Rapid synthesis of 1-amidoalkyl-2-naphthols over sulfonic acid functionalized imidazolium salts

Applied Catalysis A: General

Volumn 400, Issue 1-2, 2011, Pages 70-81

  Zolfigol, Mohammad Ali ^a   Khazaei, Ardeshir ^a   Moosavi Zare, Ahmad Reza ^a   Zare, Abdolkarim ^b   Khakyzadeh, Vahid ^a  

^a BU ALI SINA UNIVERSITY   (Iran)

^b PAYAME NOOR UNIVERSITY   (Iran)

Author keywords

Naphthol; 1 Amidoalkyl 2 naphthol; Ionic liquid; Solvent free; Sulfonic acid functionalized imidazolium salts

Indexed keywords

1-AMIDOALKYL-2-NAPHTHOL; AROMATIC ALDEHYDE; IMIDAZOLIUM; IMIDAZOLIUM SALT; MULTICOMPONENT CONDENSATION; ONE POT; RAPID SYNTHESIS; SHORT REACTION TIME; SOLVENT FREE; SOLVENT FREE CONDITIONS; SULFONIC ACID-FUNCTIONALIZED;

ALDEHYDES; AMIDES; CHLORINE COMPOUNDS; IONS; PHENOLS; SALTS; SYNTHESIS (CHEMICAL);

IONIC LIQUIDS;

EID: 79958176359     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2011.04.013     Document Type: Article

References (43)

1. R.D. Rogers, and K.R. Seddon Ionic Liquids: Industrial Applications to Green Chemistry 2002 American Chemical Society Washington, DC
2. V.I. Parvulescu, and C. Hardacre Chem. Rev. 107 2007 2615 2665
3. M.J. Earle, S.P. Katdare, and K.R. Seddon Org. Lett. 6 2004 707 710
4. B.C. Ranu, and S. Banerjee J. Org. Chem. 70 2005 4517 4519
5. B.C. Ranu, L. Adak, and S. Banerjee Can. J. Chem. 85 2007 366 371
6. D. Saha, A. Saha, and B.C. Ranu Tetrahedron Lett. 50 2009 6088 6091
7. A. Zare, A.R. Moosavi-Zare, A. Hasaninejad, A. Parhami, A. Khalafi-Nezhad, and M.H. Beyzavi Synth. Commun. 39 2009 3156 3165
8. A. Zare, A. Parhami, A.R. Moosavi-Zare, A. Hasaninejad, A. Khalafi-Nezhad, and M.H. Beyzavi Can. J. Chem. 87 2009 416 421
9. A. Hasaninejad, A. Zare, M. Shekouhy, and J. Ameri Rad J. Comb. Chem. 12 2010 844 849
10. M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare, and A. Zare J. Iran. Chem. Soc. 7 2010 646 651
11. M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare, and A. Zare Org. Prep. Proced. Int. 42 2010 95 102
12. A. Khazaei, M.A. Zolfigol, A.R. Moosavi-Zare, and A. Zare Sci. Iran.: Trans. C: Chem. Chem. Eng. 17 2010 31 36
13. C.-X. Miao, L.-N. He, J.-Q. Wang, and J.-L. Wang Adv. Synth. Catal. 351 2009 2209 2216
14. A.C. Cole, J.L. Jensen, I. Ntai, K.L.T. Tran, K.J. Weaver, D.C. Forbes, and J.H. Davis Jr. J. Am. Chem. Soc. 124 2002 5962 5963
15. T. Dingermann, D. Steinhilber, and G. Folkers Molecular Biology in Medicinal Chemistry 2004 Wiley-VCH Weinheim
16. A.Y. Shen, C.T. Tsai, and C.L. Chen Eur. J. Med. Chem. 34 1999 877 882
17. A.Y. Shen, C.L. Chen, and C.I. Lin Chin. J. Physiol. 35 1992 45 54
18. M. Damodiran, N.P. Selvam, and P.T. Perumal Tetrahedron Lett. 50 2009 5474 5478
19. Y. Kusakabe, J. Nagatsu, M. Shibuya, O. Kawaguchi, C. Hirose, and S. Shirato J. Antibiot. 25 1972 44 47
20. S. Remillard, L.I. Rebhun, G.A. Howie, and S.M. Kupchan Science 189 1975 1002 1005
21. G.Y. Lesher, and A.R. Surrey J. Am. Chem. Soc. 77 1955 636 641
22. H.S. Mosher, M.B. Frankel, and M. Gregory J. Am. Chem. Soc. 75 1953 5326 5328
23. J.L. Peglion, J. Vian, B. Gourment, N. Despaux, V. Audinot, and M. Millan Bioorg. Med. Chem. Lett. 7 1997 881 886
24. H. Ren, S. Grady, D. Gamenara, H. Heinzen, P. Moyna, S. Croft, H. Kendrick, V. Yardley, and G. Moyna Bioorg. Med. Chem. Lett. 11 2001 1851 1854
25. F. Benedini, G. Bertolini, R. Cereda, G. Doná, G. Gromo, S. Levi, J. Mizrahi, and A. Sala J. Med. Chem. 38 1995 130 136
26. R.D. Clark, J.M. Caroon, A.F. Kluge, D.B. Repke, A.P. Roszkowski, A.M. Strosberg, S. Baker, S.M. Bitter, and M.D. Okada J. Med. Chem. 26 1983 657 661
27. H. Matsuoka, N. Ohi, M. Mihara, H. Suzuki, K. Miyamoto, N. Maruyama, K. Tsuji, N. Kato, T. Akimoto, Y. Takeda, K. Yano, and T. Kuroki J. Med. Chem. 40 1997 105 111
28. N.P. Selvam, and P.T. Perumal Tetrahedron Lett. 47 2006 7481 7483
29. M.M. Khodaei, A.R. Khosropour, and H. Moghanian Synlett 2006 916 920
30. B. Das, K. Laxminarayana, B. Ravikanth, and B.R. Rao J. Mol. Catal. A: Chem. 261 2007 180 183
31. S.B. Patil, P.R. Singh, M.P. Surpur, and S.D. Samant Synth. Commun. 37 2007 1659 1664
32. H.R. Shaterian, H. Yarahmadi, and M. Ghashang Bioorg. Med. Chem. Lett. 18 2008 788 792
33. S.B. Patil, P.R. Singh, M.P. Surpur, and S.D. Samant Ultrason. Sonochem. 14 2007 515 518
34. H.R. Shaterian, H. Yarahmadi, and M. Ghashang Tetrahedron 64 2008 1263 1269
35. G.H. Mahdavinia, and M.A. Bigdeli Chin. Chem. Lett. 20 2009 383 386
36. A. Khazaei, M.A. Zolfigol, A.R. Moosavi-Zare, A. Zare, A. Parhami, and A. Khalafi-Nezhad Appl. Catal. A: Gen. 386 2010 179 187
37. A. Dorehgiraee, H. Khabazzade, and K. Saidi ARKIVOC vii 2009 303 310
38. G.C. Nandi, S. Samai, R. Kumar, and M.S. Singh Tetrahedron Lett. 50 2009 7220 7222
39. D. Kundu, A. Majee, and A. Hajra Catal. Commun. 11 2010 1157 1159
40. A.R. Hajipour, Y. Ghayeb, N. Sheikhan, and A.E. Ruoho Tetrahedron Lett. 50 2009 5649 5651
41. S.B. Sapkal, K.F. Shelke, B.R. Madje, B.B. Shingate, and M.S. Shingare Bull. Korean Chem. Soc. 30 2009 2887 2889
42. H. Khabazzadeh, K. Saidi, and N. Seyedi J. Chem. Sci. 121 2009 429 433
43. G. Srihari, M. Nagaraju, and M.M. Murthy Helv. Chim. Acta 90 2007 1497 1504