Sodium bromide catalysed one-pot synthesis of tetrahydrobenzo[b]pyrans via a three-component cyclocondensation under microwave irradiation and solvent free conditions

Tetrahedron Letters

Volumn 45, Issue 47, 2004, Pages 8625-8627

  Devi, Ipsita ^a   Bhuyan, Pulak J ^a  

^a REGIONAL RESEARCH LABORATORY   (India)

Author keywords

Microwave assisted reactions; Multicomponent reactions; Sodium bromide; Solvent free reactions; Tetrahydrobenzo b pyrans

Indexed keywords

SODIUM BROMIDE; SOLVENT; TETRAHYDROBENZO[B]PYRAN; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; DRUG SYNTHESIS; IRRADIATION; MICROWAVE RADIATION; POLYMERIZATION;

EID: 7044237277     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.09.158     Document Type: Article

References (35)

1. T. Tanaka, and F. Toda Chem. Rev. 100 2000 1025
2. L. Weber, K. Illegen, and M. Almstetter Synlett 1999 366
3. R.W. Armstrong, A.P. Combs, P.A. Tempest, S.D. Brown, and T.A. Keating Acc. Chem. Rev. 29 1996 123
4. A. Strecker Liebigs Ann. Chem. 75 1850 27
5. A.M. Shestopalov, Y.M. Emeliyanova, A.A. Shestiopolov, L.A. Rodinovskaya, Z.I. Niazimbetova, and D.H. Evans Org. Lett. 2002 423
6. B. List, and C. Castello Synlett 2001 1687
7. V. Nair, A.U. Vinod, and C. Rajesh J. Org. Chem. 66 2001 4427
8. M.C. Bagley, J.W. Cale, and J. Bower Chem. Commun. 2002 1682
9. J.F. Cheng, M. Chen, T. Arthenius, and A. Nadzen Tetrahedron Lett. 43 2002 6293
10. H.Z.S. Huma, R. Halder, S.S. Kalra, J. Das, and J. Iqbal Tetrahedron Lett. 43 2002 6485
11. F. Bertozzi, M. Gustafsson, and R. Olsson Org. Lett. 4 2002 3147
12. Y. Yuan, X. Li, and K. Ding Org. Lett. 4 2002 3309
13. U. Bora, A. Saikia, and R.C. Boruah Org. Lett. 5 2003 435
14. D. Dallinger, N.Y. Gorobets, and C.O. Kappe Org. Lett. 5 2003 1205
15. M. Pourashraf, P. Delair, M.O. Rasmaissen, and A.E. Greene J. Org. Chem. 65 2000 6966
16. J. Cossy, C. Willis, V. Bellosta, and L.S. Jalmes Synthesis 2002 951
17. G.R. Green, J.M. Evans, and A.K. Vong A.R. Katritzky C.W. Rees E.F.V. Scriven Comprehensive Heterocyclic Chemistry II Vol. 5 1995 Pergamon Press Oxford 469
18. W.O. Foye Prinicipi di Chemico Farmaceutica 1991 Piccin Padova, Italy p. 416
19. L.L. Andreani, and E. Lapi Bull. Chim. Farm. 99 1960 583
20. Y.L. Zhang, B.Z. Chen, K.Q. Zheng, M.L. Xu, and X.H. Lei Yao. Xue. Xue. Bao. 17 1982 17
21. Chem. Abstr. 96 1982 135383e
22. L. Bonsignore, G. Loy, D. Secci, and A. Calignano Eur. J. Med. Chem. 28 1993 517
23. E.C. Witte, P. Neubert, and A. Roesch Ger. Offen. DE 1986
24. Chem. Abstr. 104 1986 224915f
25. S. Hatakeyama, N. Ochi, H. Numata, and S. Takano J. Chem. Soc., Chem. Commun. 1988 1202
26. R. Gonzalez, N. Martin, C. Seoane, and J. Soto J. Chem. Soc., Perkin Trans. 1 1985 1202
27. D. Arnetso, W.M. Horspool, N. Martin, A. Ramos, and C. Seaone J. Org. Chem. 54 1989 3069
28. K. Singh, J. Singh, and H. Singh Tetrahedron 52 1996 14273
29. X.S. Wang, D.Q. Shi, S.J. Tu, and C.S. Yao Synth. Commun. 33 2003 119
30. G. Kaupp, M.R. Naimi-Zamal, and J. Schmeyers Tetrahedron 59 2003 3753
31. I. Devi, and P.J. Bhuyan Synlett 2004 283
32. I. Devi, H.N. Borah, and P.J. Bhuyan Tetrahedron Lett. 45 2004 2405
33. -1
34. Sharanina, L. G.; Nesterov, V. N.; Klokol, G. V.; Rodinovovskaya, L. A.; Shklover, V. E. J. Org. Chem. USSR (Engl. Transl.) 1986, 22, 1185, Zh. Org. Khim. 1986, 22, 1315
35. Sharanina, L. G.; Nesterov, V. N.; Klokol, G. V.; Rodinovovskaya, L. A.; Shklover, V. E. J. Org. Chem. USSR (Engl. Transl.) 1986, 22, 1185, Zh. Org. Khim. 1986, 22, 1315