Collect. Czech. Chem. Commun. 2000, 65, 816-828
https://doi.org/10.1135/cccc20000816

Stereoselective Synthesis of 2-Substituted Pyrrolidines

Sandrine Deloisya, Heiko Tietgenb and Horst Kunzb,*

a Université de Paris-Sud, ICMO, Laboratoire des Carbocycles, F-91405 Orsay cedex, France
b Institut für Organische Chemie, Universität Mainz, D-55099 Mainz, Germany

References

1a. For reviews, see: Silvermann R. B.: The Organic Chemistry of Drug Design and Drug Action. Academic Press, San Diego 1992.
1b. Laschat S.: Liebigs Ann. Chem. 1997, 1. <https://doi.org/10.1002/jlac.199719970104>
2. Mothes K., Schütte H. R., Luckner M.: Biochemistry of Alkaloids. VCH, Weinheim 1985.
3a. For review, see: Winchester B., Fleet G. W.: Glycobiology 1992, 2, 199. <https://doi.org/10.1093/glycob/2.3.199>
3b. Bringmann G., Götz R., Harmsen S., Holenz J., Walter R.: Liebigs Ann. Chem. 1996, 2045. <https://doi.org/10.1002/jlac.199619961215>
4. Tramer D., Porth S., Opatz T., Bats J. W., Giester G., Mulzer J.: Synthesis 1988, 653.
5. Kuguchi T., Nakazono Y., Kotera S., Ninomya I., Naito T.: Heterocycles 1991, 1525.
6. Husson H.-P., Royer J.: Chem. Soc. Rev. 1999, 28, 383. <https://doi.org/10.1039/a900153k>
7. Oppolzer W., Bochet C. G., Merifield E.: Tetrahedron Lett. 1994, 35, 7015. <https://doi.org/10.1016/0040-4039(94)88213-4>
8. Enders D., Trebes J.: Liebigs Ann. Chem. 1993, 1941.
9. Review: Arend M., Westermann B., Risch N.: Angew. Chem. 1998, 110, 1096; Angew. Chem., Int. Ed. Engl. 1998, 37, 1044. <https://doi.org/10.1002/(SICI)1521-3773(19980504)37:8<1044::AID-ANIE1044>3.0.CO;2-E>
10. Review: Kunz H., Weymann M., Follmann M., Allef P., Oertel K., Schultz-Kukula M., Hofmeister A.: Polish J. Chem. 1999, 73, 15.
11. Kunz H., Pfrengle W.: Angew. Chem. 1989, 101, 1041; Angew. Chem., Int. Ed. Engl. 1989, 28, 1067. <https://doi.org/10.1002/anie.198910671>
12. Weymann M., Pfrengle W., Schollmeyer D., Kunz H.: Synthesis 1997, 1151. <https://doi.org/10.1055/s-1997-3185>
13a. Laschat S., Kunz H.: Synlett 1990, 51. <https://doi.org/10.1055/s-1990-20985>
13b. Laschat S., Kunz H.: Synlett 1990, 629. <https://doi.org/10.1055/s-1990-21192>
14. Deloisy S., Kunz H.: Tetrahedron Lett. 1998, 39, 791. <https://doi.org/10.1016/S0040-4039(97)10720-1>
15. Kunz H., Pfrengle W., Sager W.: Tetrahedron Lett. 1989, 30, 4109. <https://doi.org/10.1016/S0040-4039(00)99334-1>
16. Cooper J. L., Harding K. E.: Tetrahedron Lett. 1977, 18, 3321. <https://doi.org/10.1016/S0040-4039(01)83229-9>
17. Julia M., Fournerou J.-D.: Tetrahedron 1976, 32, 113. <https://doi.org/10.1016/0040-4020(76)85034-X>
18. Burgess L. E., Meyers A. I.: J. Org. Chem. 1992, 57, 1656. <https://doi.org/10.1021/jo00032a012>
19. Seeman J. I., Chavdarian G. G., Secor H. V.: J. Org. Chem. 1985, 50, 5419. <https://doi.org/10.1021/jo00225a094>
20. Kunz H., Sager W., Schanzenbach D., Decker M.: Liebigs Ann. Chem. 1991, 649. <https://doi.org/10.1002/jlac.1991199101117>
21. Kunz H., Pfrengle W., Rück K., Sager W.: Synthesis 1991, 1039. <https://doi.org/10.1055/s-1991-26641>
22. Laschat S., Kunz H.: J. Org. Chem. 1991, 56, 5883. <https://doi.org/10.1021/jo00020a033>