Synthesis and spectral characterization of novel 1,3,4-oxadiazole and 1,2,4-triazole derivatives: Synthesis for potential pharmacological activities

Phosphorus, Sulfur and Silicon and Related Elements

Volumn 177, Issue 1, 2002, Pages 67-79

  Faidallah, Hassan M ^a   Sharshira, Essam M ^a   Basaif, Salem A ^b   A Ba Oum, Abd El Kader ^b  

^a Alexandria University Faculty Of Science   (Egypt)

^b KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

Author keywords

1,2,4 triazole; 1,3,4 oxadiazole; Thiosemicarbazide

Indexed keywords

1,2,4 TRIAZOLE DERIVATIVE; 1,3,4 OXADIAZOLE DERIVATIVE; 2 4 CHLOROPHENYL 3 (4' ACETYL 5' PHENYL 4',5' DIHYDRO 1',3',4' OXADIAZOL 2' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 4 CHLOROPHENYL 3 (5' MERCAPTO 4' PHENYL 1',2',4' TRIAZOL 3' YL) 4,5 DIHYDRONAPHTHO[1,2 C[PYRAZOLE; 2 4 CHLOROPHENYL 3 (5' MERCAPTO 4' PHENYL 1',2',4' TRIAZOL 3' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 4 CHLOROPHENYL 3 (5' PHENYL 1',3',4' OXADIAZOL 2' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 4 CHLOROPHENYL 3 (5' PHENYLAMINO 1',3',4' OXADIAZOL 2' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 4 SULFAMYLPHENYL 3 (5' PHENYLAMINO 1',3',4' OXADIAZOL 2' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 PHENYL 3 (4' ACETYL 5' PHENYL 4',5' DIHYDRO 1',2',4' OXADIAZOL 2' TL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 PHENYL 3 (5' MERCAPTO 4' PHENYL 1',2',4 TRIAZOL 3' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 PHENYL 3 (5' PHENYL 1',3',4' OXADIAZOL 2' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; 2 PHENYL 3 (5' PHENYLAMINO 1',3',4' OXADIAZOL 2' YL) 4,5 DIHYDRONAPHTHO[1,2 C]PYRAZOLE; ACETIC ANHYDRIDE; BENZYLIDENE DERIVATIVE; MERCURIC OXIDE; SODIUM HYDROXIDE; THIOSEMICARBAZIDE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; DESULFURIZATION; DRUG SYNTHESIS; INFRARED RADIATION; MELTING POINT; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME;

EID: 0036035618     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/10426500210235     Document Type: Article

References (14)

1. M. I. H. Kittur and C. S. Mahajanshetti, J. Oil Technol. Assoc. India (Bombay), 18, 49 (1986).
2. C. S. Andotra and S. K. Sharma, Indian J. Pharm. Sci., 51, 107 (1989).
3. A. R. Katoitzky, H. M. Faidalloh, H. Aghabozorg, and G. J. Palenik, Chemica Scripta, 23, 134 1984).
4. P. W. West and J. Warkentin, J. Org. Chem., 33, 2089 (1968).
5. H. L. Yale, K. Losee, J. Martins, M. Holsing, F. M. Perry, and J. Bernstein, J. Am. Chem. Soc., 75, 1933 (1953).
6. M. M. El-Sadek, H. M. Faidallah, N. N. El-Soccary, and S. Y. Hassan, Egypt. J. Chem. 38, 435 (1995).
7. H. M. Faidallah, M. S. I. Makki, A. H. I. El-Massry, and S. Y. Hassan, Pharmazie, 52, 1010 (1997).
8. H. A. Albar, M. S. I. Makki, and H. M. Faidallah, Indian J. Chem., 35B, 23 (1996).
9. K. Mehta and H. Parekh, J. Indian Chom. Soc., 65, 521 (1988).
10. S. P. Suman and S. C. Babel, Agric. Biol. Chem., 43, 1339 (1979).
11. M. Yamamoto, S. Morooka, M. Koshiba, S. Inaba, and H. Yamamoto, Jpn. Kokai, 76/100, 098 (1976). [CA 86, 121364 (1977)].
12. R. Westwood, W. R. Tully, and R. Murdoch, Eur. Pat. 34, 529 (1981).
13. M. A. E. Shaban, M. A. M. Taha, and E. M. Sharshira, Advances in Heterocyclic Chemistry, 52, 1 (1991).
14. H. M. Faidallah, S. A. Basaif, E. M. Sharshira, and A. E. A-Ba-Oum, Unpublished results.