Facile synthesis of a chiral ionic liquid derived from 1-phenylethylamine

Australian Journal of Chemistry

Volumn 60, Issue 1, 2007, Pages 64-67

  Ashraf, Syed A ^a   Pornputtkul, Yingpit ^a   Kane Maguire, Leon A P ^a   Wallace, Gordon G ^a  

^a UNIVERSITY OF WOLLONGONG   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMATOGRAPHY; ELECTROCHEMISTRY; IONIC CONDUCTION; MELTING; NEGATIVE IONS; SALTS; SYNTHESIS (CHEMICAL);

ELECTROCHEMICAL ASYMMETRIC SYNTHESIS; ENANTIOMERIC FORMS; IONIC LIQUIDS;

AMINES;

EID: 33846570447     PISSN: 00049425     EISSN: None     Source Type: Journal    
DOI: 10.1071/CH06384     Document Type: Article

References (23)

1. For excellent recent reviews of room temperature ionic liquids see: (a) T. Welton, Chem. Rev. 1999, 99, 2071. doi:10.1021/CR980032T
2. (b) J. D. Holbrey, K. R. Seddon, Clean Prod. Process. 1999, 1, 223.
3. (c) R. Sheldon, Chem. Commun. 2001, 2399. doi:10.1039/B107270F
4. (d) D. Zhao, M. Wu, Y. Kou, E. Min, Catal. Today 2002, 74, 157. doi:10.1016/80920-5861(01)00541-7
5. (e) J. Dupont, R. F. de Souza, P. A. Z. Suarez, Chem. Rev. 2002, 102, 3667. doi:10.1021/CR010338R
6. (f) S. A. Forsyth, J. M. Pringle, D. R. MacFarlane, Aust. J. Chem. 2004, 57, 113. doi:10.1071/CH03231
7. M. J. Earle, K. R. Seddon, Pure Appl. Chem. 2000, 72, 1391.
8. (a) J. S. Wilkes, Green Chem. 2002, 4, 73. doi:10.1039/B110838G
9. (b) J. S. Wilkes, J. Mol. Catal. 2004, 214, 11. doi:10.1016/J.MOLCATA.2003.11.029
10. W. Lu, A. G. Fadeev, B. Qi, E. Smela, B. R. Mattes, J. Ding, G. M. Spinks, J. Mazurkiewicz, D. Zhao, G. G. Wallace, D. R. MacFarlane, S. A. Forsyth, M. Forsyth, Science 2002, 297, 983. doi:10.1126/SCIENCE.1072651
11. J. H. Mazurkiewicz, P. C. Irmis, G. G. Wallace, D. R. MacFarlane, M. Forsyth, Synth. Met. 2003, 135-136, 31. doi:10.1016/S0379-6779(02)00688-4
12. W. Lu, A. G. Fadeev, B. Qi, T. Pestalozzi-Conely, B. R. Mattes, Synth. Met. 2003, 135-136, 139. doi:10.1016/80379-6779(02)00558-1
13. J. Ding, D. Zhou, G. Spinks, S. Forsyth, M. Forsyth, D. MacFarlane, Chem. Mater. 2003, 15, 2392. doi:10.1021/CM020918K
14. C. Baudequin, D. Brégeon, J. Levillain, F. Guillen, J.-C. Plaquevent, A.-C. Gaumont, Tetrarahedron: Asymmetry 2005, 16, 3921. doi:10.1016/J.TETASY.2005.10.026
15. J. Howarth, K. Hanlon, D. Fayne, P. McCormac, Tetrahedron Lett. 1997, 38, 3097. doi:10.1016/80040-4039(97)00554-6
16. Y. Ishida, H. Miyauchi, K. Saigo, Chem. Commun. 2002, 2240. doi:10.1039/B206495B
17. W. Bao, Z. Wang, Y. Li, J. Org. Chem. 2003, 68, 591. doi:10.1021/JO020503I
18. P. Wasserscheid, A. Bösmann, C. Bolm, Chem. Commun. 2002, 200. doi:10.1039/B109493A
19. M. J. Earle, P. B. McCormac, K. R. Sneddon, Green Chem. 1999, 1, 23. doi:10.1039/A808052F
20. H. L. Ngo, K. LeCompte, L. Hargens, A. B. McEwen, Thermochim. Acta 2000, 357-358, 97. doi:10.1016/80040-6031(00)00373-7
21. P. Bonhôte, A.-P. Dias, N. Papageorgiou, K. Kalyanasundaram, M. Grätzel, Inorg. Chem. 1996, 35, 1168. doi:10.1021/IC951325X
22. Y. Pornputtkul, L. A. P. Kane-Maguire, G. G. Wallace, J. Electrochem. Soc., submitted.
23. J. G. Huddleston, A. E. Visser, W. M. Reichert, H. D. Willauer, G. A. Broker, R. D. Rogers, Green Chem. 2001, 3, 156, and references therein, doi:10.1039/B103275P