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Synthesis and characterization of some new Schiff bases of 2-oxonaphtho[2,1-b][1,4]oxazine

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The literature review reveal that [1,4]-oxazine derivatives represent one of the most active classes of compounds possessing wide spectrum of biodynamic activities and use as potent therapeutic agents. In the present work, a series of Schiff base of 2-(2,3-dihydro-2-oxonaphtho[2,1-b][1,4]oxazin-1-yl)acetohydrazide, 5a-5j has been synthesized using 1-aminonaphthalen-2-ol. Various aromatic aldehyde were react with carbohydrazide 4 in the presence of acid to produce the 2-oxonaphtho[2,1-b][1,4]oxazin Schiff base derivatives with good yields. All synthesized compounds were characterized by IR, NMR and Mass spectrometry analysis.
Słowa kluczowe
Rocznik
Tom
Strony
26--30
Opis fizyczny
Bibliogr. 15 poz., tab., wz.
Twórcy
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
Bibliografia
  • [1] Y. Katsura, S. Nishino, H. Takasugi, Chem. Pharm. Bull. 11 (1991) 2937.
  • [2] N. Kajino, Y. Shibouta, K. Nishikawa, K. Meguro, Chem. Pharm. Bull. 11 (1991) 2896.
  • [3] R. Fringuelli, D. Pietrella, F. Schiaffella, A. Guarraci, S. Perito, F.Bistoni, A.Vecchiarelli, Bioorg. Med. Chem. 10 (2002) 1681.
  • [4] M. G. Nair, O. C. Salter, R. L. Kisliuk, Y. Gaumont, J. Med. Chem. 26 (1983) 1164.
  • [5] B. O. Buckman, R. Mohan, S. Koovakkat, Bioorg. Med. Chem. Lett. 8 (1998) 2235.
  • [6] E. Blattes, B. Lockhart, P. Lestage, L. Schwendimann, P. Gressens, M. B. Fleury, M. Largeron, J. Med. Chem. 48 (2005) 1282.
  • [7] K. M. Thaker, V.V Kachhadia, H.S. Joshi, Indian Journal Of Chemistry Section B, 42(6) (2003) 1544.
  • [8] Nirav M. Shah, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 6 (2014) 56-60.
  • [9] Piyush B. Vekariya, Jalpa R. Pandya, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 7 (2014) 45-52.
  • [10] Prakash Mehta, Prakash Davadra, Nirav Shah, Hitendra Joshi, International Letters of Chemistry, Physics and Astronomy 10 (2014) 74-80.
  • [11] Prakash Mehta, Prakash Dawedra, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 11(1) (2014) 1-8.
  • [12] S. M. S. Shariar, M. Jesmin, M. M. Ali, International Letters of Chemistry, Physics and Astronomy 7 (2014) 53-61.
  • [13] Mele Jesmin, M. Khairul Islam, Shaikh M. Mohsin Ali, International Letters of Chemistry, Physics and Astronomy 8 (2014) 64-72.
  • [14] Mallikarjun S. Yadawe, Shrishila N. Unki, Sangamesh A. Patil, International Letters of Chemistry, Physics and Astronomy 12 (2013) 94-104.
  • [15] Hirata Kazuyuki, et al. From PCT Int. Appl., 2007139002, 06 Dec 2007.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-6f997bb5-74ad-496d-84d8-d1053532e307
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