Intramolecular Heck reaction for the synthesis of isochromanes under ambient and high pressure

Liebigs Annales

Volumn , Issue 5, 1997, Pages 887-891

  Tietze, Lutz F ^a   Burkhardt, Olaf ^a   Henrich, Marielouise ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

Heck reaction, intramolecular; Heterocycles; High pressure chemistry; Isochromane; Palladium

Indexed keywords

EID: 0038621234     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719970516     Document Type: Article

References (38)

1. [1a] L. F Tietze, Chem. Rev. 1996, 96, 115-136.
2. [1b] L. F. Tietze, U. Beifuss, Angew. Chem. 1993, 705, 137-170;
3. Angew. Chem. Int. Ed. Engl. 1993, 52, 131.
4. [2a] E. Negishi, C. Coperet, Chem. Rev. 1996, 96, 365.
5. [2b] W. Cabri, I. Candiani, Acc. Chem. Res. 1995, 28, 2.
6. [2c] A. de Meijcre, F. E. Meyer, Angew. Chem. 1994, 106, 2473;
7. Angew. Chem. Int. Ed Engl. 1994, 33, 2379.
8. [2d] R. F. Heck in Comprehensive Organic Synthesis, Vol. 4 (Ed.: B. M. Trost, I. Fleming), Pergamon Press, Oxford, 1991, p. 833.
9. [12e] G. D. Daves, A. Hallberg, Chem. Rev. 1989, 89, 1433.
10. [2f] H. J. Altenbach, Nachr. Chem. Tech. Lab. 1988, 36, 1324.
11. [2g] H. U. Reissig, Nachr. Chem. Tech. Lab. 1986, 34, 1066.
12. [2h] R. F. Heck, Palladium Reagents in Organic Syntheses, Academic Press, London, 1985.
13. [2i] L. F. Tietze, Th. Nöbel, Angew. Chem. 1996, 108, 2385-2368;
14. Angew. Chem. Int. Ed. Engl. 1996, 35, 2259-2261.
15. [3a] K. Kondo, M. Sodeoka, M. Mori, M. Shibasaki, Synthesis 1993, 920-930.
16. [3b] A. Ashimori, L. E. Overman, J. Org. Chem. 1992, 57, 4823-4832.
17. [3c] H.-G. Schmalz, Nachr. Chem. Tech. Lab. 1994, 42 (3), 270-276.
18. [3d] Y. Koga, M. Sodeoka, M. Shibasaki, Tetrahedron Lett. 1994, 55, 1227-1230.
19. [3e] L. F. Tietze, T. Grote, J. Org. Chem. 1994, 59, 192-196.
20. [3f] J. J. Masters, D. K. Jung, W. G. Bornmann, S. J. Danishefsky, Tetrahedron Lett. 1993, 34, 7253-7256.
21. [3g] G. Balme, D. Bouyssi, Tetrahedron, 1994, 50, 403-414.
22. [4a] L. F. Tietze, R. Schimpf, Synthesis 1993, 876-330.
23. [4b] L. F. Tietze, R. Schimpf, Chem. Ber. 1994, 127, 2235-2240.
24. [4c] L. F. Tietze, R. Schimpf, Angew. Chem. 1994, 106, 1138-1139;
25. Angew. Chem. Int. Ed. Engl. 1994, 55, 1089-1090.
26. [4d] L. F. Tietze, T. Raschke, Synlett 1995, 597.
27. [4e] L. F. Tietze, T. Raschke, Liebigs Ann. 1996 1981-1987.
28. [4f] L. F. Tietze, K. H. Heitmann, T. Raschke, Synlett 1997, 35-37.
29. [5a] L. F. Tietze, O. Burkhardt, Synthesis 1994, 1331.
30. [15b] L. F. Tietze, O. Burkhardt, Liebigs Ann. 1995, 1153.
31. [6a] T. Eicher, S. Hauptmann, Chemie der Heterocyclen, Thieme-Verlag, Stuttgart, 1994, p. 269.
32. [6b] L. F. Tietze, J. Görlitzer, Synlett 1996, 11, 1041.
33. [7a] E. A. Markaryan, A. G. Samodurova, Russ. Chem. Rev. 1989, 58, 479.
34. [7b] Y. C. Xu, E. Lebeau, J. W. Gillard, G. Attardo, Tetrahedron Lett. 1993, 34, 3841.
35. [7c] M. P. DeNinno, R. J. Perner, H. E. Morton, S. DiDomenico, Jr., J. Org. Chem. 1992, 57, 7115.
36. [8a] M. Yamamoto, K. Hashigaki, K. Hiromatsu, K. Tasaka, Chem. Pharm. Bull. 1983, 31, 521.
37. [8b] Japanese patent 76-138680; Chem. Abstr. 1977, 87, 23046.
38. L. F. Tietze, O. Burkhardt, unpublished results.