Tytuł artykułu
Autorzy
Wybrane pełne teksty z tego czasopisma
Identyfikatory
Warianty tytułu
Języki publikacji
Abstrakty
On pursuing research about [1,2,4] triazolo [4,3-a] quinoxaline, in this paper we report a small library of novel class of [1,2,4] triazolo [4,3-a] quinoxaline derivatives containing pyridinyl thiazole moiety. Particularly valuable features of this method include high yield, broad substrate scope, shorter reaction time and straightforward procedure. The structures of new compounds have been characterized on the basis of elemental analysis, FT-IR, 1H NMR, 13C NMR, and mass spectral data.
Słowa kluczowe
Rocznik
Tom
Strony
63--73
Opis fizyczny
Bibliogr. 25 poz., tab., wz.
Twórcy
autor
- Department of Chemistry, Saurashtra University, Rajkot-360005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot-360005, Gujarat, India
Bibliografia
- [1] Xuan X., Zhiguang X., Xiang L., Weihua L., J. Med. Chem. 11 (2001) 317.
- [2] Zitouni G., Kaplancıklı Z. A., Yıldız M. T., Chevallet P., Eur. J. Med. Chem. 40 (2005)607.
- [3] Demirbas N., Karaoglu S. A., Demirbas A., Sanak K., Eur. J. Med. Chem. 39 (2004) 793.
- [4] Kane J. M., Baron B. M., Dudley M. W., Sorensen S. M., Staeger M. A., Millar F. P., J. Med. Chem. 33 (1990) 2772.
- [5] Holla B. S., Veerendra B., Shivananada M. K., Pujari B., Eur. J. Med. Chem. 28 (2003) 759.
- [6] Tozkoparan B., Kupeli E., Yesilada E., Ertan M., Bioorg. Med. Chem. 15 (2007) 1808.
- [7] Holla B. S., Veerendra B., Shivananada M. K., Pujari B., Eur. J. Med. Chem. 38 (2003) 759.
- [8] Abdel-Aal M. T., El-Sayed W. A., El-Kosy S. M., El-Ashry E. S. H., Arch. Pharm. Chem. Life Sci. 341 (2008) 307.
- [9] Chai B., Qian X., Cao S., Liu H., Song G., Arkivoc. 2 (2003) 141.
- [10] Modzelewska-Banachiewicz B., Banachiewicz J., Chodkowska A., Jagiello-Wojtowicz E., Eur. J. Med. Chem. 39 ( 2004) 873.
- [11] Jaso A., Zarranz B., Aldana I., Monge A., J. Med. Chem. 48 (2005) 2019.
- [12] Sarges R., Howard H. R., Browne R. G., Lebel, L. A., Seymour P. A., Koe B. K., J. Med. Chem. 33 (1990) 2240.
- [13] Dailey S., Feast J. W., Peace R. J., Sage I. C., Till S., Wood E. L., J. Mater. Chem. 11 (2001) 2238.
- [14] Bayoumi A., Ghiaty A., El-Morsy A., Abul-Khair H., Hassan B., Bulletin of Faculty of Pharmacy, Cairo University. 50 (2012) 141.
- [15] Chowdary K., et al., Indian Journal of Chemistry. 38B (1999) 1371.
- [16] Antonino L., Guarcello A., Tetrahedron Letters. 49 (2008) 1847.
- [17] Catarzi D., Colotta V., Varano F., J. Med. Chem. 48 (2005) 7932.
- [18] Kondapalli V., Rao V., Kumar D., Bull. Korean Chem. Soc. 32 (2011) 8.
- [19] Dodson R. M., King L. C., J Am Chem Soc. 67 (1945) 2242.
- [20] Khunt H., Pipaliya P., Ghelani S., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 24 (2014) 134.
- [21] Patel A. S., Khunt H., Babariya J., Ghelani S., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 30 (2014) 106.
- [22] Gami P., Vilapara K., Khunt H., Babariya J., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 30 (2014) 127.
- [23] Khunt H., Babariya J., Dedakiya C., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 30 (2014) 185.
- [24] Khunt H., Babariya J., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 31 (2014) 20.
- [25] Prajapati D., Vilapara K., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 33 (2014) 12.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-97f75ca5-5fcc-4baa-89ec-0d3337c38814