1 |
T. Welton, "Room-temperature ionic liquids. Solvent for synthesis and catalysis", Chem. Rev., Vol. 99, pp. 2071-2083, 1999.
DOI
ScienceOn
|
2 |
P. Wasserscheid and K. Wilhelm, "Ionic liquids-new solution for transition metal catalysis", Angew. Chem. Int. Edt., Vol. 39, pp. 3772-3789, 2000.
DOI
|
3 |
R. M. Lau, F. V. Rantwijk, K. R. Seddon, and R. A. Sheldon, "Lipase-catalyzed reactions in ionic liquids", Org. Lett., Vol. 2, pp. 4189-4191, 2000.
DOI
ScienceOn
|
4 |
K.-W. Kim, B. Y. Song, M.-Y. Choi, and M.-J. Kim, "Biocatalysis in ionic liquid: markedly enhanced enantioselectivity of lipase", Org. Lett., Vol. 3, pp. 1507-1509, 2001.
DOI
ScienceOn
|
5 |
B. List, R. A. Lerner, and C. F. Barbas III, "Prolinecatalyzed direct asymmetric aldol reactions", J. Am. Chem. Soc., Vol. 122, pp. 2395-2396, 2000.
DOI
ScienceOn
|
6 |
K. Sakthivel, W. Notz, T. Bui, and C. F. Barbas III. "Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions", J. Am. Chem. Soc., Vol. 123, pp. 5260-5267, 2001.
DOI
ScienceOn
|
7 |
T. D. Machajewski and C.-H. Wong, "The catalytic asymmetric aldol reaction", Angew. Chem. Int. Edt., Vol. 39, pp. 1352-1375, 2000.
DOI
|
8 |
J. Wabner, R. A. Lerner, and C. F. Barbas III, "Efficient aldolase catalytic antibodies that use the enamine mechanism of natural enzyme", Science, Vol. 270, pp. 1797-1800, 1995.
DOI
ScienceOn
|