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Synthesis and Antibacterial Activity of Some Oxazolone Derivatives
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 Title & Authors
Synthesis and Antibacterial Activity of Some Oxazolone Derivatives
Aaglawe M. J.; S. S. Dhule; S. S. Bahekar; P. S. Wakte; D. B. Shinde;
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 Abstract
A series of oxazolone derivatives (4a-n) have been synthesized as a potential antibacterial agent. Titled compounds have been prepared by the condensation of aryloxy acetyl-amino-acetic acid with aldehyde in presence of ethanol, acetic anhydride and sodium acetate. The structures of the new compounds were established on the basis of NMR and IR spectral data.
 Keywords
Substituted 4-Oxazol-5-One's;Antibacterial Activity;Synthesis;
 Language
English
 Cited by
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 References
1.
Lesieur; Aichaw, H. EUR PAT, 390, 673, 03 OCT1990; Chem Abstr, 1991, 114, 143.

2.
Ando, K.; Asai, N. EUR PAT, 385, 664, 05 SEPT 1990;Chem Abstr, 1991, 114, 143.

3.
Descas, P.; Jarry, C. EUR PAT, 392, 929, 17 OCT 1990;Chem Abstr, 1991,114, 143.

4.
Benedlt, D.; Daniel, V. J. Med. Chem. 1994, 37, 710. crossref(new window)

5.
Pereira, E. R.; Sancelme, M; Voldoire, A.; Prudhomme, M. Bio-org, Med-Chem. Lit. 1997, 7(190), 2503. crossref(new window)

6.
Viti, G.; Namnicine, R.; Ricci, R.; Pestelline, V.; Abeli, L.; Funo, M. Eur. J. Med. Chem. 1994, 29, 401. crossref(new window)

7.
Ahluwalia, V. K.; Das, U.; Sahaya, R. Indian Journal of Chemistry, 1999, 38B, 1129. crossref(new window)

8.
Balkrishana, K.; Prasantha, G.; David, B.; Isloor, A. M.Indian Journal of Hetrocyclic Chemistry 1999, 9, 47. crossref(new window)

9.
Desai, N. C.; Dave, D.; Shah, M. D.; Vyas, G. D. Indian Journal of Chemistry 2000, 348, 277. crossref(new window)

10.
Chuickshank, R.; Dugid, J. P.; Marmon, D. P.; Swain, R., H. A. In Medical microbiology, 1975; vol, 2 (Churchill-livingstone, Edinburgh, London).

11.
Indian Journal of Hetrocyclic Chemistry, 1999. vol.9. pp.47

12.
Indian Journal of Chemistry, 2000. vol.348. pp.277

13.
Chem. Abstr., 1991. vol.114. pp.143

14.
Chem. Abstr, 1991. vol.114. pp.14