1-Hexanesulphonic acid sodium salt promoted the one-pot synthesis of amidoalkyl naphthols under microwave-irradiation

Chinese Chemical Letters

Volumn 22, Issue 5, 2011, Pages 551-554

  Niralwad, Kirti S ^a   Shingate, Bapurao B ^a   Shingare, Murlidhar S ^a  

^a DR BABASAHEB AMBEDKAR MARATHWADA UNIVERSITY   (India)

Author keywords

1 Hexanesulphonic acid sodium salt; Aldehydes; Amidoalkyl naphthols; Microwave irradiation; Naphthols

Indexed keywords

EID: 79952986589     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2010.11.018     Document Type: Article

References (37)

1. R. Gedye, F. Smith, and K. Westaway Tetrahedron Lett. 27 1986 279
2. A. Loupy Microwave in Organic Synthesis 2006 Wiley-VCH Weinheim
3. R.J. Giguere, T.L. Bray, S.M. Duncan, and G. Majetich Tetrahedron Lett. 27 1986 4945
4. D.R. Hwang, S.M. Moerlein, and M.J. Welch J. Chem. Soc., Chem. Commun. 23 1987 1799
5. A. Gourdenne, and Q. Le Van Polym. Prep. 22 1981 125
6. H. Jullien, and H. Valot Polymer 24 1983 810
7. A. Loupy, S.J. Song, and S.J. Cho Synth. Commun. 35 2005 79
8. A. Loupy, A. Haudrechy, Effect de Milieu en Synthese Organique, Masson, Paris, 1996.
9. D.A. Lewis, J.D. Summers, and T.C. Ward J. Polym. Sci. Part A 30 1992 1647
10. J. Berlan, P. Giboreau, and S. Lefeuvre Tetrahedron Lett. 32 1991 2363
11. C.R. Strauss, and R.S. Varma Top. Curr. Chem. 266 2006 199
12. I. Ugi, A. Domling, and W. Horl Endeavour 18 1994 115
13. L.F. Tietze, and A. Modi Med. Res. Rev. 20 2000 304
14. I. Ugi, A. Domling, and B. Werner J. Heterocycl. Chem. 37 2000 647
15. R.V.A. Orru, and M. de Greef Synthesis 2003 1471
16. E. Juaristi, Enantioselective Synthesis of Amino-acids, John Wiley & Sons, New York, 1997.
17. T. Dingermann, D. Steinhilber, G. Folkers, Wiley-VCH, Weinheim, 2004.
18. S. Kantevari, S.V.N. Vuppalapati, and L. Nagarapu Catal. Commun. 8 2007 1857
19. N.P. Selvam, and P.T. Perumal Tetrahedron Lett. 47 2006 7481
20. B. Das, K. Laxminarayana, and B. Ravikanth J. Mol. Catal. A: Chem. 261 2007 180
21. L. Nagarapu, M. Baseeruddin, and S. Apuri Catal. Commun. 8 2007 1729
22. M.M. Khodaei, A.R. Khosropour, and H.A. Moghanian Synlett 6 2006 916
23. S.B. Patil, P.R. Singh, M.P. Surpur, and S.D. Samant Ultrason. Sonochem. 14 2007 515
24. S.B. Patil, P.R. Singh, M.P. Surpur, and S.D. Samant Synth. Commun. 37 2007 1659
25. G. Srihari, M. Nagaraju, and M.M. Murthy Helv. Chim. Acta 90 2007 1497
26. H.R. Shaterian, H. Yarahmadi, and M. Ghashang Tetrahedron 64 2008 1263
27. H.R. Shaterian, and H. Yarahmadi Arkivoc 2 2008 105
28. J. Weiss V.C.H. Verlags gesellschaft mbH IInd ed. 1995 VCH Publisher, Inc. New York, Weinheim, Germany
29. H. Small Ion Chromatography 1989 Plenum Press New York and London
30. J.L. Boyer, B. Gilot, and J.P. Canselierm Phosphorus Sulphur Silicon Relat. Elem. 20 1984 259
31. R.S. Joshi, P.G. Mandhane, S.D. Diwakar, and C.H. Gill Ultrason. Sonochem. 17 2010 298
32. K.S. Niralwad, B.B. Shingate, and M.S. Shingare Ultrason. Sonochem. 17 2010 760
33. K.S. Niralwad, B.B. Shingate, and M.S. Shingare Bull. Korean Chem. Soc. 31 2010 981
34. S.B. Sapkal, K.F. Shelke, B.B. Shingate, and M.S. Shingare Tetrahedron Lett. 50 2009 1754
35. K.S. Niralwad, B.B. Shingate, and M.S. Shingare Tetrahedron Lett. 51 2010 3616
36. S.A. Sadaphal, K.F. Shelke, S.S. Sonar, and M.S. Shingare Central Eur. J. Chem. 6 2008 622
37. 2: C 68.83, H 6.60, N 11.47; found C 69.11, H 6.62, N 11.54.