Synthesis of new isoxazolyl coumarins by eco-friendly dipyridine cobalt chloride catalyzed Pechmann reaction at ambient temperature

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry

Volumn 49, Issue 4, 2010, Pages 532-535

  Rajanarendar, E ^a   Shaik, Firoz Pasha ^a   Reddy, M Nagi ^a  

^a KAKATIYA UNIVERSITY   (India)

Author keywords

ketoesters; Dipyridine cobalt chloride; Isoxazolyl coumarins; Isoxazolyl phenols

Indexed keywords

EID: 77956094004     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (36)

1. Singer L A & Kong N P, J Am Chem Soc, 88 (22), 1966, 5213.
2. Fan G J, Mar. W, Park M K, Wook Choi E, Kim K & Kim S, Bioorg Med Chem Lett, 11, 2001, 2361.
3. Kirkiacharian S, Thuy D T, Sic Sic S, Bakhchinian R, Kurkjian R & Tonaire T, Il Farmaco, 57, 2002, 703.
4. Murray R D H, Medez S A & Brown, The natural Coumarins: Occurrence, Chemistry and Biochemistry, (Wiley, New York), 1982.
5. Kennedy O & Thornes R D, Coumarins: Biology, Applications and mode of action (Wiley & Sons, Chichester), 1997.
6. Zahradnik M, The production and Application of Fluorescent Brightening Agents (Wiley & Sons, Chichester), 1992.
7. Maeda M, Laser dyes, (Academic Press, New York), 1984.
8. Eugster, Prog Chem Org Nat Prod, 27, 1969, 261.
9. Kano H, Adachi I, Kido R & Hirose K, J Med Chem, 10 (3), 1967, 411.
10. Reddy P B, Reddy S M, Rajanarendar E & Murthy A K, Indian Phytopathology, 37, 1984, 370.
11. Getal J, Antibiot, 28 (1), 1975, 91.
12. Sadanandam A, Rajam M V, Subash K & Rajanarendar E, J Indian Bot Report, 3 (1), 1984, 38.
13. John M, Ludwig S, Nicholas R N, Roger D W, Bruce E M & Stephen F F, J Med Chem, 31, 1988, 473.
14. Sethna S M & Phadke R, Org React, 7, 1953, 1.
15. (a) Jones G, Org React, 15, 1967, 204.
16. Shirner R L, Org React, 1, 1992, 1.
17. (a) Narasimhan N S, Mali R S & Barve M V, Synthesis, 1979, 906.
18. (a) Appel H, J Chem Soc, 1935, 1031;
19. (b) Woods L L & Sapp J, J Org Chem, 27, 1962, 3703;
20. (c) Ahmad Z S & Desai R D, Proc Indian Acad Sci, 5A, 1937, 277;
21. (d) Robinson R & Weygand F, J Chem Soc, 1941, 386.
22. Boswas G K, Basu K, Barna A K & Battacharya P, Indian J Chem, 31B, 1992, 628.
23. Subba Rao Y B, Kulkarni S J, Subramanyan M & Rama Rao A V, 7 Chem Soc, Chem Commun, 1993, 1456.
24. Hoefnagel A J, Gunnewegh E A, Downing R S & Van Bekkum H, J Chem Soc, Chem Commun, 1995, 225.
25. Dela Hoz A, Moreno A & Vaz quez E, Synlett, 1999, 608.
26. Subhas Bose D, Rudradas A P & Haribabu M, Tetrahedron Lett, 43, 2002, 9195.
27. Smitha G & Sanjeeva Reddy Ch, Synth Commun, 34, 2004, 3997.
28. Wang L, Xia J, Tian H, Qian C & Ma Y, Indian J Chem, 42B, 2003, 2097.
29. Sugino T & Tanaka K, Chemistry Lett, 4, 2001, 110.
30. Duntiz J D, Acta Cryst, 10, 1957, 307.
31. Madhav J V, Kuarm B S, Someshwar P, Rajitha B, Reddy Y R T & Crooks P A, J Chem Res, 4, 2008, 232.
32. (a) Rajanarendar E, Ramesh P & Ramu K, Indian J Chem, 43B, 2004, 2650;
33. (b) Rajanarendar E, Ramu K, Karunakar D & Ramesh P, J Heterocyclic Chem, 42, 2005, 711;
34. (c) Rajanarendar E, Ramesh P, Srinivas M, Ramu K & Mohan G, Synth Commun, 36, 2006, 665;
35. (d) Rajanarendar E, Mohan G, Ramesh P & Karunakar D, Tetrahedron Lett, 47, 2006, 4957;
36. (e) Rajanarendar E, Ramesh P, Kalyan Rao E, Mohan G & Srinivas M, Arkivoc (xiv), 2007, 266.