Clean, reusable and low cost heterogeneous catalyst for amide synthesis

Chemical Communications

Volumn , Issue 18, 2009, Pages 2562-2564

  Comerford, James W ^a   Clark, James H ^a   MacQuarrie, Duncan J ^a   Breeden, Simon W ^a  

^a UNIVERSITY OF YORK   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; AMINE; LEWIS ACID; SILICON DIOXIDE; ZEOLITE;

AMIDATION; ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; COST BENEFIT ANALYSIS; HYDROPHOBICITY; SYNTHESIS;

EID: 65349151305     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b901581g     Document Type: Article

References (22)

1. F. Albericio Curr. Opin. Chem. Biol. 2004 8 211 221
2. A. Rimola S. Tosoni M. Sodupe P. Ugliengo Chem. Phys. Lett. 2005 408 4-6 295 301
3. 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
4. C. Schotten Ber. Dtsch. Chem. Ges. 1884 17 2544
5. A. J. Pearson and W. R. Roush, Handbook of Reagents for Organic Synthesis: Activating Agents and Protecting Groups, Wiley, New York, 1999, pp. 370-373
6. L. A. Carpino J. Am. Chem. Soc. 1993 115 4397 4398
7. W. L. Scott (Eli Lilly and Company), US Pat., 6362351, 2002
8. K. A. Mahmoud Y. T. Long G. Schatte H. B. Kraatz Eur. J. Inorg. Chem. 2005 173 180
9. T. Schlama V. Gouverneur C. Mioskowski Tetrahedron Lett. 1996 37 39 7047 7048
10. C. A. G. N. Montalbetti V. Falque Tetrahedron 2005 61 10827 10852
11. R. Paul G. W. Anderson J. Am. Chem. Soc. 1960 82 17 4596 4600
12. P. G. Urben, Brethericks Handbook of Reactive Chemical Hazards, Butterworth-Heinemann, Oxford, UK, 1999, p. 746
13. K. Ishihara S. Ohara H. Yamamoto J. Org. Chem. 1996 61 4196 4197
14. K. Ishihara S. Ohara H. Yomamoto Macromolecules 2000 33 3511 3513
15. T. Maki K. Ishihara H. Yamamoto Org. Lett. 2006 8 7 1431 1434
16. K. Arnold A. S. Batsanov B. Davies A. Whiting Green Chem. 2008 10 124 134
17. S. W. Coghlan R. L. Giles J. A. K. Howard L. G. F. Patrick M. R. Probert G. E. Smith A. Whiting J. Organomet. Chem. 2005 690 21-22 4784 4793
18. R. M. Al-Zoubi O. Marion D. G. Hall Angew. Chem., Int. Ed. 2008 47 2876 2879
19. Fluka K60 silica, particle size 0.035-0.070 mm, mesh 220-440
20. E. F. Vansant, P. Van Der Voort and K. C. Vrancken, Characterization and Chemical Modification of the Silica Surface, Elsevier Science, Amsterdam, 1995, pp. 62-65
21. K. H. Bourne F. R. Cannings R. C. Pitkethly J. Phys. Chem. 1970 74 2197 2205
22. R. A. Sheldon Chem. Commun. 2008 3352 3365