Cellulose-SO 3H as a biodegradable solid acid catalyzed one-pot three-component Ugi reaction: Synthesis of α-amino amide, 3,4-dihydroquinoxalin-2-amine, 4H-benzo[b][1,4]thiazin-2-amine and 1,6-dihydropyrazine-2,3-dicarbonitrile derivatives

Journal of Molecular Catalysis A: Chemical

Volumn 360, Issue , 2012, Pages 26-34

  Mofakham, Hamid ^a   Hezarkhani, Zeinab ^a   Shaabani, Ahmad ^a  

^a SHAHID BEHESHTI UNIVERSITY   (Iran)

Author keywords

Amino amide; Biodegradable solid acid catalyzed; Cellulose SO 3H; Solid acid catalyzed; Three compound Ugi reaction

Indexed keywords

CELLULOSE-SO 3H; ONE POT; ROOM TEMPERATURE; SOLID ACID; SOLID ACID CATALYSTS; THREE-COMPONENT; UGI REACTION;

AMIDES; CATALYSIS; CELLULOSE; ETHANOL; SULFURIC ACID;

ORGANIC COMPOUNDS;

EID: 84861636550     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2012.04.002     Document Type: Article

References (39)

1. R.A. Sheldon, and H. van Bekkum Fine Chemicals through Heterogeneous Catalysis 2001 Wiley-VCH Weinheim
2. S.K. De Synth. Commun. 35 2005 653
3. D. Klemm, B. Heublein, H.-P. Fink, and A. Bohn Angew. Chem. Int. Ed. 44 2005 3358
4. R. Breslow Acc. Chem. Res. 13 1980 170
5. J.H. Clark, and D.J. Macquarrie Green Chemistry and Technology 2002 Blackwell Abingdon
6. W.L. Wei, H.Y. Zhu, C.L. Zhao, M.Y. Huang, and Y.Y. Jiang React. Funct. Polym. 59 2004 33
7. C. Crecchio, P. Ruggiero, and M.D.R. Pizzigallo Biotechnol. Bioeng. 48 1995 585
8. H. Gliemann, U. Nickel, and S. Schneider J. Raman Spectrosc. 29 1998 89
9. K. Huang, L. Xue, Y.C. Hu, M.Y. Huang, and Y.Y. Jiang React. Funct. Polym. 50 2002 199
10. E. Guibal Prog. Polym. Sci. 30 2005 71
11. I. Ugi, C. SteinbrQckner, DE 1103337, 1959.
12. I. Ugi, and S. Cornelius Chem. Ber. 94 1961 734
13. J.W. McFarland J. Org. Chem. 28 1963 2179
14. N. Kreutzkamp, and K. Lammerhirt Angew. Chem. Int. Ed. Engl. 7 1968 372
15. Y. Tanaka, T. Hasui, and M. Suginome Org. Lett. 9 2007 4407
16. L.B. Mullen, and J.D. Sutherland Angew. Chem. Int. Ed. 46 2007 8063
17. S.C. Pan, and B. List Angew. Chem. Int. Ed. 47 2008 3622
18. A. Shaabani, A. Maleki, and J. Moghimi-Rad J. Org. Chem. 72 2007 6309
19. A. Shaabani, A. Maleki, H. Mofakham, and H.R. Khavasi J. Comb. Chem. 10 2008 323
20. A. Shaabani, A. Maleki, H. Mofakham, and J. Moghimi-Rad J. Org. Chem. 73 2008 3925
21. A. Shaabani, A. Maleki, and H. Mofakham J. Comb. Chem. 10 2008 595
22. A. Shaabani, A. Maleki, F. Hajishaabanha, H. Mofakham, M. Seyyedhamzeh, M. Mahyari, and S.W. Ng J. Comb. Chem. 12 2010 186
23. A. Shaabani, A.H. Rezayan, A. Rahmati, and M. Sharifi Monatsh. Chem. 137 2006 77
24. A. Shaabani, A. Rahmati, A.H. Rezayan, M. Darvishi, Z. Badri, and A. Sarvary QSAR Comb. Sci. 26 2007 973
25. A. Shaabani, A. Rahmati, and J. Moghimi Rad Comptes Rendus Chimie 11 2008 759
26. A. Shaabani, A.H. Rezayan, A. Sarvary, A. Rahmati, and H.R. Khavasi Catal. Commun. 9 2008 1082
27. A. Shaabani, and A. Maleki Appl. Catal. A: Gen. 331 2007 149
28. A. Shaabani, A. Rahmati, and Z. Badri Catal. Commun. 9 2008 13
29. A. Shaabani, A. Maleki, and J. Moghimi-Rad Chem. Pharm. Bull. 55 2007 957
30. M.A. Zolfigol Tetrahedron 57 2001 9509
31. A. Shaabani, A. Maleki, M.R. Soudi, and H. Mofakham Catal. Commun. 10 2009 945
32. M.M. Heravi, B. Baghernejad, and H.A. Oskooie Mol. Divers. 13 2009 395
33. S.R. Kolla, and Y.R. Lee Tetrahedron 66 2010 8938
34. J. Li, Y. Liu, C. Li, and X. Jia Tetrahedron Lett. 50 2009 6502
35. M. Heravi, B. Baghernejad, and H.A. Oskooie Synlett 2009 1123
36. A. Domling Chem. Rev. 106 2006 17
37. S. Marcaccini, and T. Torroba Nat. Protoc. 2 2007 632
38. A. Domling, and I. Ugi Angew. Chem. Int. Ed. 39 2000 3168
39. L.E. Kaim, and L. Grimaud Tetrahedron 65 2009 2153