Nanoparticle catalysts for nitrile hydration

Coordination Chemistry Reviews

Volumn 280, Issue , 2014, Pages 28-37

  Downs, Emma L ^a   Tyler, David R ^a  

^a UNIVERSITY OF OREGON   (United States)

Author keywords

Amides; Catalysis; Cyanohydrins; Nanoparticles; Nitrile hydration

Indexed keywords

EID: 84906761607     PISSN: 00108545     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ccr.2014.07.029     Document Type: Review

References (55)

1. García-Álvarez R., Crochet P., Cadierno V. Green Chem. 2013, 15:46.
2. Ahmed T.J., Knapp S.M.M., Tyler D.R. Coordin. Chem. Rev. 2011, 255:949.
3. Bullock R.M. Catal. Precious Met. 2010, 51. Wiley-Blackwell, New York.
4. Breno K.L., Ahmed T.J., Pluth M.D., Balzarek C., Tyler D.R. Coordin. Chem. Rev. 2006, 250:1141.
5. Murahashi S.-I., Takaya H. Acc. Chem. Res. 2000, 33:225.
6. Mori K., Yamaguchi K., Mizugaki T., Ebitani K., Kaneda K. Chem. Commun. 2001, 461.
7. Prakash G.K.S., Munoz S.B., Papp A., Masood K., Bychinskaya I., Mathew T., Olah G.A. Asian J. Org. Chem. 2012, 1:146.
8. Gangarajula Y., Gopal B. Chem. Lett. 2012, 41:101.
9. Khadilkar B.M., Madyar V.R. Synth. Commun. 2002, 32:1731.
10. Roy S.C., Dutta P., Nandy L.N., Roy S.K., Samuel P., Pillai S.M., Kaushik V.K., Ravindranathan M. Appl. Catal. 2005, A290:175.
11. Battilocchio C., Hawkins J.M., Ley S.V. Org. Lett. 2014, 16:1060.
12. Yamaguchi K., Wang Y., Kobayashi H., Mizuno N. Chem. Lett. 2012, 41:574.
13. Tamura M., Satsuma A., Shimizu K. Catal. Sci. Technol. 2013, 3:1386.
14. Tamura M., Wakasugi H., Shimizu K., Satsuma A. Chem. Eur. J. 2011, 17:11428.
15. Tamura M., Shimizu K., Satsuma A. Chem. Lett. 2012, 41:1397.
16. Toshima N., Wang Y. Chem. Lett. 1993, 22:1611.
17. Toshima N., Wang Y. Langmuir 1994, 10:4574.
18. Toshima N., Lu P., Wang Y. Preparation, characterization and catalyses of light-transition-metal/noble-metal bimetallic alloy nanoclusters. Studies in Surface Science and Catalysis 2001, 132:243-246.
19. Varma R.S. Pure Appl. Chem. 2013, 85:1703.
20. Polshettiwar V., Varma R.S. Green Chem. 2010, 12:743.
21. Yan N., Xiao C., Kou Y. Coordin. Chem. Rev. 2010, 254:1179.
22. Widegren J.A., Finke R.G. J. Mol. Catal. A: Chem. 2003, 198:317.
23. Stracke J.J., Finke R.G. ACS Catal. 2014, 4:909.
24. Finney E.E., Finke R.G. Inorg. Chim. Acta 2006, 359:2879.
25. Bayram E., Linehan J.C., Fulton J.L., Roberts J.A.S., Szymczak N.K., Smurthwaite T.D., Özkar S., Balasubramanian M., Finke R.G. J. Am. Chem. Soc. 2011, 133:18889.
26. Ishizuka A., Nakazaki Y., Oshiki T. Chem. Lett. 2009, 38:360.
27. Shimizu K., Kubo T., Satsuma A., Kamachi T., Yoshizawa K. ACS Catal. 2012, 2:2467.
28. Subramanian T., Pitchumani K. Catal. Commun. 2012, 29:109.
29. Mitsudome T., Mikami Y., Mori H., Arita S., Mizugaki T., Jitsukawa K., Kaneda K. Chem. Commun. (Camb., U. K.) 2009, 3258.
30. Kim A.Y., Bae H.S., Park S., Park S., Park K.H. Catal. Lett. 2011, 141:685.
31. Shimizu K., Imaiida N., Sawabe K., Satsuma A. Appl. Catal. A 2012, 421-422:114.
32. Sherbow T.J., Downs E.L., Sayler R.I., Razink J.J., Juliette J.J., Tyler D.R. ACS Catal. 2014, (accepted for publication). 10.1021/cs500830s.
33. Woo H., Lee K., Park S., Park K.H. Molecules 2014, 19:699.
34. Liu Y.-M., He L., Wang M.-M., Cao Y., He H.-Y., Fan K.-N. ChemSusChem 2012, 5:1392.
35. Baig R.B.N., Varma R.S. Chem. Commun. 2012, 48:6220.
36. Kumar S., Das P. New J. Chem. 2013, 37:2987.
37. Gawande M.B., Branco P.S., Nogueira I.D., Ghumman C.A.A., Bundaleski N., Santos A., Teodoro O.M.N.D., Luque R. Green Chem. 2013, 15:682.
38. Zhang D., Yang H. J. Mol. Struct. 2014, 1060:1.
39. Zheng J.-N., Lv J.-J., Li S.-S., Xue M.-W., Wang A.-J., Feng J.-J. J. Mater. Chem. A 2014, 2:3445.
40. Sharma S., Ganguly A., Papakonstantinou P., Miao X., Li M., Hutchison J.L., Delichatsios M., Ukleja S. J. Phys. Chem. C 2010, 114:19459.
41. Huang M., Dong G., Wu C., Guan L. Int. J. Hydrogen Energy 2014, 39:4266.
42. E.L. Downs, D.R. Tyler, Unpublished Work.
43. Knapp S.M.M., Sherbow T.J., Yelle R.B., Zakharov L.N., Juliette J.J., Tyler D.R. Organometallics 2013, 32:824.
44. Hirano T., Uehara K., Kamata K., Mizuno N. J. Am. Chem. Soc. 2012, 134:6425.
45. Crestani M.G., Arévalo A., García J.J. Adv. Synth. Catal. 2006, 348:732.
46. Becica J., Jackson A.B., Dougherty W.G., Kassel W.S., West N.M. Dalton Trans. 2014, 43:8738-8748.
47. Meyer F., Hyla-Kryspin I., Kaifer E., Kircher P. Eur. J. Inorg. Chem. 2000, 2000:771.
48. Chetcuti P.A., Knobler C.B., Hawthorne M.F. Organometallics 1988, 7:650.
49. Eisch J.J., Ma X., Han K.I., Gitua J.N., Krüger C. Eur. J. Inorg. Chem. 2001, 2001:77.
50. Sexton B.A., Avery N.R. Surf. Sci. 1983, 129:21.
51. Eustis S., El-Sayed M.A. Chem. Soc. Rev. 2006, 35:209.
52. Knapp S.M.M., Sherbow T.J., Juliette J.J., Tyler D.R. Organometallics 2012, 31:2941.
53. Polshettiwar V., Varma R.S. Chem. Eur. J. 2009, 15:1582.
54. Baig R.B.N., Varma R.S. Green Chem. 2013, 15:398.
55. Garcia-Garrido S.E., Francos J., Cadierno V., Basset J.-M., Polshettiwar V. ChemSusChem 2011, 4:104.