Polyene Cyclization to Adociasulfate 1

Organic Synthesis Set

Volumn , Issue , 2008, Pages 342-349

  Lindel, Thomas ^a,b   Hopmann, Cordula ^c  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c NONE

Author keywords

Adociasulfate; Desilylation; Hydroquinone; Microtubule; Polyprenoids

Indexed keywords

EID: 84889618371     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527620784.ch31d     Document Type: Chapter

References (33)

1. Reviews: a) J. K. SUTHERLAND in Comprehensive Organic Synthesis, Vol. 3 (Eds.: B. M. TROST, I. FLEMING), Pergamon Press, Oxford, 1991, 341-377.
2. L. F. Tietze, U. Beifuss, Angew. Chem 1993, 205, 137-170.
3. Angew. Chem. Int. Ed. Engl. 1993, 32, 131-63.
4. W. S. Johnson, M. B. Gravestock, B. E. Mccarhy, J. Am. Chem. Soc 1971, 93, 4332-4334.
5. W. S. Johnson, Angew. Chem 1976, 88, 33-41.
6. Angew. Chem. Int. Ed. Engl. 1976, 25, 9-17.
7. M. Bogenstatter, A. Llmberg, L. E. Overman, et al., J. Am. Chem. Soc. 1999, 121, 12, 206-12, 207.
8. R. Sakowicz, M. S. Berdelis, K. Ray, et al., Science 1998, 280, 292-295.
9. C. L. Blackburn, C. Hopmann, R. Sakowicz, et al., y. Org. Chem 1999, 64, 5565-5570.
10. J. A. Kalaitzis, P. De Almeida Leone, L. Harris, et al., J. Org. Chem 1999, 53, 5571-5574.
11. J. A. Kalaitzis, R. J. Quinn, J. Nat. Prod 1999, 62, 1682-1684.
12. C. L. Blackburn, D. J. Faulkner, Tetrahedron 2000, 56, 8429-8432.
13. L. S. B. Goldstein, Trends Cell Biol 2001, 11, 477-482.
14. R. L. Karcher, S. W. Deacon, V. I. Gelfand, Trends Cell Biol 2002, 12, 21-27.
15. A. Holzinger, U. Lutz-Meindl, Cell. Biol. Intern. 2002, 26, 689-697.
16. R. J. Stewart, J. P. Thaler, L. S. B. Goldstein, Proc. Natl. Acad. Sci. USA 1993, 99, 5209-5213.
17. E. J. Corey, G. Luo, L. S. Lin, J. Am. Chem. Soc 1997, 119, 9927-9928.
18. E. J. Corey, G. Luo, L. S. Lin, Angew. Chem 1998, 110, 1147-1148.
19. Angew. Chem. Int. Ed. Engl. 1998, 37, 1126-1128.
20. J. Burfeindt, M. Patz, M. Müller, et al., J. Am. Chem. Soc. 1998, 220, 3629-3634.
21. M. Mohri, H. Kinoshita, K. Inomata, et al., Chem. Lett. 1985, 451-454.
22. J. M. Saa, M. Dopico, G. Martorell, et al.J. Org. Chem. 1998, 55, 991-995.
23. K. Mori, M. Amaike, M. Itou, Tetrahedron 1993, 49, 1871-1878.
24. D. H. R. Barton, J. Dorchak, J. Jaszberenyi, Tetrahedron 1992, 48, 7435-7446.
25. S. Isaacs, A. Hizi, Y. Kashman, Tetrahedron 1993, 49, 4275-4282.
26. A. Rueda, E. Zußia, M. Ortega, et al., J. Org. Chem. 1997, 62, 1481-1485.
27. D. H. R. Barton, S. W. Mccombie, J. Chem. Soc, Perkin Trans. 1 1975, 1574.
28. J. E. Mcmurry, W. J. Scott, Tetrahedron Lett. 1983, 24, 979.
29. P. Schaeffer, J. Poinsot, V. Hauke, et al., Angew. Chem 1994, 106, 1235-1238.
30. Angew. Chem. Int. Ed. Engl. 1994, 33, 1166-1169.
31. W. W. Harding, P. A. Lewis, H. Jacobs, et al., Tetrahedron Lett. 1995, 36, 9137-9140.
32. Z. Xiong, E. J. Corey, J. Am. Chem. Soc. 2000, 222, 4831-4832.
33. Z.-X. Wang, Y. Tu, M. Frohn, et al., J. Am. Chem. Soc. 1997, 229, 11, 224-11, 235.