Collect. Czech. Chem. Commun. 2002, 67, 1700-1708
https://doi.org/10.1135/cccc20021700

Derivatives of (S)-{[2-(Methoxymethyl)pyrrolidin-1-yl]methyl}ferrocene - New Planar Chiral Ligands

Radovan Šebesta* and Marta Sališová

Department of Organic Chemistry, Faculty of Natural Sciences, Comenius University, Mlynská dolina, 842 15 Bratislava, Slovak Republic

References

1. Togni A., Hayashi T.: Ferrocenes, Homogenous Catalysis, Organic Synthesis, Materials Science. VCH, Weinheim 1995.
2. Richards C. J., Locke A. L.: Tetrahedron: Asymmetry 1998, 9, 2377. <https://doi.org/10.1016/S0957-4166(98)00251-1>
3. Hayashi T., Kumada M.: Acc. Chem. Res. 1982, 15, 395. <https://doi.org/10.1021/ar00084a003>
4a. Noyori R., Kitamura M.: Angew. Chem., Int. Ed. Engl. 1991, 30, 49. <https://doi.org/10.1002/anie.199100491>
4b. Soai K., Niwa S.: Chem. Rev. (Washington, D. C.) 1992, 92, 833. <https://doi.org/10.1021/cr00013a004>
4c. Pu L., Yu H.-B.: Chem. Rev. (Washington, D. C.) 2001, 101, 757. <https://doi.org/10.1021/cr000411y>
5. Watanabe M., Araki S., Butsugan Y., Uemura M.: J. Org. Chem. 1991, 56, 2218. <https://doi.org/10.1021/jo00006a048>
6a. Bolm C., Muniz-Fernandez K., Seger A., Raabe G., Gunther K.: J. Org. Chem. 1998, 63, 7860. <https://doi.org/10.1021/jo981098r>
6b. Deng W.-P., Hou X.-L., Dai L.-X.: Tetrahedron: Asymmetry 1999, 10, 4689. <https://doi.org/10.1016/S0957-4166(99)00512-1>
6c. Zhang W., Yoshinaga H., Imai Y., Kida T., Nakatsuji Y., Ikeda I.: Synlett 2000, 1512.
7a. Marquarding D., Klusacek H., Gokel G., Hoffmann P., Ugi I.: J. Am. Chem. Soc. 1970, 92, 5389. <https://doi.org/10.1021/ja00721a017>
7b. Ganter C., Wagner T.: Chem. Ber. 1995, 128, 1157. <https://doi.org/10.1002/cber.19951281204>
8a. Sammakia T., Latham H. A., Schaad D. R.: J. Org. Chem. 1995, 60, 10. <https://doi.org/10.1021/jo00106a005>
8b. Richards C. J., Damalidis T., Hibbs D. E., Hursthouse M. B.: Synlett 1995, 74. <https://doi.org/10.1055/s-1995-4864>
8c. Nishibayashi Y., Uemura S.: Synlett 1995, 79. <https://doi.org/10.1055/s-1995-4881>
9. Riant O., Samuel O., Kagan H. B.: J. Am. Chem. Soc. 1993, 115, 5835. <https://doi.org/10.1021/ja00066a066>
10. Enders D., Peters R., Lochtman R., Raabe G., Runsink J., Bats J. W.: Eur. J. Org. Chem. 2000, 3399. <https://doi.org/10.1002/1099-0690(200010)2000:20<3399::AID-EJOC3399>3.0.CO;2-D>
11. Rebiere F., Riant O., Ricard L., Kagan H. B.: Angew. Chem., Int. Ed. Engl. 1993, 32, 568. <https://doi.org/10.1002/anie.199305681>
12. Kitamura M., Suga S., Kawai K., Noyori R.: J. Am. Chem. Soc. 1986, 108, 6071. <https://doi.org/10.1021/ja00279a083>
13. Xiao L., Mereiter K., Weissensteiner W., Widhalm M.: Synthesis 1999, 1354. <https://doi.org/10.1055/s-1999-3548>
14. Lee S., Koh J.-H., J. Park.: J. Organomet. Chem. 2001, 637, 99. <https://doi.org/10.1016/S0022-328X(01)00877-4>
15. Muniz-Fernandez K., Bolm C.: Chem. Eur. J. 2000, 6, 2309. <https://doi.org/10.1002/1521-3765(20000703)6:13<2309::AID-CHEM2309>3.0.CO;2-N>