General and selective reductive amination of carbonyl compounds using a core-shell structured Co3O4/NGr@C catalyst

Green Chemistry

Volumn 16, Issue 10, 2014, Pages 4535-4540

  Stemmler, Tobias ^a   Westerhaus, Felix A ^a   Surkus, Annette Enrica ^a   Pohl, Marga Martina ^a   Junge, Kathrin ^a   Beller, Matthias ^a  

^a UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84907755902     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/c4gc00536h     Document Type: Article

References (55)

1. P. N. Rylander, Hydrogenation Methods, Academic Press, New York, 1985, pp. 82-93
2. O. Mitsunobu, B. M. Trost and I. Fleming, Comprehensive Organic Synthesis, Oxford, 1991, vol. 6, p. 65
3. S. Nishimura, Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis, Wiley-VCH, New York, 2001, pp. 170-290
4. F. Nerozzi Platinum Met. Rev. 2012 56 236 241
5. K. Shimizu M. Nishimura A. Satsuma ChemCatChem 2009 1 497 503
6. K. Yamaguchi J. L. He T. Oishi N. Mizuno Chem.-Eur. J. 2010 16 7199 7207
7. P. R. Likhar R. Arundhathi M. L. Kantam P. S. Prathima Eur. J. Org. Chem. 2009 5383 5389
8. J. W. Kim K. Yamaguchi N. Mizuno J. Catal. 2009 263 205 208
9. J. L. He K. Shimizu N. Mizuno Chem. Lett. 2010 39 1182 1183
10. L. Li Z. Niu S. Cai Y. Zhi H. Li H. Rong L. Liu L. Liu W. He Y. Li Chem. Commun. 2013 49 6843 6845
11. C.-H. Tang L. He Y.-M. Liu Y. Cao H.-Y. He K.-N. Fan Chem.-Eur. J. 2011 17 7172 7177
12. B. Sreedhar P. S. Reddy D. K. Devi J. Org. Chem. 2009 74 8806 8809
13. U. Siegrist, P. Baumeister and H.-U. Blaser, Catalysis of Organic Reactions, ed., F. Herkes, M. Dekker, Chemical Industries Series 75, 1998, pp. 207-219
14. A. Onopchenko E. T. Sabourin C. M. Selwitz J. Org. Chem. 1979 44 1233 1236
15. P. Baumeister H. U. Blaser W. Scherrer Stud. Surf. Sci. Catal. 1991 59 312
16. E. Auer, A. Freud, M. Gross, R. Hartung and P. Panster, Catalysis of Organic Reactions, ed., F. Herkes, M. Dekker, Chemical Industries Series 75, 1998, pp. 225-231
17. F. Cardenas-Lizana S. Gomez-Quero M. A. Keane ChemSusChem 2008 1 215 221
18. F. Cardenas-Lizana S. Gomez-Quero A. Hugon L. Delannoy C. Louis M. A. Keane J. Catal. 2009 262 235 243
19. M. Takasaki Y. Motoyama K. Higashi S.-H. Yoon I. Mochida H. Nagashima Org. Lett. 2008 10 1601 1604
20. C.-H. Li Z.-X. Yu J. Mol. Catal. A: Chem. 2005 226 101 105
21. G. G. Ferrier F. King Platinum Met. Rev. 1983 27 72 77
22. R. Raja V. B. Golovko J. M. Thomas A. Berenger-Murcia W. Z. Zhou S. H. Xie B. F. G. Johnson Chem. Commun. 2005 2026 2028
23. L. P. Kuhn J. Am. Chem. Soc. 1951 73 1510 1512
24. H. Greenfield F. S. Dovell J. Org. Chem. 1967 32 3670 3671
25. C. F. H. Allen J. van Allan Org. Synth. Coll. 1955 3 63
26. J. Xiong J. Chen J. Zhang Catal. Commun. 2007 8 345 350
27. H. U. Blaser, U. Siegrist, H. Steiner and M. Studer, Aromatic nitro compounds: Fine Chemicals through Heterogeneous Catalysis, ed., R. A. Sheldon, and, H. van Bekkum, Wiley-VCH, Weinheim, 2001, p. 389
28. E. Iglesia Appl. Catal., A 1997 161 59 78
29. A. Y. Khodakov W. Chu P. Fongarland Chem. Rev. 2007 107 1692 1744
30. B. H. Davis Top. Catal. 2005 32 143 168
31. S. L. Soled E. Iglesia R. A. Fiato J. E. Baumgartner H. Vroman S. Miseo Top. Catal. 2003 26 101 109
32. M. Shelef Chem. Rev. 1995 95 209 225
33. B. Wichterlova Top. Catal. 2004 28 131 140
34. S. Vetrivel A. Pandurangam J. Mol. Catal. A: Chem. 2005 227 269 272
35. J. Pielichowski G. Kowalski Mol. Cryst. Liq. Cryst. 2010 522 405 411
36. D. Banerjee R. V. Jagadeesh K. Junge M.-M. Pohl J. Radnik A. Brückner M. Beller Angew. Chem., Int. Ed. 2014 53 4359 4363
37. R. J. Farrauto and C. H. Bartholomew, Fundamental of Industrial Catalytic Processes, Blackie Academic and Professional, London, 1997, pp. 640-644
38. D. Burri K.-W. Jun Y.-H. Kim J. M. Kim S.-E. Park J. S. Yoo Chem. Lett. 2002 31 212 214
39. J. Spivey J. Butt Catal. Today 1992 11 465 500
40. T. V. Choudhary S. Banerjee V. R. Choudhary Appl. Catal., A 2002 234 1 24
41. F. Grillo M. M. Natile A. Glisenti Appl. Catal., B 2004 48 267 274
42. Y. J. Mergler J. Hoebink B. E. Nieuwenhuys J. Catal. 1999 167 305 313
43. K. Bourikas C. Kordulis J. Vakros A. Lycourghiotis Adv. Colloid Interface Sci. 2004 110 97 120
44. H. Li S. Wang F. Ling J. Li J. Mol. Catal. A: Chem. 2006 244 33 40
45. A. Y. Khodakov A. Griboval-Constant R. Bechara F. Villain J. Phys. Chem. B 2001 105 9805 9811
46. F. A. Westerhaus R. V. Jagadeesh G. Wienhöfer M.-M. Pohl J. Radnik A.-E. Surkus J. Rabeah K. Junge H. Junge M. Nielsen A. Brückner M. Beller Nat. Chem. 2013 5 537 543
47. A. Bencini V. Lippolis Coord. Chem. Rev. 2010 254 2096 2180
48. J. H. Zagal, F. Bedioui and J.-P. Dodelet, N4-Macrocyclic Metal Complexes, Springer Science+Business Media, Inc., New York, 2006, pp. 83-126
49. A. Corma H. Garcia Chem. Rev. 2010 8 4606 4655
50. J. Volf and J. Pasek, in Catalytic Hydrogenation, ed., L. Cerveny, Elsevier, Amsterdam, 1986, vol. 27, pp. 105-144
51. S. Sato T. Sakamoto E. Miyazawa Y. Kikugawa Tetrahedron 2004 60 7899 7906
52. F. Santoro R. Psaro N. Ravasio F. Zaccheria ChemCatChem 2012 4 1249 1254
53. E. J. Schwoegler H. Adkins J. Am. Chem. Soc. 1939 61 3499 3502
54. F. Qi L. Hu S. Lu X. Cao H. Gu Chem. Commun. 2012 48 9631 9633
55. O. Saidi A. J. Blacker M. M. Farah S. P. Marsden J. M. Williams Angew. Chem., Int. Ed. 2009 48 7375