Page 63 - Catalysts for Fine Chemical Synthesis Vol 1 - Robert & Poignant

46 hydrolysis, oxidation and reduction

Schaus, S.E., Branalt, J. and Jacobsen, E.N. J. Org. Chem., 1998, 63, 403) can be
catalysed using chiral organometallic systems.
142. Johannsen, M. and Jogensen, K.A. Tetrahedron, 1996, 52, 7321. (The organochro-
mium catalysts invented by Jacobsen are also noteworthy, see Thompson, C.F.,
Jamison, T.F. and Jacobsen, E.N. J. Am. Chem. Soc., 2000, 122, 10482.)
143. Esikova, I.A., Nahreini, T.S. and O'Donnell, M.J. in Phase-Transfer Catalysis (M.
Halpern, ed.), ACS (ACS Symposium Series), Washington, 1997, pp 89±96.
144. a) Casalnuovo, A.L. and Rajan Babu, T.V. J. Am. Chem. Soc., 1994, 116, 9869;
idem, `The Asymmetric Hydrocyanation of Vinyl Arenes' in Chirality and Industry
II (eds Collins, A.N., Sheldrake, G.N. and Crosby, J.) Wiley, New York, 309.
145. Krueger, C.A., Kuntz, K.W., Drierba, C.D., Wirschun, W.G., Gleason, J.D.,
Snapper, M.L. and Hoveyda, A.H. J. Am. Chem. Soc., 1999, 121, 4284.
146. Agbossou, F., Carpentier, J.-F. and Mortreux, A. Chem. Rev., 1995, 95, 2485;
Herrmann, W.A. and Cornils, B. Angew. Chem. Int. Ed. Eng., 1997, 36, 1048; I.
To Äth, Elsevier, C.J., de Vries, J.G., Bakos, J., Smeets, W.J.J. and Spek, A.L. J.
Organomet. Chem., 1997, 540, 15.
147. Sakai, N., Mano, S., Nozaki, K. and Takaya, H. J. Am. Chem. Soc., 1993, 115,
7033; Nozaki, K., Sakai, N., Nanno, T., Higashijima, T., Mano, S., Horiuchi, T.
and Takaya, H. ibid, 1997, 119, 4413.
148. Alper, H. and Hamel, N. J. Am. Chem. Soc., 1990, 112, 2803; Zhou, H., Hou, J.,
Chen, J., Lu, S., Fu, H. and Wang, H. J. Organomet. Chem., 1997, 543, 227.
149. Nomura, N., Jin, J., Park, H. and Rajan Babu, T.V. J. Am. Chem. Soc., 1998, 120,
459.
150. Bayersdo Èrfer, R., Ganter, B., Englert, U., Keim, W. and Vogt, D. J. Organomet.
Chem., 1998, 552, 187.
151. Aratani, T. Pure Appl. Chem., 1985, 57, 1839.
152. Doyle, M.P., McKervey, M.A. and Ye, T. Modern Catalytic Methods for Organic
Synthesis with Diazo Compounds, John Wiley and Sons, New York, 1998; Lo,
M.M-C. and Fu, G.C. J. Am. Chem. Soc. 1998, 120, 10270.
153. Fukuda, T. and Katsuki, T. Tetrahedron, 1997, 53, 7201.
154. Ishitani, H. and Achiwa, K. Synlett, 1997, 781; Uchida, T., Irie, R. and Katsuki, T.
ibid, 1999, 1163; Niimi, T., Uchida, T., Irie, R. and Katsuki, T. Tetrahedron Lett.,
2000 41, 3647.
155. Antilla, J.C. and Wulff, W.D. J. Am. Chem. Soc., 1999, 121, 5099.
156. Trost, B.M. and Hachiya, I. J. Am. Chem. Soc., 1998, 120, 1104.
157. Trost, B.M. and van Vranken D.L. Chem. Rev., 1996, 96, 395; Trost., B.M. Acc.
Chem. Res., 1996, 29, 355; Tye, H. J.C.S. Perkin Trans. 1, 2000, 284; see also
Hamada, Y., Seto, N., Takayanagi, Y., Nakano, T. and Hara, O. Tetrahedron
Lett., 1999, 40, 7791.
158. Sears, P. and Wong, C.-H. J.C.S., Chem. Commun., 1998, 1161.
159. Takayama, S., McGarvey, G.J. and Wong, C.-H. Chem. Soc. Rev., 1997, 26, 407.
160. Blixt, O. and Norberg, T. J. Org. Chem., 1998, 63, 2705.
161. The work of Williams and Ba Èckvall provide a foretaste of possibilities in this
general area see Persson, B.A., Larsson, A.L.E., Le Ray, M. and Ba Èckvall, J.-E.
J. Am. Chem. Soc., 1999, 121, 1645; Allen, J.V. and Williams, J.M.J. Tetrahedron
Lett., 1996, 37, 1859.
162. For example see Biomimetic Oxidations Catalysed by Transition Metal Complexes,
Meunier, B. World Scientific Publishing, Imperial College, London, 2000.