Quinolone antibacterials. 2. 6??Substituted??7??(2??thiazolyl and thiazolidinyl) quinolones
…, A Haemers, D Vanden Berghe…
Index: Zhang; Haemers; Vanden Berghe; Pattyn; Bollaert; Levshin Journal of Heterocyclic Chemistry, 1991 , vol. 28, # 3 p. 685 - 695
Full Text: HTML
Citation Number: 16
Abstract
Abstract A series of 6-substituted-1-ethyl-1, 4-dihydro-4-oxo-7-(2-thiazolyl-and thiazolidinyl) quinoline-3-carboxylic acids were synthesized. Substitution at the 6-position was H, F or Cl. The Hantzsch method was used for the preparation of the thiazolylquinolones. The thiazolidinylquinolones were synthesized by quaternization of the corresponding thiazolyl analogues, followed by reduction of the obtained thiazolium salts with sodium borohydride ...
Related Articles:
[Kim, Byeong Hyo; Han, Rongbi; Piao, Fengyu; Jun, Young Moo; Baik, Woonphil; Lee, Byung Min Tetrahedron Letters, 2003 , vol. 44, # 1 p. 77 - 79]
[Mali, Sachitanand M.; Bhaisare, Rupal D.; Gopi, Hosahudya N. Journal of Organic Chemistry, 2013 , vol. 78, # 11 p. 5550 - 5555]
[Bogert; Beans Journal of the American Chemical Society, 1904 , vol. 26, p. 492]
[Bogert; Beans Journal of the American Chemical Society, 1904 , vol. 26, p. 492]
[Bogert; Beans Journal of the American Chemical Society, 1904 , vol. 26, p. 492]