Collect. Czech. Chem. Commun.
2000, 65, 717-728
https://doi.org/10.1135/cccc20000717
Diferrocenylphosphine: A Facile Synthesis and Its Use to Prepare Chiral Phosphines
Denis Guillaneux, Lars Martiny and Henri B. Kagan*
Laboratoire de Synthèse Asymétrique (UPRESA 8075), Université Paris-Sud, 91405-Orsay, France
References
1. T., Kumada M.: Acc. Chem. Res. 1982, 15, 395.
<https://doi.org/10.1021/ar00084a003>
2. Kagan H. B., Sasaki M. in: The Chemistry of Organophosphorus Compounds (F. R. Hartley, Ed.), Vol. 1, Chap. 3. J. Wiley and Sons, New York 1990.
3. Hayashi T. in: Ferrocenes (T. Hayashi and A. Togni, Eds), Chap. 2. VCH, Weinheim 1995.
4. Brunner H., Zettlmeier W.: Handbook of Enantioselective Catalysis with Transition Metal Compounds, Volumes I and II. VCH, Weinheim 1993.
5. J. J. A., Lotz M., Knochel P.: Tetrahedron: Asymmetry 1999, 10, 375.
<https://doi.org/10.1016/S0957-4166(99)00002-6>
6a. G. P., Peterson W. R. J. J.: J. Organomet. Chem. 1969, 19, 143.
<https://doi.org/10.1016/S0022-328X(00)87763-3>
6b. M. N., Vilchevskaya V. D., Krylova A. I., Nekrasov Y. S., Tolkunova V. S.: Bull. Acad. Sci. U.S.S.R., Div. Chem. Sci. 1975, 635.
<https://doi.org/10.1007/BF00927502>
7. D., Kagan H. B.: J. Org. Chem. 1995, 60, 2502.
<https://doi.org/10.1021/jo00113a033>
8. T., Oshiki T., Onozawa T., Kusumoto T., Sato K.: J. Am. Chem. Soc. 1990, 112, 5244.
<https://doi.org/10.1021/ja00169a036>
9a. T. P., Kagan H. B.: J. Chem. Soc., Chem. Commun. 1971, 481.
<https://doi.org/10.1039/c29710000481>
9b. T. P., Kagan H. B.: J. Am. Chem. Soc. 1992, 94, 6429.
10. J.: J. Org. Chem. 1989, 54, 509.
<https://doi.org/10.1021/jo00263a052>

