Heterocyclic synthesis: A convenient route to some 2-mercepto 1,3,4-oxadiazole and green chemistry microwave-induced one-pot synthesis of 2-aryl 1,3,4-oxadiazole in quinazolone and their antibacterial and antifungal activity

Journal of Heterocyclic Chemistry

Volumn 42, Issue 5, 2005, Pages 995-999

  Desai, A R ^a   Desai, K R ^a  

^a VEER NARMAD SOUTH GUJARAT UNIVERSITY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

1,3,4 OXADIAZOLE DERIVATIVE; 2 [6 BROMO 2 METHYL 4 OXOQUINAZOLIN 3(4H) YL]BENZOHYDRAZIDE; 2 [6 BROMO 2 PHENYL 4 OXOQUINAZOLIN 3(4H) YL]ACETOHYDRAZIDE; 6 BROMO 2 METHYL 3 [4 (5 PHENYL 1,3,4 OXADIAZOL 2 YL)PHENYL]QUINAZOLIN 4(3H) ONE; 6 BROMO 3 [4 (5 MERCAPTO 1,3,4 OXADIAZOL 2 YL)PHENYL] 2 METHYLQUINAZOLIN 4(3H) ONE; AMOXICILLIN; AMPICILLIN; BENZOIC ACID; FLUCONAZOLE; PENICILLIN G; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ARTICLE; CANDIDA; CANDIDA KRUSEI; DRUG SYNTHESIS; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; MICROWAVE RADIATION;

EID: 22244470358     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570420539     Document Type: Article

References (22)

1. W. Xie, Y. Jin and P. G. Wang, Chemtech., 29, 23 (1999).
2. R. S. Verma, Green Chem., 1, 43 (1999).
3. M. Kidwai, Pure Appl. Chem., 73, 147 (2001).
4. H. L. Yale and K. Losee, J. Med. Chem., 9, 478 (1966).
5. D. Ghiran, I. Schwartz and I. Simiti, Farmacia., 22, 141 (1974).
6. J. Thomas, German Patent 2403357 (1974);
7. Chem. Abstr., 81, 136153 (1974).
8. G. W. Adelstein, C. H. Yen, E. Z. Dajani and R. G. Bianchi, J. Med. Chem. 19, 1221 (1976).
9. E. Schinzel, T. Martini, W. Spatzeier, H. Probst and A. G. Hoechst and De. Patent 3126464 (1983/1981);
10. Chem Abstr., 98, 199850 (1983).
11. N. K. Chudhgar, S. N. Shah and R. A. Vora, Mol. Cryst. Liq. Cryst., 51, 172 (1989).
12. Y. Gan, D. Lu, J. Liu and M. Tian, Zhongguo Yaouri Zazhi, 11, 85 (2001);
13. Chem Abstr., 136, 216696 (2002).
14. G. Turan-Zitouni, M. Sivaci, F. S. Kilic and K. Erol, Eur. J. Med. Chem., 36, 685 (2002).
15. S. Sharma, V. K. Srivastava and A. Kumar, Eur. J. Med. Chem., 37, 689 (2002).
16. J. C. Jung, E. B. Watkins and M. A. Avery, Tetrahedron., 58, 3696 (2002)
17. V. K. Ahluwalia and S. Dudeja, Synth. Commun., 31, 3175 (2001).
18. [15a] R. S. Sharma and S. C. Bahel, J. Ind. Chem. Soc., 59, 877 (1982);
19. [b] S. A. Shiba, A. A. El-Khamry, M. E. Shaban and K. S. Atia, Indian J. Chem., 36B, 361 (1997).
20. J. C. Jung, E. B. Watkins and M. A. Avery, Synth. Commun., 32, 3767 (2002).
21. [17a] M. Kidwai, S. Saxena, R. Mohan and R. Venkataramanan, J. Chem. Soc., Perkin Trans 1. 16, 1845 (2002);
22. [b] M. Kidwai, S. Rastogi and R. Venkataramanan, Bull. Chem. Soc. Jpn., 76, 203 (2003).