Synthesis and antibacterial activity of isochromene and isoquinoline derivative

Journal of Heterocyclic Chemistry

Volumn 48, Issue 3, 2011, Pages 529-532

  Dabholkar, Vijay V ^a   Tripathi, Dilip R ^a  

^a KC College   (India)

Author keywords

[No Author keywords available]

Indexed keywords

2 IMINO 3 ( 1 OXO 3,4 DIPHENYL 1H ISOCHROMEN 6 YL) THIAZOLIDIN 5 ONE; 4 (2 IMINO 5 OXOTHIAZOLIDIN 3 YL) BENZOIC ACID; 4 THIOUREIDOBENZOIC ACID; 6 (2 IMINO 5 OXOTHIAZOLIDIN 3 YL) 3,4 DIPHENYL 2 (SUBSITUTED) ISOQUINOLIN 1(2H) ONE; ANILINE; ANTIINFECTIVE AGENT; BENZOIN; ISOCHROMENE; ISOQUINOLINE; POLYPHOSPHATE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ARTICLE; CORYNEBACTERIUM DIPHTHERIAE; DRUG STRUCTURE; DRUG SYNTHESIS; ESCHERICHIA COLI; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; INFRARED SPECTROPHOTOMETRY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; PSEUDOMONAS AERUGINOSA; STAPHYLOCOCCUS AUREUS; SUBSTITUTION REACTION;

EID: 79957477803     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.245     Document Type: Article

References (18)

1. Willis, I.; Kligman, A. M., Arch Dermatol 1970, 102, 405.
2. Sieve, B. F., South Med Surg 1942, 104, 135.
3. Wiesel, L. L.; Barritt, A. S.; Stumpe, W. M., Am J Med Sci 1951, 222, 243.
4. Hoshino, K.; Ishida, H.; Omovskaya, O.; Dudley, M.; Rleger, R.; Watkins, W. J.; Zhang, J. Z.; Renau, T. E.; Lee, V. J.; Ota, T.; Nakayama, K.; Ishida, Y.; Otsuka, M.; Kawato, H., Japan Kokai Tokkyo Koho, CODEN: JKXXAF JP 2002322054 A2 20021108: Japan, 2002
5. Hoshino, K.; Ishida, H.; Omovskaya, O.; Dudley, M.; Rleger, R.; Watkins, W. J.; Zhang, J. Z.; Renau, T. E.; Lee, V. J.; Ota, T.; Nakayama, K.; Ishida, Y.; Otsuka, M.; Kawato, H., Chem Abstr 2002, 137, 346134.
6. Shimada, Y., Japan Kokai Tokkyo Koho, CODEN: JXXAF JP 02113070 A2 19900425: Japan, 1990
7. Shimada, Y., Chem Abstr 1990, 113, 99405.
8. Majumder, P. L.; Guha, S.; Sen, S., Phytochemistry 1999, 52, 1365.
9. Papadakis, D. P.; Salemink, C. A.; Alikaridis, F. J.; Kephalas, T. A., Tetrahedron 1983, 39, 2223.
10. Kim, J. P.; Kim, W. G.; Koshino, H.; Jung, J.; Yoo, I. D., Phytochemistry 1996, 43, 425.
11. Kobayashi, S.; Tokumoto, T., J Chem Soc Chem Commun 1984, 1043.
12. Heptner, W.; Schacht, U.; Biochem Pharmacol 1974, 23, 3413.
13. Dandzidge, P. A.; Kaiser, C.; Brenner, M.; Gaitanopoulos, D.; Davis, L. D.; Webb, R. L.; Foley, J. J.; Sarau, H. M., J Med Chem 1984, 27, 28.
14. Cruickshank, R.; Duguid, J. P.; Marmion, B. P., Medicinal Microbiology, 12th ed.; Churchill Livingstone: London, 1975; Vol. 11.
15. Arthington-Skaggs, B. A.; Motley, M.; Morrison, C. J., J Clin Microbiol 2000, 38, 2254.
16. Joshua, C. P., J Org Chem 1963, 28, 1293.
17. Singh, V. K.; Pandey, V. K., Indian J Chem Sect B 2006, 45, 2745.
18. Application of polyphosphoric acid (PPA) arises from the fact that it is a mild reagent, even though a strongly dehydrating agent. It does not usually bring about charring or polymerization, most probably because it is a poor proton source.