A synthetic route to 11-(1H-pyrrol-1-yl)-11H-indeno[1,2-b]quinoxaline derivatives exploiting a three-component coupling strategy under microwave irradiation

Tetrahedron Letters

Volumn 46, Issue 36, 2005, Pages 6155-6157

  Azizian, Javad ^a   Karimi, Ali Reza ^a   Kazemizadeh, Zahra ^a   Mohammadi, Ali A ^a   Mohammadizadeh, Mohammad R ^a  

^a SHAHID BEHESHTI UNIVERSITY   (Iran)

Author keywords

Microwave irradiation; Pyrroles; Three component reaction

Indexed keywords

DIAMINE DERIVATIVE; HYDROXYPROLINE; MONTMORILLONITE; NINHYDRIN; QUINOXALINE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; MICROWAVE IRRADIATION; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 23244454493     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.06.099     Document Type: Article

References (19)

1. G.H. Posner Chem. Rev. 86 1986 831 844
2. A. Domling, and I. Ugi Angew. Chem., Int. Ed. 39 2000 3167 3210
3. I. Ugi, A. Domling, and B. Werner J. Heterocycl. Chem. 37 2000 647 658
4. H. Bienayme', C. Hulme, G. Oddon, and P. Schmitt Chem. Eur. J. 6 2000 3321 3329
5. I. Ugi, and S. Heck Comb. Chem. High Throughput Screen. 4 2001 1 34
6. V. Nair, C. Rajesh, A.U. Vinod, S. Bindu, A.R. Sreekanth, J.S. Mathen, and L. Balagopala Acc. Chem. Res. 36 2003 899 907
7. S. Kobayashi Chem. Soc. Rev. 28 1999 1 15
8. For a review on the synthesis of pyrroles, see: V.F. Ferreira, M.C.B.V. Souza, A.C. Cunha, L.O.R. Pereira, and M.L.G. Ferreira Org. Prep. Proced. Int. 33 2001 411 454
9. M. Adamczyk, and R.E. Reddy Tetrahedron Lett. 37 1996 2325 2326
10. R.U. Braun, and T.J.J. Muller Synthesis 2004 2391 2406
11. A. Arcadi, R. Anacardio, G. D'Anniball, and M. Gentile Synlett 11 1997 1315 1317
12. H. Tsutsuzi, M. Kitamura, and K. Narasaka Bull. Chem. Soc. Jpn. 74 2002 1451 1460
13. K.C. Joshi, R. Jain, and P. Chand Heterocycles 23 1985 957
14. J. Azizian, A.A. Mohammadi, A.R. Karimi, and M.R. Mohammadizadeh J. Org. Chem. 70 2005 350 352
15. J. Azizian, A.R. Karimi, and A.A. Mohammadi Synth. Commun. 33 2003 383 387
16. J. Azizian, A.R. Karimi, H. Arefrad, A.A. Mohammadi, and M.R. Mohammadizadeh Mol. Diversity 6 2003 223 226
17. J. Azizian, A.A. Mohammadi, and A.R. Karimi Synth. Commun. 33 2003 415 420
18. J. Azizian, A.R. Karimi, Z. Kazemizadeh, A.A. Mohammadi, and M.R. Mohammadizadeh J. Org. Chem. 70 2005 1471 1473
19. 3: C, 81.00; H, 5.50; N, 13.49. Found: C, 79.88; H, 5.55; N,13.51.