A convenient synthesis of some coumarin derivatives using SnCl2 • 2H2O as catalyst

Catalysis Letters

Volumn 121, Issue 1-2, 2008, Pages 118-120

  Upadhyay, K K ^a   Mishra, Rakesh K ^a   Kumar, Ajit ^a  

^a BANARAS HINDU UNIVERSITY   (India)

Author keywords

2H2O; Coumarin; SnCl2; Von Pechmann condensation

Indexed keywords

CATALYST ACTIVITY; CONDENSATION; ETHANOL; SYNTHESIS (CHEMICAL); TIN COMPOUNDS;

COUMARIN DERIVATIVES; ETHANOLIC MEDIUM;

DERIVATIVES;

EID: 38349089875     PISSN: 1011372X     EISSN: 1572879X     Source Type: Journal    
DOI: 10.1007/s10562-007-9307-2     Document Type: Article

References (41)

1. Murray RDH (1991) Prog Chem Org Nat Prod 58:84-316
2. Lin CM, Huang ST, Lee FW, Sawkuo H, Lin MH (2006) Bioorg Med Chem 14:4402
3. Bhat MA, Siddiqui N, Khan SA (2006) Indian J Pharm Sci 68:120
4. Massimo C, Francesco E, Federica M, Carla MM, Prieto GS, Carlos RJ (2003) Aust J Chem 56:59
5. Ruszat R, Wyler S, Forster T, Reich O, Christian GS, Thomas CG, Sulser T, Bachmann A (2006) Eur Assoc Urol (In press)
6. Tyagi AK, Raj HG, Vohra P, Gupta G, Kumari R, Kumar P, Gupta RK (2003) Eur J Med Chem 40:413
7. Modrana JN, Nawrot E, Graczyk J (2006) Eur J Med Chem 41:1301
8. Sardari S, Mori Y, Horita K, Micetich RG, Nishibe S, Daneshtalab M (1999) Bioorg Med Chem 7:1933
9. Huang L, Yuon X, Yu D, Lee KH, Chin HC (2005) Virology 332:623
10. Elinos-Baez CM, Leon F, Santos E (2005) Cell Biol int 29:703
11. Mohanty N, Rath PC, Rout MK (1967) J Indian Chem Soc 44:1001
12. Kennedy RO, Tharnes RD (1997) Coumarins: biology, application and mode of action. Wiley & Sons, Chichester
13. Zahradnik M (1992) The production and application of fluorescent brightening Agents. Wiley & Sons
14. Maeda M (1994) Laser dyes. Academic, New York
15. Ghosh K, Adhikari S (2006) Tetrahedron Lett 47:8165
16. von Pechmann H, Duisberg C (1884) Chem Ber 17:929
17. Jonson JR (1942) Org React 1:210
18. Jones G (1967) Org React 15:204
19. Brufola G, Fringuelli F, Piermatti O, Pizzo F (1996) Heterocycles 43:1257
20. Shriner RL (1942) Org React 1:1
21. Narasimahan NS, Mali RS, Barve MV (1979) Synthesis. 906
22. Yavari I, Hekmat-Shoar R, Zonouzi A (1998) Tetrahedron Lett 39:2391
23. Raschig F (1909) Ger Pat 223:684
24. Potdar MK, Mohile SS, Salunkhe MM (2001) Tetrahedron Lett 42:9285
25. Chavan SP, Shivasankar K, Sivappa R, Kale R (2002) Tetrahedron Lett 43:8583
26. Valizadeh H, Shockravi A (2005) Tetrahedron Lett 46:3501
27. Sharma GVM, Reddy JJ, Lakshmi PS, Krishna PR (2005) Tetrahedron Lett 46:6119
28. Bose DS, Rudradas AP, Babu MH (2002) Tetrahedron Lett 43:9195
29. Sun P, Hu Z (2005) Synth Commun 35:1875
30. Bahekara SS, Shindeb DB (2004) Tetrahedron Lett 45:7999
31. Alexander VM, Bhat RP, Samant SD (2005) Tetrahedron Lett 46:6957
32. Heravi MM, Khorasani M, Derikvand F, Oskooie HA, Bamoharram FF (2007) Catalysis Communications (Accepted)
33. Hegedus A, Hell Z (2006) Catalysis Lett 112:105
34. Selvakumar S, Chidambaram M, Singh AP (2007) Catal Commun 8:777
35. Russowsky D, Lopes FA, da Silva VSS, Canto KFS, Montes D'Oca MG, Godoi MN (2004) J Braz Chem Soc 15:165
36. Madapa S, Singh V, Batra S (2006) Tetrahedron 62:8740
37. Kumar S, Saini A, Sandhu JS (2004) Indian J Chem 43B:1485
38. Kumar S, Saini A, Sandhu JS (2005) Indian J Chem 44B:762
39. Mishra L, Upadhyay KK (1994) Indian J Chem 33A:683
40. Upadhyay KK, Kumar A, Upadhyay S, Mishra PC (2007) J Mol Struct (In Press)
41. Wilson SC, Howard PW, Thurston DE (1995) Tetrahedron lett 36:6333