Asymmetric Hydrogenation
Chapter
Abstract
Inspection of the alkene-metal hydride complex (1) in which the ligand X(SML) is asymmetrically substituted, indicates that steric or polar interaction between the groups S, M and L and the alkene substituents a, b, c, d should discriminate between alternative modes of co-ordination of the alkene i.e. between adducts (1) and (2).
Keywords
Phosphine Oxide Grignard Reagent Optical Yield Rhodium Complex Diethyl Ester
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
Preview
Unable to display preview. Download preview PDF.
References
- 1.L. Horner, H. Winkler, A. Rapp, A. Mentrup, H. Hoffman, and P. Beek: Tetrahedron Letters, 161 (1961).Google Scholar
- 2.M. J. Gallagher and I. D. Jenkins: Topics in Stereochemistry 3, 1 (1968).CrossRefGoogle Scholar
- 3.L. Horner and W. D. Bulzer: Tetrahedron Letters, 1157 (1965).Google Scholar
- 4.W. S. Knowles, M. J. Sabacky, and B. D. Vinyard: Ann. New York Acad. Sci., 1972, 232 (1970).CrossRefGoogle Scholar
- K. Naumann, G. Zon, and K. Mislow: J. Amer. Chem. Soc. 91, 7012 (1969).CrossRefGoogle Scholar
- 5.W. S. Knowles and M. J. Sabacky: J. Chem. Soc. Chem. Comm., 1445 (1968).Google Scholar
- 6.W. S. Knowles, M. J. Sabacky, and B. D. Vineyard: J. Chem. Soc. Chem: Comm., 10 (1972)Google Scholar
- W. S. Knowles, M. J. Sabacky, and B. D. Vineyard: Adv. Chem. Series 132, 274 (1974).Google Scholar
- 7.L. Horner, H. Siegel, and H. Bushe: Angew. Chem. Internat. Edn. 7, 942 (1968).CrossRefGoogle Scholar
- 8.J. D. Morrison, R. E. Burnett, A. M. Aguiar, C. J. Morrow, and C. Phillips: J. Amer. Chem. Soc. 93, 1301 (1971).CrossRefGoogle Scholar
- 9.H. B. Kagan and T. P. Dang: J. Amer. Chem. Soc. 94, 6429 (1972).CrossRefGoogle Scholar
- 10.P. Abley and F. J. McQuillin: J. Chem. Soc. (C), 844 (1971).Google Scholar
- 11.P. H. Boyle and M. T. Keating: J. Chem. Soc. Chem. Comm., 375 (1974).Google Scholar
- 12.R. J. P. Corriu and J. J. E. Moreau: J. Chem. Soc. Chem. Comm., 38 (1973).Google Scholar
- I. Ojima, M. Nihonyanagi, and Y. Nagai: J. Chem. Soc. Chem. Comm., 938 (1972).Google Scholar
- 12y.I. Ojima, T. Rogure, M. Nihonyanagi, and Y. Nagai: Bull. Chem. Soc. Japan 45, 3506 (1972)CrossRefGoogle Scholar
- I. Ojima, M. Nihonyanagi, and Y. Nagai: Bull. Chem. Soc. Japan 45, 3722 (1972)CrossRefGoogle Scholar
- 13.R. J. P. Corriu and J. J. E. Moreau: J. Organomet. Chem. 64, 51 (1974).CrossRefGoogle Scholar
- 14.K. Yamomoto, T. Hayashi, and M. Kumada: J. Organomet. Chem. 54, 45 (1973).CrossRefGoogle Scholar
- 15.P. Bonvicini, A. Levi, G. Modena, and G. Scorrano: J. Chem. Soc. Chem. Comm., 1188 (1972).Google Scholar
- 16.A. Levi, G. Modena, and G. Scorrano: J. Chem. Soc. Chem. Comm., 6 (1975).Google Scholar
- 17.N. Langlois, T.-P. Dang, and H. B. Kagan: Tetrahedron Letters, 4865 (1973).Google Scholar
Copyright information
© D. Reidel Publishing Company, Dordrecht, Holland 1976