Conversion of 5-hydroxymethylfurfural to a cyclopentanone derivative by ring rearrangement over supported Au nanoparticles

Chemical Communications

Volumn 50, Issue 42, 2014, Pages 5633-5636

  Ohyama, Junya ^a,b   Kanao, Ryusuke ^a   Esaki, Akihiko ^a   Satsuma, Atsushi ^a,b  

^a NAGOYA UNIVERSITY   (Japan)

^b KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

5-HYDROXYMETHYLFURFURAL; CYCLOPENTANE DERIVATIVE; CYCLOPENTANONE; FURFURAL; GOLD; METAL NANOPARTICLE; 3 HYDROXYMETHYLCYCLOPENTANONE; 5 HYDROXYMETHYLFURFURAL; CYCLOPENTANONE DERIVATIVE; GOLD NANOPARTICLE; LEWIS ACID; METAL OXIDE; NIOBIUM; UNCLASSIFIED DRUG;

CYCLOPENTANES; FURALDEHYDE; GOLD; METAL NANOPARTICLES;

ARTICLE; CONTROLLED STUDY; HYDROGENATION; NANOCATALYSIS; NANOCATALYST; REACTION ANALYSIS; RING REARRANGEMENT;

EID: 84899648083     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc49591d     Document Type: Article

References (26)

1. A. Corma, S. Iborra, A. Velty, Chem. Rev., 2007, 107, 2411
2. J. N. Chheda, G. W. Huber, J. A. Dumesic, Angew. Chem., Int. Ed., 2007, 46, 7164
3. R.-J. van Putten, J. C. van der Waal, E. de Jong, C. B. Rasrendra, H. J. Heeres, J. G. de Vries, Chem. Rev., 2013, 113, 1499
4. N. K. Gupta, S. Nishimura, A. Takagaki, K. Ebitani, Green Chem., 2011, 13, 824
5. J. Ohyama, A. Esaki, Y. Yamamoto, S. Arai, A. Satsuma, RSC Adv., 2013, 3, 1033
6. R. Alamillo, M. Tucker, M. Chia, Y. Pagan-Torres, J. Dumesic, Green Chem., 2012, 14, 1413
7. Y. Nakagawa, K. Tomishige, Catal. Commun., 2010, 12, 154
8. M. Chia, Y. J. Pagan-Torres, D. Hibbitts, Q. Tan, H. N. Pham, A. K. Datye, M. Neurock, R. J. Davis, J. A. Dumesic, J. Am. Chem. Soc., 2011, 133, 12675
9. Y. Roman-Leshkov, C. J. Barrett, Z. Y. Liu, J. A. Dumesic, Nature, 2007, 447, 982
10. J. N. Chheda, J. A. Dumesic, Catal. Today, 2007, 123, 59
11. L. Bui, H. Luo, W. R. Gunther, Y. Román-Leshkov, Angew. Chem., Int. Ed., 2013, 52, 8022
12. Y. Yang, Z. Du, Y. Huang, F. Lu, F. Wang, J. Gao, J. Xu, Green Chem., 2013, 15, 1932
13. S. Sato, J. Igarashi, Y. Yamada, Appl. Catal., A, 2013, 453, 213
14. T. Buntara, S. Noel, P. H. Phua, I. Melián-Cabrera, J. G. de Vries, H. J. Heeres, Angew. Chem., Int. Ed., 2011, 50, 7083
15. M. Hronec, K. Fulajtarova, Catal. Commun., 2012, 24, 100
16. M. Hronec, K. Fulajtarova, T. Liptaj, Appl. Catal., A, 2012, 437-438, 104
17. A. Corma, P. Serna, Science, 2006, 313, 332
18. E. Bus, R. Prins, J. A. van Bokhoven, Catal. Commun., 2007, 8, 1397
19. J. E. Bailie, G. J. Hutchings, Chem. Commun., 1999, 2151
20. J. E. Bailie, H. A. Abdullah, J. A. Anderson, C. H. Rochester, N. V. Richardson, N. Hodge, J.-G. Zhang, A. Burrows, C. J. Kiely, G. J. Hutchings, Phys. Chem. Chem. Phys., 2001, 3, 4113
21. C. Milone, M. L. Tropeano, G. Gulino, G. Neri, R. Ingoglia, S. Galvagno, Chem. Commun., 2002, 868
22. M. Haruta, Catal. Today, 1997, 36, 153
23. Y. Nakagawa, M. Tamura, K. Tomishige, ACS Catal., 2013, 3, 2655
24. J. Ohyama, K. Teramura, S.-I. Okuoka, S. Yamazoe, K. Kato, T. Shishido, T. Tanaka, Langmuir, 2010, 26, 13907
25. K. Nakajima, Y. Baba, R. Noma, M. Kitano, J. N. Kondo, S. Hayashi, M. Hara, J. Am. Chem. Soc., 2011, 133, 4224
26. Y. Koito, K. Nakajima, M. Kitano, M. Hara, Chem. Lett., 2013, 42, 873