Efficient synthesis of some 3-substuited-1(2H)-isoquinolones

Pharmaceutical Chemistry Journal

Volumn 42, Issue 5, 2008, Pages 277-280

  Saeed, Aamer ^a   Ashraf, Zaman ^b  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

^b Riphah Institute of Pharmaceutical Sciences   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

3 (2 BROMOPHENYL)ISOQUINOLIN 1(2H) ONE; 3 (2 CHLORO 4 FLUOROPHENYL)ISOQUINOLIN 1(2H) ONE; 3 (2 CHLOROBENZYL)ISOQUINOLIN 1(2H) ONE; 3 (2 CHLOROPYRIDYL)ISOQUINOLIN 1(2H) ONE; 3 (2,4 DICHLOROPHENYL)ISOQUINOLIN 1(2H) ONE; 3 (3 FLUOROPHENYL)ISOQUINOLIN 1(2H) ONE; 3 (3 IODOPHENYL)ISOQUINOLIN 1(2H ) ONE; 3 (3 IODOPHENYL)ISOQUINOLIN 1(2H) ONE; 3 (3 NITROPHENYL)ISOQUINOLIN 1(2H) ONE; 3 (4 FLUOROPHENYL)ISOQUINOLIN 1(2H) ONE; 3 PENTADECYLISOQUINOLIN 1(2H) ONE; ISOCARBOSTYRIL DERIVATIVE; ISOCOUMARIN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; PHYSICAL CHEMISTRY; REACTION ANALYSIS;

EID: 55949096440     PISSN: 0091150X     EISSN: 15739031     Source Type: Journal    
DOI: 10.1007/s11094-008-0105-y     Document Type: Article

References (36)

1. C.-Y. Chen F.-R. Chang C.-M. Teng Y.-C. Wu 1999 J. Chin. Chem. Soc. 46 77
2. G. R. Pettit Y. Meng D. L. Herald 2003 Nat. Prod. 66 1065
3. D. Gonzalez T. Martinot T. Hudlicky 1999 Tetrahedron Lett. 40 3077
4. R. C. Thompson J. Kallmerten 1990 J. Org. Chem. 55 6076
5. M. Shamma and J. L. Moniot, Isoquinoline Alkaloids Research, 1972-1977, Plenum Press, New York/London (1978), p. 57.
6. A. A. Semenov, The Chemistry of Natural Compounds [in Russian], Nauka/Siberian Printing Company of the Russian Academy of Sciences, Novosibirsk (2000). M. Shamma and J. E. Foy, Tetrahedron Lett., 2249 (1975).
7. T. Okomoto Y. Torii Y. Isogai 1968 Chem. Pharm. Bull. 16 1860
8. M. J. Fisher B. P. Gunn S. Um J. A. Jakubowski 1997 Tetrahedron Lett. 38 5747
9. T. Matsui T. Sugiura H. Nakai 1992 J. Med. Chem. 35 3307 3319
10. S. W. Li M. G. Nair D. M. Edwards 1991 J. Med. Chem. 34 2746 2754
11. Q. Chao L. Deng H. Shih 1999 J. Med. Chem. 42 3860 3873
12. T. S. Sulkovski M. A. Wille 1969 Chem. Abstr. 71 112830
13. K. Kubo N. Ito I. Souzu 1979 Chem. Abstr. 90 168468
14. O. Senda O. Ohtani E. Katho 1981 Chem. Abstr. 95 132692
15. M. Hasegava K. Shirai K. Matsumoto 1994 Chem. Abstr. 121 912
16. S. Gabriel J. Colman 1900 Chem. Ber. 33 980
17. M. C. Delcey C. Huel E. Bisagni 1995 Heterocycles 41 1721
18. J. E. Semple R. M. Rydzewski G. Gardner 1996 J. Org. Chem. 61 7967
19. Y. Cheng H.-B. Tsai M.-S. Lin 1995 J. Heterocycl. Chem. 32 73
20. A. Sugimoto, H. Shinba-Tanaka, and M. Ishikava, Synthesis, 431 (1995).
21. J. Dusemund T. Hardt 1988 Arch. Pharm. 321 41
22. S. Yamaguchi Y. Uchiuzoh K. Sanada 1995 J. Heterocycl. Chem. 32 419
23. S. Ohta and S. Kimoto, Tetrahedron Lett., 2279 (1975).
24. M. Khaldi F. Chrétien Y. Chapleur 1995 Tetrahedron Lett. 36 3003
25. G. E. Keck S. F. McHardy J. A. Murry 1995 J. Am. Chem. Soc. 117 7289
26. T. Minami A. Nishimoto M. Hanaoka 1995 Tetrahedron Lett. 36 9505
27. R. Connors E. Tran T. Durst 1996 Can. J. Chem. 74 221
28. J. H. Van Duzer D. M. Roland 1993 Chem. Abstr. 119 8694
29. M.-S. Chern W.-R. Li 2004 Tetrahedron Lett. 45 8323 8326
30. M. W. Khan A. F. G. M. Reza 2005 Tetrahedron 61 11204 11210
31. E. P. Souza P. S. Fernandes 1990 Ind. J. Chem. 29B 961
32. S. Ferrer D. P. Naughton H. Parveen M. D. Threadgill 2002 J. Chem. Soc., Perkin Trans. 1 335
33. T. Sakamoto M. Annaka Y. Kondo H. Yamanaka 1986 Chem. Pharm. Bull. 34 2754
34. A. S. Dmitriev, V. T. Abaev, and A. V. Butin, Chem. Heterocycl. Comp., 41 (2005).
35. E. Napolitano 1997 Org. Prep. Proced. Int. 29 631
36. A. Saeed 2003 Helvetica Chimica Acta 86 2 377 383