Page 59 - Catalysts for Fine Chemical Synthesis Vol 1 - Robert & Poignant

42 hydrolysis, oxidation and reduction

47. Tas, D., Thoelen, C., Vanekelecom, I.F.J. and Jacobs, P.A. J.C.S., Chem. Commun.,
1997, 2323.
48. Kitamura, M., Ohkuma, T., Inoue, S., Sayo, N., Kumobayashi, H., Akutagawa, S.,
Ohta, T., Takayon, H. and Norori, R. J. Am. Chem. Soc., 1988, 110, 629.
49. Kawano, H., Ishii, Y., Saburi, M. and Uchida, Y. J.C.S. Chem. Commun., 1988, 87.
50. Arrigo, P.D., Fuganti, C., Fantoni, G.P. and Servi, S. Tetrahedron, 1998, 54, 15017.
51. Aleu, J., Fronza, G., Fuganti, C., Perozzo, V. and Serra, S. Tetrahedron: Asym-
metry, 1998, 9, 1589.
52. Kawai, Y., Haynshi, M., Inaba, Y., Saitou, K. and Ohno, A. Tetrahedron Lett.,
1998, 39, 5225; Kawai, Y., Saitou, K., Hida, K., Dao, D.H. and Ohno, A. Bull.
Chem. Soc., Japan, 1996, 69, 2633.
53. Ferraboschi, P., Elahi, S.R.T., Verza, E., Meroni-Rivolla, F. and Santaniello, E.
Synlett, 1996, 1176.
54. Leuenberger, H.G.W., Boguth, W., Barner, R., Schmid, M. and Zell, R. Helv. Chim.
Acta., 1979, 62, 455.
55. Matsumoto, K., Kawabata, Y., Takahashi, J., Fujita, Y. and Hatanaka, M. Chem.
Lett., 1998, 283.
56. Homogeneous Catalysis Parshall, G.W. and Ittel, S.D. (eds), 1992 (second edition),
Wiley, New York, p 33; Takaya, H., Ohta, T. and Noyori, R. Catalytic Asymmetric
Synthesis Chapter 1, VCH, Weinheim, 1993.
57. Ikariya, T., Ishii, Y., Kawano, H., Arai, T., Saburi, M., Yoshikawa, S. and Akuta-
gawa, S. J.C.S., Chem. Commun., 1985, 922.
58. Noyori, R. Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994.
59. Kitamura, M., Hsiao, Y., Noyori, R. and Takaya, H. Tetrahedron Lett., 1987, 28,
4829.
60. Kitamura, M., Hsiao, Y., Ohta, M., Tsukamoto, M., Ohta, T., Takaya, H. and
Noyori, R. J. Org. Chem., 1994, 59, 297.
61. Uemura, T., Zhang, X.Y., Matsumura, K., Sayo, N., Kumobayashi, H., Ohta, T.,
Nozaki, K. and Takaya, H. J. Org. Chem., 1996, 61, 5510; a classical example is the
Monsanto synthesis of (l)-DOPA using ruthenium complexed with the diphosphine
DIPAMP, see Classics in Total Synthesis, Nicolaou, K.C. and Sorensen, E.J. VCH,
Weinheim, 1996.
62. Dwars, T., Schmidt, U., Fischer, C., Grassert, I., Kempe, R., Fro Èlich, R., Drauz, K.
and Oehme, G. Angew. Chem. Int. Ed, 1998, 37, 2851.
63. Burk, M.J., Gross, M.F. and Martinez, J.P. J. Am. Chem. Soc., 1995, 117, 9375; see
also Burk, M.J., Allen, J.G. and Kiesman, W.F. J. Am. Chem. Soc., 1998, 120, 657;
for the asymmetric reduction of a variety of b-substituted esters using rhodium/
ligand complexes of this type see Burk, M.J., Bienewald, F., Harris, M. and Zanotti-
Gerosa, A. Angew Chem. Int. Ed. Engl., 1998, 37, 1931.
64. Boaz, N.W. Tetrahedron Lett., 1998, 39, 5505; see also Zhu, G., Casalnuova, A.L.
and Zhang, X. J. Org. Chem., 1998, 63, 8100.
65. Reetz, M.T., Gosberg, A., Goddard, R. and Kyung, S.-H. J.C.S. Chem. Comm.
1998, 2077; Kang, J., Lee, J.H., Ahn, S.H. and Choi, J.S. Tetrahedron Lett., 1998,
39, 5523; Perea, J.J.A., Borneo, A. and Knochel, P. ibid, 1998, 39, 8073.
66. Chan, A., Hu, W.H., Pai, C.C., Lau, C.P., Jiang, Y.Z., Mi, A.Q., Yan, M., Sun, J.,
Lou, R.L. and Deng, J.G. J. Am. Chem. Soc., 1997, 119, 9570.
67. Rajan Babu, T.V., Ayers, T.A., Halliday, G.A., You, K.K. and Calabrese, J.C. J. Org.
Chem., 1997, 62, 6012; Selke, R., Ohff, M. and Riepe, A. Tetrahedron, 1996, 52,
15079.