Reductive amination of aldehydes and ketones catalyzed by deep eutectic solvent using sodium borohydride as a reducing agent

Journal of Molecular Liquids

Volumn 196, Issue , 2014, Pages 208-210

  Saberi, Dariush ^a   Akbari, Jafar ^a   Mahdudi, Samaneh ^a   Heydari, Akbar ^a  

^a TARBIAT MODARES UNIVERSITY   (Iran)

Author keywords

ChCl Urea; Deep eutectic solvents; Green catalyst; Reductive amination; Secondary amines

Indexed keywords

BIOCOMPATIBILITY; CATALYSTS; KETONES; SODIUM;

CHCL/UREA; DEEP EUTECTIC SOLVENTS; GREEN CATALYSTS; REDUCTIVE AMINATION; SECONDARY AMINES;

AMINES;

EID: 84899112097     PISSN: 01677322     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molliq.2014.03.024     Document Type: Article

References (47)

1. Q. Zhang, K.D.O. Vigier, S. Royer, and F. Jérôme Chem. Soc. Rev. 41 2012 7108
2. M. Francisco, A.V.D. Bruinhorst, and M.C. Kroon Angew. Chem. Int. Ed. 52 2013 3074
3. Y.A. Sonawane, S.B. Phadtare, B.N. Borse, A.R. Jagtap, and G.S. Shankarling Org. Lett. 12 2010 1456
4. A.P. Abbott, T.J. Bell, S. Handa, and B. Stoddart Green Chem. 7 2005 705
5. R.C. Morales, V. Tambyrajah, P.R. Jenkins, D.L. Davies, and A.P. Abbott Chem. Commun. 2 2004 158
6. N. Azizi, E. Batebi, S. Bagherpour, and H. Ghafuri RSC Adv. 2 2012 2289
7. J. Ward, and R. Wohlgemuth Curr. Org. Chem. 14 2010 1914
8. E. Byun, B. Hong, K.A.D. Castro, M. Lim, and H. Rhee J. Org. Chem. 72 2007 9815
9. F. Nador, Y. Moglie, A. Ciolino, A. Pierini, V. Dorn, M. Yus, F. Alonso, and G. Radivoy Tetrahedron Lett. 53 2012 3156
10. H. Choi, and M.P. Doyle Chem. Commun. 7 2007 745
11. X. Lang, H. Ji, C. Chen, W. Ma, and J. Zhao Angew. Chem. Int. Ed. 50 2011 3934
12. C.S. Yi, and D.W. Lee Organometallics 28 2009 947
13. M. Largeron, A. Chiaroni, and M.B. Fleury Chem. Eur. J. 14 2008 996
14. G. Jiang, J. Chen, J.S. Huang, and C.M. Che Org. Lett. 11 2009 4568
15. I. Saxena, R. Borah, and J.C. Sarma J. Chem. Soc. Perkin Trans. 1 2000 503
16. S. Bhattacharyya J. Org. Chem. 60 1995 4928
17. H. Alinezhad, and E. Ardestani Lett. Org. Chem. 4 2007 473
18. S. Bhattacharyya Synth. Commun. 1997 4265
19. A. Heydari, A. Arefi, and M. Esfandyari J. Mol. Catal. A 274 2007 169
20. M.J. Bhanushali, N.S. Nandurkar, M. Bhor, and B.M. Bhanag Tetrahedron Lett. 48 2007 1273
21. M.D. Bomann, I.C. Guch, and M. Dimare J. Org. Chem. 60 1995 5995
22. A. Pelter, R.M. Rosser, and S. Mills J. Chem. Soc. Perkin Trans. 1 1984 717
23. H. Firouzabadi, N. Iranpoor, and H. Alinezhad Bull. Chem. Soc. Jpn. 76 2003 143
24. H. Alinezhad, M. Tajbakhsh, and F. Salehian Synlett 2005 170
25. H. Alinezhad, M. Tajbakhsh, and R. Zamani Synlett 2006 431
26. A. Heydari, S. Khaksar, M. Esfandyari, and M. Tajbakhsh Tetrahedron 63 2007 3363
27. R.Y. Lai, C.I. Lee, and S.T. Liu Tetrahedron 64 2008 1213
28. P.S. Reddy, S. Kanjilal, S. Sunitha, and R.B.N. Prasad Tetrahedron Lett. 48 2007 8807
29. C.F. Lane Synthesis 1975 135
30. A.F. Abdel-Magid, K.G. Carsone, B.D. Harris, C.A. Maryanoff, and R.D. Shah J. Org. Chem. 61 1996 3849
31. J.R. Bernardo, S.C.A. Sousa, P.R. Florindo, M. Wolff, B. Machura, and A.N. Fernandes Tetrahedron 69 2013 9145
32. Q.P.B. Nguyen, and T.H. Kim Tetrahedron 69 2013 4938
33. N.U. Kumar, B.S. Reddy, V.P. Reddy, and R. Bandichhor Tetrahedron Lett. 53 2012 4354
34. F. Nador, Y. Moglie, A. Ciolino, A. Pierini, V. Dorn, M. Yus, F. Alonso, and G. Radivoy Tetrahedron Lett. 53 2012 3156
35. G.N. Karageorge, and J.E. Macor Tetrahedron Lett. 52 2011 5117
36. Q.P.B. Nguyen, and T.H. Kim Tetrahedron Lett. 52 2011 5004
37. R. Cano, M. Yus, and D. Ramón J. Tetrahedron 67 2011 8079
38. J. Zheng, T. Roisnel, C. Darcel, and J.B. Sortais ChemCatChem 5 2013 2861
39. R. Hiroi, N. Miyoshi, and M. Wada Chem. Lett. 2002 274
40. S. Kobayashi, M. Yasuda, and I. Hachiya Chem. Lett. 1996 407
41. B.-C. Chen, J.E. Sundeen, P. Guo, M.S. Bednarz, and R. Zhao Tetrahedron Lett. 42 2001 1245
42. T. Suwa, E. Sugiyama, I. Shibata, and A. Baba Synthesis 2000 558
43. I.V. Micc'ovic', M.D. Ivanovic', D.M. Piatak, and V.D. Bojic' Synthesis 1991 1043
44. R.M. Lopez, and G.C. Fu Tetrahedron 53 1997 16349
45. A.P. Abbott, G. Capper, D.L. Davies, R.K. Rasheed, and V. Tambyrajah Chem. Commun. 2003 70
46. B. Singh, H. Lobo, and G. Shankarling Catal. Lett. 141 2011 178
47. A. Zhu, T. Jiang, B. Han, J. Zhang, Y. Xie, and X. Ma Green Chem. 9 2007 169.