Catalysis in flow: Au-catalysed alkylation of amines by alcohols

Green Chemistry

Volumn 14, Issue 1, 2012, Pages 226-232

  Zotova, Natalia ^a   Roberts, Felicity J ^a   Kelsall, Geoffrey H ^a   Jessiman, Alan S ^b   Hellgardt, Klaus ^a   Hii, King Kuok Mimi ^a  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b PFIZER GLOBAL RESEARCH AND DEVELOPMENT   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84857165582     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/c1gc16118k     Document Type: Article

References (32)

1. P. A. Wender V. A. Verma T. J. Paxton T. H. Pillow Acc. Chem. Res. 2008 41 40-49.
2. T. Newhouse P. S. Baran R. W. Hoffmann Chem. Soc. Rev. 2009 38 3010-3021.
3. P. J. Dunn, A. S. Wells and M. T. Williams, ed., Green Chemistry in the Pharmaceutical Industry, Wiley-VCH, 2010.
4. D. J. C. Constable P. J. Dunn J. D. Hayler G. R. Humphrey J. L. Leazer R. J. Linderman K. Lorenz J. Manley B. A. Pearlman A. Wells A. Zaks T. Y. Zhang Green Chem. 2007 9 411-420.
5. T. D. Nixon M. K. Whittlesey J. M. J. Williams Dalton Trans. 2009 753-762.
6. G. Guillena D. J. Ramon M. Yus Chem. Rev. 2010 110 1611-1641.
7. F. Shi M. K. Tse X. J. Cui D. Gordes D. Michalik K. Thurow Y. Q. Deng M. Beller Angew. Chem., Int. Ed. 2009 48 5912-5915.
8. A. Martinez-Asencio D. J. Ramon M. Yus Tetrahedron Lett. 2010 51 325-327.
9. Y. Zhao S. W. Foo S. Saito Angew. Chem., Int. Ed. 2011 50 3006-3009.
10. J. L. He J. W. Kim K. Yamaguchi N. Mizuno Angew. Chem., Int. Ed. 2009 48 9888-9891.
11. K. Yamaguchi J. L. He T. Oishi N. Mizuno Chem.–Eur. J. 2010 16 7199-7207.
12. J. W. Kim K. Yamaguchi N. Mizuno J. Catal. 2009 263 205-208.
13. P. R. Likhar R. Arundhathi M. L. Kantam P. S. Prathima Eur. J. Org. Chem. 2009 5383-5389.
14. R. Martinez D. J. Ramon M. Yus Org. Biomol. Chem. 2009 7 2176-2181.
15. J. He K. Yamaguchi N. Mizuno Chem. Lett. 2010 39 1182-1183.
16. X. Cui Y. Zhang F. Shi Y. Deng Chem.–Eur. J. 2011 17 1021-1028.
17. C. Della Pina E. Falletta L. Prati M. Rossi Chem. Soc. Rev. 2008 37 2077-2095.
18. L. McEwan M. Julius S. Roberts J. C. Q. Fletcher Gold Bull. 2010 43 298-306.
19. T. Ishida N. Kawakita T. Akita M. Haruta Gold Bull. 2009 42 267-274.
20. A. Corma T. Rodenas M. J. Sabater Chem.–Eur. J. 2010 16 254-260.
21. H. Sun F. Z. Su J. Ni Y. Cao H. Y. He K. N. Fan Angew. Chem., Int. Ed. 2009 48 4390-4393.
22. S. Kegnaes J. Mielby U. V. Mentzel C. H. Christensen A. Riisager Green Chem. 2010 12 1437-1441.
23. L. He X.-B. Lou J. Ni Y.-M. Liu Y. Cao H.-Y. He K.-N. Fan Chem.–Eur. J. 2010 16 13965-13969.
24. N. Zotova K. Hellgardt G. H. Kelsall A. S. Jessiman K. K. Hii Green Chem. 2010 12 2157-2163.
25. M. J. Millan Pharmacol. Ther. 2010 128 229-273.
26. http://www.berkeleymadonna.com/.
27. A. Abad A. Corma H. García Chem.–Eur. J. 2008 14 212-222.
28. C. H. Sun L. M. Liu A. Selloni G. Q. Lu S. C. Smith J. Mater. Chem. 2010 20 10319-10334.
29. V. M. Sanchez E. de la Llave D. A. Scherlis Langmuir 2011 27 2411-2419.
30. 2 attained from other sources such as World Gold Council and donated by Johnson Matthey plc, were also found to be effective under these conditions.
31. ThalesNano Nanotechnology Inc., Graphisoft Park, H-1031 Budapest Zahony u. 7, Hungary (see: http://www.thalesnano.com/products/x-cube).
32. A. J. A. Watson A. C. Maxwell J. M. J. Williams J. Org. Chem. 2011 76 2328-2331.