PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Infrared and NMR spectral Hammett correlations in 4-(2-naphthyl)-5,6-dihydro-6-(substituted phenyl)-4H-1,3-oxazine-2-amines

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series containing ten titled compounds have been synthesised and recorded the IR and NMR spectra. From the spectra the infrared νNH, C=N, C-O-C stretches, NMR chemical shifts of (δ, ppm) NH and C=N were assigned and correlated with Hammett substituent constants, F and R parameters using single regression analysis. From the results, the effects of substituent on the above spectral frequencies were discussed.
Rocznik
Tom
Strony
38--46
Opis fizyczny
Bibliogr. 30 poz., tab., wz.
Twórcy
  • Department of Chemistry, Annamalai University, Annamalainagar - 608 002, India
  • DDE Wing of Chemistry, Annamalai University, Annamalainagar - 608 002, India
autor
  • Department of Chemistry, National College, Tiruchirappalli - 620001, India
Bibliografia
  • [1] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9(2) (2013) 152-161.
  • [2] S. Vijayakumar, et al., International Letters of Chemistry, Physics and Astronomy 9(1) (2013) 68-86.
  • [3] G. Thirunarayanan, M. Gopalakrishnan, G. Vanangamudi, Spectrochim. Acta 67A (2007) 1106-1612.
  • [4] G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran, K. Ravi, Indian J. Chem. 50B(4) (2011) 593-604.
  • [5] G. K. Dass, Indian J. Chem. 40(A)(1) (2001) 23-29.
  • [6] Y. H. Wang, J. W. Zou, B. Zhang, Y. X. Lu, H. X. Jin, Q. S. Yu, J. Mol. Struct. (Theochem) 755(1-2) (2005) 31-37.
  • [7] V. Horváth, Z. Varga and A. Kovács, J. Mol. Struct. (Theochem) 755(1-3) (2005) 247-251.
  • [8] D. Kamalakkannan, G. Vanangamudi, R. Arulkumaran, K. Thirumurthy, P. Mayavel, G. Thirunarayanan, Elixir Org. Chem. 46 (2012) 8157-8166.
  • [9] G. Thirunarayanan, R. Arulkumaran, R. Sundararajan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 82-97.
  • [10] B. P. Mathew, A. Kumar, S. Sharma, P. K. Shukla, M. Nath, Euro. J. Med. Chem. 45 (2010) 1502-1507.
  • [11] M. J. Elarfi, H. A. Al-Difar, Sci. Rev.Chem. Commun. 2(2) (2012) 103-107.
  • [12] V. Tiwari, J. Meshram, P. Ali, J. Sheikh, U. Tripathi, J. Enzyme Inhibit. Medi. Chem. 26(4) (2011) 569-578.
  • [13] B. C. Das, A. V. Madhukumar, J. Anguiano, S. Mani, Bioorg. Med. Chem. Lett. 19(15) (2009) 4204-4206.
  • [14] D. Zhou, B. L. Harrison, U. Shah, T. H. Andree, G. A. Hornby, R. Scerni, Bioorg. Med. Chem. Lett. 16(5) (2006) 1338-1341.
  • [15] S. Wang, Y. Li, Y. Liu, A. Lu, Q. You, Bioorg. Med. Chem. Lett. 18(14) (2008) 4095-4097.
  • [16] Y. Ando, K. Ando, M. Yamaguchi, J. Kunitomo, M. Koida, R. Fukuyama, Bioorg. Med. Chem. Lett. 16(22) (2006) 5849-5854.
  • [17] L. Benameur, Z. Bouaziz, P. Nebois, M. H. Bartoli, M. Boitard, H. Fillion, Chem. Pharm. Bull. 44(3) (1996) 605-608.
  • [18] K. Roy, I. Mitra, A. Saha, Chem. Biol. Drug Design 74(5) (2009) 507-516.
  • [19] A. Blaser, D. Palmer, S. H. Sutherland, I. Kmentova, S. G. Franzblau, B. Wan, J. Med. Chem. 55(1) (2012) 312-326.
  • [20] L. Seal, D. Von Hoff. R. Lawrence, E. Izbicka, R. M. Jamison, Invest. New Drug 15(4) (1997) 289-296.
  • [21] B. Brudeli, L. R. Moltzau, K. W. Andressen, K. A. Krobert, J. Klaveness, F. O. Levy, Bioorg. Med. Chem. Lett. 18(24) (2010) 8600-8613.
  • [22] M. Akhter, A. Husain, N. Akhter, M. S.Y. Khan, Indian J. Pharm. Sci. 73 (2011) 101-104.
  • [23] D. Gothi, J. M. Joshi, Recent Patent. Antiinfect. Drug Discovery 6(1) (2011) 27-37.
  • [24] G. Thirunarayanan, V. Renuka, K. G. Sekar, K. Lakshmanan, K. Anbarasu, International Letters of Chemistry, Physics and Astronomy 4 (2014) 66-81.
  • [25] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 109-116.
  • [26] G. Thirunarayanan, K. G. Sekar, Der Pharma Chemica 5(6) (2013)142-148.
  • [27] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
  • [28] G. Thirunarayanan, M. Suresh, International Letters of Chemistry, Physics and Astronomy 4 (1) (2014) 1-11.
  • [29] G. Thirunarayanan, K. G. Sekar, J. Saudi Chem. Soc. (2013); DOI: 10.1016/j.jscs.2013.12.002.
  • [30] C. G. Swain, E. C. Lupton Jr, J. Am. Chem. Soc. 90 (1968) 4324-4337.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f52a816b-30b7-4feb-a25d-31eab810db07
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.