Domino syntheses of five-, six- and seven-membered O-, N- and S-heterocycles from α-, β- and γ-substituted carboxylic esters

Journal of the Chemical Society - Perkin Transactions 1

Volumn , Issue 23, 1996, Pages 2799-2802

  Loffler J ^a   Schobert, R ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33748956846     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/P19960002799     Document Type: Article

References (30)

1. R. Schobert, S. Müller and H. J. Bestmann, Synlett, 1995, 425.
2. (a) N. Hirayama, M. Kasai, K. Shirahata, Y. Kashi and Y. Sasada, Tetrahedron Lett., 1980, 2559;
3. (b) T. P. C. Mulholland, R. Foster and D. B. J. Haydock, J. Chem. Soc., Perkin Trans. 1, 1972, 1225;
4. (c) P. J. Jerris, P. M. Wovkulich and A. B. Smith, Tetrahedron Lett., 1979, 47, 4517;
5. (d) S. Gelin and P. Pollet, Synth. Commun., 1980, 10, 11.
6. Y. Miki, H. Kinoshita, T. Yoshimaru and S. Takemura, Heterocycles, 1987, 26, 199.
7. (a) H. J. Bestmann and R. Schobert, Synthesis, 1989, 419;
8. (b) H. J. Bestmann and D. Sandmeier, Angew. Chem., 1975, 87, 630;
9. Angew. Chem., Int. Ed. Engl., 1975, 14, 634;
10. Chem. Ber., 1980, 113, 274.
11. (a) H. J. Bestmann, M. Schmidt and R. Schobert, Synthesis, 1988, 49;
12. (b) J. Brennan and P. J. Murphy, Tetrahedron Lett., 1988, 29, 2063.
13. (a) M. Tsunakawa and S. Toda, J. Antibiot., 1980, 33, 166;
14. (b) R. C. F. Jones and J. M. Patience, J. Chem. Soc., Perkin Trans. 1, 1990, 8, 2350.
15. (a) S. Omura, A. Nakagawa, R. Iwata and A. Hatano, J. Antibiot., 1983, 36, 1781;
16. (b) C. L. Wang and J. M. Salvino, Tetrahedron Lett., 1984, 25, 5243;
17. (c) C. Corral and J. Lissavetzky, J. Chem. Soc., Perkin Trans. 1, 1984, 12, 2711.
18. (a) E. Winterfeldt, J. Heterocycl. Chem., 1992, 29, 631;
19. (b) A. Kruger, J. S. Afr. Chem. Inst., 1973, 26, 132.
20. (a) P. Da Re and E. Sandri, Chem. Ber., 1960, 93, 1085;
21. (b) H. J. Bestmann and H. J. Lang, Tetrahedron Lett., 1969, 25, 2100;
22. (c) E. Ziegler and H. Junek, Monatsh. Chem., 1955, 86, 29;
23. (d ) I. Heilbron and D. Hill, J. Chem. Soc., 1927, 2, 705.
24. (a) J. R. Price, Fortschr. Chem. Org. Naturst., 1956, 13, 302;
25. (b) H. Matthes and E. Schreiber, Ber. Dtsch. Pharm. Ges., 1914, 24, 385;
26. (c) G. M. Coppola, G. E. Hardtmann and O. R. Pfister, J. Org. Chem., 1976, 41, 825.
27. (a) N. Hiroyuki, E. Takashi, N. Toshiuki and K. Teijiro, J. Heterocycl. Chem., 1985, 22, 89;
28. (b) N. Hiroyuki, K. Yuzoh and K. Teijiro, J. Heterocycl. Chem. 1992, 29, 135.
29. F. Bohlmann, C. Zdero and H. Franke, Chem. Ber., 1973, 106, 382.
30. B. Neises and W. Steglich, Org. Synth., 1984, 63, 183.