. Vanangamudi, G. Thirunarayanan, Int. J. Sci. Res. Know. 1(11) (2013) 472-483.
  • [35] 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. 101A (2013) 239-248.
  • [36] G. Thirunarayanan, K. Sekar, Organic Chem: An Indian J. 9(12) (2013) 483-492.
  • [37] G. Thirunarayanan, M. Suresh, International Letters of Chemistry, Physics and Astronomy 1 (2014) 67-73.
  • [38] P. Janaki, K. G. Sekar, G. Thirunarayanan, Journal of Saudi Chem. Soc. (2012) Doi.10.1016/j.jscs.2012.11.013
  • [39] G. Vanangamudi, M. Subramanian, G. Thirunarayanan, Arabian J. Chem. (2013) DOI: 10.1016/j.arabjc.2013.03.006,
  • [40] M. Subramanian, G. Vanangamudi, G. Thirunarayanan, Spectrochim. Acta 110A (2013) 116 123.
  • [41] G. Thirunarayanan, G. Vanangamudi, M. Subramanian, Organic Chemistry: An Indian J 9(1) (2012)1-16.
  • [42] Swain C. G., Lupton E. C. Jr., J. Am. Chem. Soc. 90 (1968) 4328-4337.
  • [43] G. Thirunarayanan, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 10(1) (2013) 18-34.
  • [44] K. G. Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 8(3) (2013) 249-258
  • [45] S. Vijayakumar, R. Arulkumaran, R. Sundararajan, S. P. Sakthinathan, R. Suresh, D. Kamalakkannan, K. Ranganathan, K. Sathiyamoorthi, V. Mala, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9(1) (2013) 68-86.
  • [46] S. P. Sakthinathan, R. Suresh, V. Mala, K. Sathiyamoorthi, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, S. Vijayakumar, R. Sundararajan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 6 (2013) 77-90.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-a2cfc23a-3bdf-4b08-bfc3-00dc60119b62
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