Collect. Czech. Chem. Commun.
2000, 65, 83-98
https://doi.org/10.1135/cccc20000083
Synthesis of 2,2'-Bipyridines with Axially Chiral 1,1'-Binaphthalene Units
Jana Hodačováa,* and Ivan Stiborb
a Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 166 10 Prague 6, Czech Republic
b Department of Organic Chemistry, Prague Institute of Chemical Technology, 166 28 Prague 6, Czech Republic
References
1a. Vögtle F.: Supramolekulare Chemie. Teubner, Stuttgart 1989.
1b. Lhoták P., Stibor I.: Molekulární design. VŠCHT, Praha 1997.
2a. Lehn J.-M.: Supramolecular Chemistry: Concepts and Perspectives. VCH, Weinheim 1995.
2b. Constable E. in: Comprehensive Supramolecular Chemistry (J. L. Atwood, J. E. D. Davies, D. D. MacNicol and F. Vögtle, Eds), Vol. 9, p. 213. Elsevier, Oxford 1996.
2c. Chem. Rev. 1997, 97, 2005.
< C., Bernardinelli G., Hopfgartner G.: https://doi.org/10.1021/cr960053s>
3a. Chem. Rev. 1998, 98, 2405.
< L.: https://doi.org/10.1021/cr970463w>
3b. Eliel E. L., Wilen S. H., Mander L. N.: Stereochemistry of Organic Compounds. Wiley, New York 1994.
3c. Takaya H., Ohta T., Noyori R. in: Catalytic Asymmetric Synthesis (I. Ojima, Ed.), p. 1. VCH, New York 1993.
4a. J. Organomet. Chem. 1989, 379, 17.
< C., Schionato A., Chelluci G., Brunner H., Kürzinger A., Obermann U.: https://doi.org/10.1016/0022-328X(89)87271-7>
4b. Tetrahedron: Asymmetry 1993, 4, 143.
< H., Yamaguchi S., Park S.-B., Itoh K.: https://doi.org/10.1016/S0957-4166(00)86024-3>
5a. Angew. Chem., Int. Ed. Engl. 1990, 29, 205.
< C., Zehnder M., Bur D.: https://doi.org/10.1002/anie.199002051>
5b. Chem. Ber. 1992, 125, 1169.
< C., Ewald M., Felder M., Schlingloff G.: https://doi.org/10.1002/cber.19921250528>
6a. Synlett 1992, 575.
< K., Tabuchi S., Katsuki T.: https://doi.org/10.1055/s-1992-21420>
6b. Tetrahedron Lett. 1993, 34, 2661.
< K., Katsuki T.: https://doi.org/10.1016/S0040-4039(00)77650-7>
6c. J. Chem. Soc., Dalton Trans. 1998, 1043.
< H.-L., Lee W.-S., Ng H.-F., Chiu W.-H., Wong W.-T.: https://doi.org/10.1039/a706754b>
7. Tetrahedron: Asymmetry 1998, 9, 531.
< G., Pinna G. A., Saba A.: https://doi.org/10.1016/S0957-4166(97)00624-1>
8. Helv. Chim. Acta 1984, 67, 2264.
< J.-C., Alpha B., Plancherel D., Lehn J.-M.: https://doi.org/10.1002/hlca.19840670833>
9. Helv. Chim. Acta 1988, 71, 1042.
< B., Anklam E., Deschenaux R., Lehn J.-M., Pietraskiewicz M.: https://doi.org/10.1002/hlca.19880710515>
10. J. Chem. Soc. 1938, 1662.
< F. H.: https://doi.org/10.1039/jr9380001662>
11a. Synth. Commun. 1992, 22, 1033.
< J. P., Topgi R. S., Kelly J. W.: https://doi.org/10.1080/00397919208019294>
11b. J. Am. Chem. Soc. 1995, 117, 2533.
< J. P., Kelly J. W.: https://doi.org/10.1021/ja00114a016>
12. Ber. Dtsch. Chem. Ges. 1926, 59, 2159.
< R., Prell E., Rieche A.: https://doi.org/10.1002/cber.19260590881>
13a. Angew. Chem., Int. Ed. Engl. 1993, 32, 1147.
< K., Okada T., Toda F.: https://doi.org/10.1002/anie.199311471>
13b. Org. Synth. 1998, 75, 1.
D., Hughes D. L., Verhoeven T. R., Reider P. J.:
13c. J. Org. Chem. 1988, 53, 3607.
< F., Tanaka K.: https://doi.org/10.1021/jo00250a037>
13d. Org. Synth. 1989, 67, 1.
J., Fouquey C.:
13e. Org. Synth. 1989, 67, 13.
L. K.:
13f. J. Org. Chem. 1977, 42, 4173.
< E. P., Gokel G. W., Jong F. de, Koga K., Sousa L. R., Siegel M. G., Kaplan L., Sogah G. D. Y., Cram D. J.: https://doi.org/10.1021/jo00862a001>
13g. Org. Synth. 1992, 70, 60.
R. J.:
13h. Synthesis 1990, 222.
< Y., Heung-Cho P., Iizuka K., Okamura A., Miyano S.: https://doi.org/10.1055/s-1990-26838>
13i. J. Org. Chem. 1993, 58, 7313.
< J.-M., Buono G.: https://doi.org/10.1021/jo00077a072>
13j. Tetrahedron: Asymmetry 1995, 6, 111.
< Z., Zamojski A.: https://doi.org/10.1016/0957-4166(94)00365-I>
13k. Tetrahedron: Asymmetry 1995, 6, 341.
< M., Prasad A. S. B., Kanth J. V. B., Reddy C. K.: https://doi.org/10.1016/0957-4166(95)00008-D>
14. Tetrahedron Lett. 1992, 33, 2253.
< P. J., Wang W., Snieckus V.: https://doi.org/10.1016/S0040-4039(00)74182-7>
15. Org. Prep. Proced. Int. 1995, 27, 685.
< J., Li W., Li Y., Li Y., Yang S.: https://doi.org/10.1080/00304949509458533>
16a. Chem. Eur. J. 1997, 3, 969.
< P., Beaujolais V., Gaude D., Coulombeau C., Pierre J.-L.: https://doi.org/10.1002/chem.19970030619>
16b. Collect. Czech. Chem. Commun. 1997, 62, 925.
< V., Stibor I.: https://doi.org/10.1135/cccc19970925>
17. J. Org. Chem. 1978, 43, 1930.
< D., Helgeson R. C., Peacock S. C., Kaplan L. J., Domeier L. A., Moreau P., Koga K., Mayer J. M., Chao Y., Siegel M. G., Hoffman D. H., Sogah G. D. Y.: https://doi.org/10.1021/jo00404a019>
18. Org. Prep. Proced. Int. 1991, 23, 200.
< M., Závada J.: https://doi.org/10.1080/00304949109458313>
19. Bull. Soc. Chim. Fr. 1988, 6, 995.
W., Baret P., Pierre J.-L.:
20. Tetrahedron 1971, 27, 5999.
< H., Yamada S.: https://doi.org/10.1016/S0040-4020(01)91765-X>
21. J. Org. Chem. 1996, 61, 3093.
< H. T., Kellogg R. M.: https://doi.org/10.1021/jo952107o>
22. Z. Kristallogr., New Cryst. Struct. 1997, 212, 461.
S., Ondráček J., Hodačová J., Stibor I.:
23a. Proc. Natl. Acad. Sci. U.S.A. 1987, 84, 2565.
< J.-M., Rigault A., Siegel J., Harrowfield J., Chevrier B., Moras D.: https://doi.org/10.1073/pnas.84.9.2565>
23b. Angew. Chem., Int. Ed. Engl. 1988, 27, 1095.
< J.-M., Rigault A.: https://doi.org/10.1002/anie.198810951>
23c. Helv. Chim. Acta 1991, 74, 1843.
< W., Hall J., Lehn J.-M., Bolm C.: https://doi.org/10.1002/hlca.19910740827>
23d. Angew. Chem., Int. Ed. Engl. 1996, 35, 1830.
< C. R., Benaglia M., Cozzi F., Siegel J. S.: https://doi.org/10.1002/anie.199618301>
24. J. Am. Chem. Soc. 1980, 102, 2043.
< S. S., Walba D. M., Garta F. C. A., Helgeson R. C., Cram D. J.: https://doi.org/10.1021/ja00526a046>
25. Bull. Chem. Soc. Jpn. 1997, 70, 207.
< H., Ito K., Aoki Y., Katsuki T.: https://doi.org/10.1246/bcsj.70.207>
26. J. Org. Chem. 1981, 46, 393.
< D. S., Helgeson R. O., Cram D. J.: https://doi.org/10.1021/jo00315a033>
27. J. Org. Chem. 1991, 56, 2096.
< G., Spada G. P.: https://doi.org/10.1021/jo00006a025>
28. Tetrahedron 1992, 48, 9503.
< M., Ščigel R., Günterová J., Tichý M., Závada J.: https://doi.org/10.1016/S0040-4020(01)88318-6>
29. J. Org. Chem. 1979, 44, 2538.
< R. C., Tarnowski T. L., Cram D. J.: https://doi.org/10.1021/jo01328a045>