Pure Appl. Chem., 2008, Vol. 80, No. 5, pp. 1141-1148
http://dx.doi.org/10.1351/pac200880051141
Toward the total synthesis of ritterazine N
References
- 1. S. Fukuzawa, S. Matsunaga, N. Fusetani. J. Org. Chem. 62, 4484 (1997). (http://dx.doi.org/10.1021/jo970091r)
- 2. (a). J. S. Lee, P. L. Fuchs J. Am. Chem. Soc. 127, 13122 (2005); (http://dx.doi.org/10.1021/ja0531935)
- 2. (b). M. Nawasreh, E. Winterfeldt. Curr. Org. Chem. 7, 649 (2003). (http://dx.doi.org/10.2174/1385272033486774)
- 3. (a). D. F. Taber, K. V. Taluskie. J. Org. Chem. 71, 2797 (2006); (http://dx.doi.org/10.1021/jo052656m)
- 3. (b). D. F. Taber, J.-M. Joerger. J. Org. Chem. 72, 3454 (2007). (http://dx.doi.org/10.1021/jo0626461)
- 4. J. I. Seeman, J. B. Paine III, H. V. Secor, H. S. Im, E. R. Bernstein. J. Am. Chem. Soc. 114, 5269 (1992). (http://dx.doi.org/10.1021/ja00039a044)
- 5. M. G. Organ, J. T. Cooper, L. R. Rogers, F. Soleymanzadeh, T. Paul. J. Org. Chem. 65, 7959 (2000). (http://dx.doi.org/10.1021/jo001045l)
- 6. Y. Mori, M. Asai, J.-i. Kawade, H. Furukawa. Tetrahedron 51, 5315 (1995). (http://dx.doi.org/10.1016/0040-4020(95)00215-T)
- 7. W. R. Roush, J. A. Straub, M. S. VanNieuwenhze. J. Org. Chem. 56, 1638 (1991).
- 8. (a). M. Larcheveque, A. Debal. Synth. Commun. 10, 49 (1980); (http://dx.doi.org/10.1080/00397918008080053)
- 8. (b). S. K. Taylor, D. DeYoung, L. J. Simons, J. R. Vyvyan, M. A. Wemple, N. K. Wood. Synth. Commun. 28, 1691 (1998). (http://dx.doi.org/10.1080/00397919808006873)
- 9. In parallel with our work, Shair reached the same conclusion about the relative configuration of the spiro center of the ritterazines: S. T. Phillips, M. D. Shair. J. Am. Chem. Soc. 129, 6589 (2007). (http://dx.doi.org/10.1021/ja0705487)
- 10. (a). W. A Nugent, D. F Taber. J. Am. Chem. Soc. 111, 6435 (1989); (http://dx.doi.org/10.1021/ja00198a073)
- 10. (b). D. F. Taber, J. P. Louey, Y. Wang, W. A. Nugent, D. A. Dixon, R. L. Harlow. J. Am. Chem. Soc. 116, 9457 (1994). (http://dx.doi.org/10.1021/ja00100a007)
- 11. (a). E. Negishi, S. R. Miller. J. Org. Chem. 54, 6014 (1989); (http://dx.doi.org/10.1021/jo00287a008)
- 11. (b). D. F. Taber, Y. Wang. J. Am. Chem. Soc. 119, 22 (1997); (http://dx.doi.org/10.1021/ja962162u)
- 11. (c). D. F. Taber, W. Zhang, C. L. Campbell, A. R. Rheingold, C. D. Incarvito. J. Am. Chem. Soc. 122, 4813 (2000). (http://dx.doi.org/10.1021/ja992491x)
- 12. D. R. Kanis, M. A. Ratner, T. J. Marks, M. C. Zerner. Chem. Mater. 3, 19 (1991). Both ZINDO and MOPAC were used as implemented on a Tektronix CAChe workstation. (http://dx.doi.org/10.1021/cm00013a009)
- 13. D. F. Taber, J. Liang. J. Org. Chem. 72, 4313 (2007). (http://dx.doi.org/10.1021/jo062672z)
- 14. (a). H. Suzuki, T. Kawaguchi, K. Takaoka. Bull. Chem. Soc. Jap. 59, 665 (1986); (http://dx.doi.org/10.1246/bcsj.59.665)
- 14. (b). J. U. Jeong, S. C. Sutton, S. Kim, P. L. Fuchs. J. Am. Chem. Soc. 117, 10157 (1995). (http://dx.doi.org/10.1021/ja00145a045)
- 15. D. F. Taber, P. W. DeMatteo, K. V. Taluskie. J. Org. Chem. 72, 1492 (2007). (http://dx.doi.org/10.1021/jo061935m)
- 16. D. F. Taber, C. G. Nelson. J. Org. Chem. 71, 8973 (2006). (http://dx.doi.org/10.1021/jo061420v)