Collect. Czech. Chem. Commun. 2000, 65, 667-672
https://doi.org/10.1135/cccc20000667

A Stereoselective Peptide-Based Artificial Receptor for Sugar Derivatives

Frank Eblinger and Hans-Jörg Schneider*

FR Organische Chemie , Universität des Saarlandes, D 66041 Saarbrücken, Germany

References

1a. Lemieux R. U.: Acc. Chem. Res. 1996, 29, 373. <https://doi.org/10.1021/ar9600087>
1b. Quiocho F. A., Vyas N. K.: Nature 1984, 310, 381. <https://doi.org/10.1038/310381a0>
1c. Quiocho F. A.: Pure Appl. Chem. 1989, 61, 1293. <https://doi.org/10.1351/pac198961071293>
1d. Lee Y. C., Lee R. T.: Acc. Chem. Res. 1995, 8, 321. <https://doi.org/10.1021/ar00056a001>
2. Das G., Hamilton A. D.: J. Am. Chem. Soc. 1994, 116, 11139. <https://doi.org/10.1021/ja00103a032>
3. Coteron J. M., Hacket F., Schneider H.-J.: J. Org. Chem. 1996, 61, 1429. <https://doi.org/10.1021/jo951435l>
4a. Aoyama Y., Tanaka Y.; Sugahara S.: J. Am. Chem. Soc. 1989, 111, 5397. <https://doi.org/10.1021/ja00196a052>
4b. Kurihara K., Ohto K., Tanaka Y., Aoyama Y., Kunitake T.: J. Am. Chem. Soc. 1991, 113, 444. <https://doi.org/10.1021/ja00002a010>
5a. Bhattarai K. M., Bonar-Law R. P., Davis A. P., Murray B. A.: Chem. Commun. 1992, 752.
5b. See also Neidlein U., Diederich F.: Chem. Commun. 1996, 1493. <https://doi.org/10.1039/cc9960001493>
6a. Huang C.-Y., Cabell L. A., Anslyn E. V.: J. Am. Chem. Soc. 1994, 116, 2778. <https://doi.org/10.1021/ja00086a011>
6b. See also Rusin O., Kral V.: Chem. Commun. 1999, 2363.
6c. Staley S. A., Smith B. D.: Tetrahedron Lett. 1996, 37, 283. <https://doi.org/10.1016/0040-4039(95)02150-7>
6d. Mazik M., Bandmann H., Sicking W.: Angew. Chem., Int. Ed. Engl. 2000, 39, 551. <https://doi.org/10.1002/(SICI)1521-3773(20000204)39:3<551::AID-ANIE551>3.0.CO;2-7>
7a. Eliseev A. V., Schneider H.-J.: J. Am. Chem. Soc. 1996, 116, 6081. <https://doi.org/10.1021/ja00093a004>
7b. Hacket F., Schneider H.-J.: Unpublished results.
8. Bonar-Law R. P., Sanders J. K. M.: J. Am. Chem. Soc. 1995, 117, 259. <https://doi.org/10.1021/ja00106a029>
9a. Mizutani T., Kurahashi T., Murakami T., Matsumi N., Ogoshi H.: J. Am. Chem. Soc. 1997, 119, 8991. <https://doi.org/10.1021/ja9713183>
9b. Crossley M. J., Machay L. G., Try A. C.: Chem. Commun. 1995, 1925.
10. Bhattarai K. M., Bonar-Law R. P., Davis A. P., Murray B. A.: Chem. Commun. 1992, 752.
11. Jimenéz-Barbero J., Junquera E., Martin-Pastor M., Sharma S., Vicent C., Penadés S.: J. Am. Chem. Soc. 1995, 117, 1198. <https://doi.org/10.1021/ja00150a016>
12. Inouye M., Miyake T., Furusyo M., Nakazumi H.: J. Am. Chem. Soc. 1995, 117, 12416. <https://doi.org/10.1021/ja00155a006>
13. Cuntze J., Owens L., Alcazar V., Seiler P., Diederich F.: Helv. Chim. Acta 1995, 78, 367. <https://doi.org/10.1002/hlca.19950780209>
14. Greenspoon N., Wachtel E.: J. Am. Chem. Soc. 1991, 113, 7233. <https://doi.org/10.1021/ja00019a021>
15. Liu R., Still W. C.: Tetrahedron Lett. 1993, 34, 2573. <https://doi.org/10.1016/S0040-4039(00)77628-3>
16. James T. D., Sandanayake S., Shinkai S.: Angew. Chem. 1996, 108, 2038; Angew. Chem., Int. Ed. Engl. 1996, 35, 1910. <https://doi.org/10.1002/anie.199619101>
17. Schneider H.-J., Kramer R., Simova S., Schneider U.: J. Am. Chem. Soc. 1988, 110, 6442. <https://doi.org/10.1021/ja00227a025>
18a. Brooks C. L., Karplus M.: Methods Enzymol. 1986, 127, 369. <https://doi.org/10.1016/0076-6879(86)27031-7>
18b. Brünger A. T., Karplus M.: Acc. Chem. Res. 1991, 24, 54. <https://doi.org/10.1021/ar00002a005>
19a. Schneider H.-J., Juneja R. K., Simova S.: Chem. Ber. 1989, 112, 1211. <https://doi.org/10.1002/cber.19891220631>
19b. Sartorius J., Schneider H.-J.: Chem. Eur. J. 1996, 2, 1446. <https://doi.org/10.1002/chem.19960021118>
20. Greenstein J. P., Winitz M.: Chemistry of the Amino Acids. John Wiley and Sons, Inc., New York–London 1961.