Pure and Applied Chemistry

Pure Appl. Chem., 2011, Vol. 83, No. 3, pp. 699-707

http://dx.doi.org/10.1351/PAC-CON-10-08-15

Published online 2011-01-31

Selective transformations of cephalostatin analogues

References

• 1. NCI-60 data are available on the web at <http://dtp.nci.nih.gov>. Cephalostatin 1 has the code NSC-363979.
• 2a. G. R. Pettit, Z. A. Cichacz, F. Gao, C. L. Herald, M. R. Boyd, J. M. Schmidt, J. N. A. Hooper. J. Org. Chem. 58, 1302 (1993). (http://dx.doi.org/10.1021/jo00058a004)
• 2b. G. R. Pettit, Z. A. Cichacz, F. Gao, C. L. Herald, M. R. Boyd. J. Chem. Soc., Chem. Commun. 1166 (1993). (http://dx.doi.org/10.1039/c39930001166)
• 2c. G. R. Pettit, C. L. Herald, Z. A. Cichacz, F. Gao, M. R. Boyd, N. D. Christie, J. M. Schmidt. Nat. Prod. Lett. 3, 239 (1993).
• 3. A. Kramer, U. Ullmann, E. Winterfeldt. J. Chem. Soc., Perkin Trans. 1 2865 (1993). (http://dx.doi.org/10.1039/p19930002865)
• 4. C. H. Heathcock, S. C. Smith. J. Org. Chem. 59, 6828 (1994). (http://dx.doi.org/10.1021/jo00101a052)
• 5a. M. Droegemueller, T. Flessner, R. Jautelat, U. Scholz, E. Winterfeldt. Eur. J. Org. Chem. 2811 (1998).
• 5b. T. Flessner, R. Jautelat, U. Scholz, E. Winterfeldt. Forschr. Chem. Org. Naturst. 87, 1 (2004) and all refs. therein.
• 6. T. G. LaCour, C. Guo, S. Bhandaru, M. R. Boyd, P. L. Fuchs. J. Am. Chem. Soc. 120, 692 (1998). (http://dx.doi.org/10.1021/ja972160p)
• 7. J. U. Jeong, C. Guo, P. L. Fuchs. J. Am. Chem. Soc. 121, 2071 (1999). (http://dx.doi.org/10.1021/ja9817141)
• 8. S. Kim, S. C. Sutton, C. Guo, T. G. LaCour, P. L. Fuchs. J. Am. Chem. Soc. 121, 2056 (1999). (http://dx.doi.org/10.1021/ja9817139)
• 9. K. C. Fortner, D. Kato, Y. Tanaka, M. D. Shair. J. Am. Chem. Soc. 132, 275 (2010). (http://dx.doi.org/10.1021/ja906996c)
• 10. S. Bäsler, A. Brunck, R. Jautelat, E. Winterfeldt. Helv. Chim. Acta 83, 1854 (2000). (http://dx.doi.org/10.1002/1522-2675(20000809)83:8<1854::AID-HLCA1854>3.0.CO;2-4)
• 11. T. G. LaCour, P. L. Fuchs. Tetrahedron Lett. 40, 4655 (1999). (http://dx.doi.org/10.1016/S0040-4039(99)00827-8)
• 12. M. Nawasreh. Bioorg. Med. Chem. 16, 255 (2008). (http://dx.doi.org/10.1016/j.bmc.2007.09.043)
• 13. M. Nawasreh, E. Winterfeldt. Curr. Org. Chem. 7, 649 (2003). (http://dx.doi.org/10.2174/1385272033486774)
• 14. M. Nawasreh. Nat. Prod. Res. 21, 1 (2007).
• 15. M. Nawasreh. Chin. Chem. Lett. 19, 1391 (2008). (http://dx.doi.org/10.1016/j.cclet.2008.09.055)