Pure Appl. Chem., 2007, Vol. 79, No. 4, pp. 677-684
http://dx.doi.org/10.1351/pac200779040677
Synthesis of an analog of mycothiazole and total synthesis of pseudotrienic acid B
References
- 1. P. Crews, Y. Kakou, E. Quinoa. J. Am. Chem. Soc. 110, 4365 (1988). (http://dx.doi.org/10.1021/ja00221a042)
- 2. A. Cutignano, I. Bruno, G. Bifulco, A. Casapullo, C. Debitus, L. Gomez-Paloma, R. Riccio. Eur. J. Org. Chem. 775 (2001). (http://dx.doi.org/10.1002/1099-0690(200102)2001:4<775::AID-EJOC775>3.0.CO;2-Z)
- 3. The results of the National Cancer Institute Human Tumor Cell Line Screen mean graph can be consulted on the Internet at <http://www.dtp.nci.nih.gov> (NCS number 647640).
- 4. R. N. Sonnenschein, T. A. Johnson, K. Tenney, F. A. Valeriote, P. Crews. J. Nat. Prod. 69, 145 (2006). (http://dx.doi.org/10.1021/np0503597)
- 5. (a). H. Sugiyama, F. Yokokawa, T. Shioiri. Org. Lett. 2, 2149 (2000); (http://dx.doi.org/10.1021/ol000128l)
- 5. (b). H. Sugiyama, F.Yokokawa, T. Shioiri. Tetrahedron 59, 6579 (2003). (http://dx.doi.org/10.1016/S0040-4020(03)01020-2)
- 6. M. Scholl, S. Ding, C. W. Lee, R. H. Grubbs. Org. Lett. 1, 953 (1999). (http://dx.doi.org/10.1021/ol990909q)
- 7. S. Karsch, P. Schwab, P. Metz. Synlett 2019 (2002).
- 8. A. Le Flohic, C. Meyer, J. Cossy, J.-C. Galland, J.-R. Desmurs. Synlett 667 (2003).
- 9. A. Le Flohic, C. Meyer, J. Cossy. Org. Lett. 7, 339 (2005). (http://dx.doi.org/10.1021/ol047603q)
- 10. A. Le Flohic, C. Meyer, J. Cossy. Tetrahedron 62, 9017 (2006). (http://dx.doi.org/10.1016/j.tet.2006.07.010)
- 11. (a). B. Plietker, P. Metz. Tetrahedron Lett. 39, 7827 (1998); (http://dx.doi.org/10.1016/S0040-4039(98)01743-2)
- 11. (b). B. Plietker, D. Seng, R. Frohlich, P. Metz. Eur. J. Org. Chem. 3669 (2001). (http://dx.doi.org/10.1002/1099-0690(200110)2001:19<3669::AID-EJOC3669>3.0.CO;2-S)
- 12. A. Pohanka, A. Broberg, M. Johansson, L. Kenne, J. Levenfors. J. Nat. Prod. 68, 1380 (2005). (http://dx.doi.org/10.1021/np050243a)
- 13. J. S. Kingsbury, J. P. A. Harrity, P. J. Bonitatebus Jr., A. H. Hoveyda. J. Am. Chem. Soc. 121, 791 (1999). (http://dx.doi.org/10.1021/ja983222u)
- 14. A. Hafner, R. O. Duthaler, R. Marti, J. Rihs, P. Rhote-Streit, F. Schwarzenbach. J. Am. Chem. Soc. 114, 2321 (1992). (http://dx.doi.org/10.1021/ja00033a005)
- 15. The 2R,3R absolute configuration of 13 was confirmed by the 1H NMR spectra of the two corresponding mandelates, according to the procedure described in J. M. Seco, E. Quinoa, R. Riguera. Tetrahedron: Asymmetry 12, 2915 (2001).
- 16. P. H. J. Carlsen, T. Katsuki, V. S. Martin, K. B. Sharpless. J. Org. Chem. 46, 3936 (1981). (http://dx.doi.org/10.1021/jo00332a045)
- 17. B. H. Lipshutz, E. L. Ellworth, S. H. Dimock, D. C. Reuter. Tetrahedron Lett. 30, 2065 (1989). (http://dx.doi.org/10.1016/S0040-4039(01)93712-8)
- 18. D. Amans, V. Bellosta, J. Cossy. Angew. Chem., Int. Ed. 45, 5870 (2006). (http://dx.doi.org/10.1002/anie.200601114)