Total synthesis of (-)- and ent-(+)-4-desacetoxy-5-desethylvindoline

Heterocycles

Volumn 72, Issue , 2007, Pages 95-102

  Ishikawa, Hayato ^a   Boger, Dale L ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 34547830832     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-06-s(k)8     Document Type: Article

References (25)

1. Norbert N., and Neuss M.N. In: Brossi A., and Suffness M. (Eds). The Alkaloids Vol. 37 (1990), Academic, San Diego 229-240
2. Noble R.L., Beer C.T., and Cutts J.H. Ann. N. Y. Acad. Sci. 76 (1958) 882
3. Noble R.L. Lloydia 27 (1964) 280
4. Svoboda G.H., Neuss N., and Gorman M. J. Am. Pharm. Assoc. Sci. Ed. 48 (1959) 659
5. Owellen R.J., Hartke C.A., Dickerson R.M., and Hains F.O. Cancer Res. 36 (1976) 1499
6. Pearce H.L. In: Brossi A., and Suffness M. (Eds). The Alkaloids Vol. 37 (1990), Academic, San Diego 145
7. Ishikawa H., Elliott G.I., Velcicky J., Choi Y., and Boger D.L. J. Am. Chem. Soc. 128 (2006) 10596
8. Choi Y., Ishikawa H., Velcicky J., Elliott G.I., Miller M.M., and Boger D.L. Org. Lett. 7 (2005) 4539
9. Elliott G.I., Velcicky J., Ishikawa H., Li Y., and Boger D.L. Angew. Chem. Int. Ed. 45 (2006) 620
10. Yuan Z.-Q., Ishikawa H., and Boger D.L. Org. Lett. 7 (2005) 741
11. Neuss N., Barnes A.J., and Huckstep L.L. Experientia 31 (1975) 18
12. Barnett C.J., Cullinan G.J., Gerzon K., Hoying R.C., Jones W.E., Nevlon W.M., Poore G.A., Robison R.L., Sweeney M.J., Todd G.C., Dyke R.W., and Nelson R.L. J. Med. Chem. 21 (1978) 88
13. Gigant B., Wang C., Ravelli R.B.G., Roussi F., Steinmetz M.O., Curmi P.A., Sobel A., and Knossow M. Nature 435 (2005) 519
14. Elliott G.I., Fuchs J.R., Blagg B.S.J., Ishikawa H., Tao H., Yuan Z.-Q., and Boger D.L. J. Am. Chem. Soc. 128 (2006) 10589
15. Wilkie G.D., Elliott G.I., Blagg B.S.J., Wolkenberg S.E., Soenen D.R., Miller M.M., Pollack S., and Boger D.L. J. Am. Chem. Soc. 124 (2002) 11292
16. Wolkenberg S.E., and Boger D.L. J. Org. Chem. 67 (2002) 7361
17. Christl M., Lanzendoerfer U., Groetsch M.M., Ditterich E., and Hegmann J. Chem. Ber. 123 (1990) 2031
18. The X-ray crystal structure of 15 (CCDC 609613) has been deposited with the Cambridge Crystallographic Data Centre.
19. Lawesson S.O., and Pedersen B.S. Tetrahedron 35 (1979) 2433
20. Kuehne M.E., Okuniewicz F.J., Kirkemo C.L., and Bohnert J.C. J. Org. Chem. 47 (1982) 1335
21. Kuehne M.E., and Podhorez D.E. J. Org. Chem. 50 (1985) 924
22. Kobayashi S., Ueda T., and Fukuyama T. Synlett (2000) 883
23. Iimori T., Ohtsuka Y., and Oishi T. Tetrahedron Lett. 32 (1991) 1209
24. Mitsunobu O. Synthesis (1981) 1
25. 3).