Highly efficient synthesis of 3-pyrrolyl-indolinones and pyrrolyl-indeno[1,2-b]quinoxalines catalyzed by heteropolyacids

Tetrahedron Letters

Volumn 49, Issue 37, 2008, Pages 5393-5396

  Karimi, Ali Reza ^a   Behzadi, Flora ^a   Amini, Mostafa Mohammadpour ^b  

^a ARAK UNIVERSITY   (Iran)

^b SHAHID BEHESHTI UNIVERSITY   (Iran)

Author keywords

4 Hydroxyproline; Heteropolyacid; Pyrroles

Indexed keywords

11H INDENOL[1,2 B]QUINOXALIN 11 ONE DERIVATIVE; 3 PYRROLYL INDOLINONE DERIVATIVE; ACETONITRILE; ALCOHOL; DIMETHYL SULFOXIDE; HETEROPOLYACID DERIVATIVE; HYDROXYPROLINE; INDOLE DERIVATIVE; ISATIN DERIVATIVE; PYRROLYL INDENO[1,2 B]QUINOXALINE DERIVATIVE; QUINOXALINE; SOLVENT; TUNGSTEN;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; POLYMERIZATION; ROOM TEMPERATURE; SYNTHESIS;

EID: 48149114486     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.07.015     Document Type: Article

References (29)

1. Ragno R., Marshall G.R., Di Santo R., Costi R., Massa S., Rompei R., and Artico M. Bioorg. Med. Chem. 8 (2000) 1423
2. Franc C., Denone F., Cuisiner C., and Ghosez L. Tetrahedron Lett. 40 (1999) 4555
3. Liu J., Yang Q., Mak T.C., and Wong H.N.C. J. Org. Chem. 65 (2000) 3587
4. Dieter R.K., and Yu H. Org. Lett. 2 (2000) 2283
5. Jefford C.W., Sienkiewicz K., and Thornton S.R. Helv. Chim. Acta 78 (1995) 1511
6. Amos R.I.J., Gourlay B.S., Molesworth P.P., Smith J.A., and Sprod O.R. Tetrahedron 61 (2005) 8226
7. Di Santo R., Costi R., Artico M., Massa S., Lampis G., Deidda D., and Rompei R. Bioorg. Med. Chem. Lett. 8 (1998) 2931
8. De Leon C.Y., and Ganem B. Tetrahedron 53 (1997) 7731
9. Thompson R.B. FASEB J. 15 (2001) 1671
10. Cozzi P., and Mongelli N. Curr. Pharm. Des. 4 (1998) 181
11. Furstner A., Szillat H., Gabor B., and Mynott R. J. Am. Chem. Soc. 120 (1998) 8305
12. Muchowski J.M. Adv. Med. Chem. 1 (1992) 109
13. Lainton J.A.H., Hoffman J.W., Martin B.R., and Compton D.R. Tetrahedron Lett. 36 (1995) 1401
14. Jones R.A., and Bean G.P. The Chemistry of Pyrroles (1977), Academic Press, London pp 1-5
15. Gilchrist T.L. J. Chem. Soc., Perkin. Trans. 1 (1998) 615
16. Yu S.-X., and Le Quesne P.W. Tetrahedron Lett. 36 (1995) 6205
17. Paal C. Chem. Ber. 17 (1884) 2756
18. Knorr L. Chem. Ber. 17 (1884) 2863
19. Azizian J., Karimi A.R., Kazemizadeh Z., Mohammadi A.A., and Mohammadizadeh M.R. J. Org. Chem. 70 (2005) 1471
20. Azizian J., Karimi A.R., Kazemizadeh Z., Mohammadi A.A., and Mohammadizadeh M.R. Tetrahedron Lett. 46 (2005) 6155
21. Azizian J., Karimi A.R., Kazemizadeh Z., Mohammadi A.A., and Mohammadizadeh M.R. Synthesis (2005) 1095
22. Yadav J.S., Subba Reddy B.V., Jain R., and Suresh Reddy Ch. Tetrahedron Lett. 48 (2007) 3295
23. Yadav J.S., Subba Reddy B.V., Jain R., and Subba Reddy U.V. J. Mol. Catal. A: Chem. 278 (2007) 38
24. Banik B.K., and Cardona M. Tetrahedron Lett. 47 (2006) 7385
25. Kozhhevnikov I.V. Chem. Rev. 98 (1998) 171
26. Kozhhevnikov I.V. In: Derouane E. (Ed). Catalysis for Fine Chemical Synthesis, Catalysis by Polyoxometalates 2 (2002), Wiley, New York
27. Romanelli G.P., Bennardi D., Ruiz D.M., Baronetti G., Thomas H.J., and Autino J.C. Tetrahedron Lett. 45 (2004) 8935
28. Amini M.M., and Shaabani A. Catal. Commun. 7 (2006) 843
29. pyrrole), 115.84, 120.41, 127.16, 128.44, 133.18, 140.29 (arom), 173.98 (C{double bond, long}O).