Pure and Applied Chemistry

Pure Appl. Chem., 2010, Vol. 82, No. 9, pp. 1773-1783

http://dx.doi.org/10.1351/PAC-CON-09-08-06

Published online 2010-06-04

Development of an efficient synthetic strategy for bioactive alkaloids possessing a spirocyclic ring system

References

• 1. For reviews, see.
• 1a. M. Ochiai. Rev. Heteroatom. Chem. 2, 92 (1989).
• 1b. R. M. Moriarty. Synthesis 431 (1990). (http://dx.doi.org/10.1055/s-1990-26898)
• 1c. R. M. Moriarty, R. K. Vaid, G. E. Koser. Synlett 365 (1990). (http://dx.doi.org/10.1055/s-1990-21097)
• 1d. Y. Kita, H. Tohma, T. Yakura. Trends Org. Chem. 3, 113 (1992).
• 1e. P. J. Stang, V. V. Zhdankin. Chem. Rev. 96, 1123 (1996). (http://dx.doi.org/10.1021/cr940424+)
• 1f. A. Varvogolis. Hypervalent Iodine in Organic Synthesis, Academic Press, San Diego (1997).
• 1g. T. Kitamura, Y. Fujiwara. Org. Prep. Proced. Int. 29, 409 (1997). (http://dx.doi.org/10.1080/00304949709355217)
• 1h. V. V. Zhdankin. ARKIVOC 1 (2009).
• 2. H. Shirafuji, S. Tsubotani, T. Ishimaru, S. Harada. PTC Inc. Appl., 1991, WO91 13,887 [Chem. Abstr. 116, 39780h (1992)].
• 3a. H. Mizutani, J. Takayama, T. Honda. Tetrahedron Lett. 43, 2411 (2002). (http://dx.doi.org/10.1016/S0040-4039(02)00296-4)
• 3b. H. Mizutani, J. Takayama, T. Honda. Heterocycles 62, 343 (2004).
• 4. H. Mizutani, J. Takayama, T. Honda. Synlett 328 (2005).
• 5. D. Widzowski, H. F. Helander, E. S. C. Wu. Drug Discov. Today 2, 341 (1997). (http://dx.doi.org/10.1016/S1359-6446(97)01076-3)
• 6. B. B. Snider, H. Lin. Org. Lett. 2, 643 (2000). (http://dx.doi.org/10.1021/ol991401q)
• 7. D. J. Wardrop, A. Basek. Org. Lett. 3, 1053 (2001). (http://dx.doi.org/10.1021/ol015626o)
• 8. J. M. A. Auty, I. Churcher, C. J. Hayes. Synlett 1443 (2004).
• 9. M. Ousmer, N. A. Braun, C. Bavoux, M. Perrin, M. A. Ciufolini. J. Am. Chem. Soc. 123, 7534 (2001). (http://dx.doi.org/10.1021/ja016030z)
• 10. S. Nagumo, A. Matoba, Y. Ishii, S. Yamaguchi, N. Akutsu, H. Nishijima, A Nishida, N. Kawahara. Tetrahedron 58, 9871 (2002). (http://dx.doi.org/10.1016/S0040-4020(02)01292-9)
• 11. Y. Moritani, D. H. Appella, V. Jurkauskas, S. L. Buchwald. J. Am. Chem. Soc. 122, 6797 (2000). (http://dx.doi.org/10.1021/ja0009525)
• 12. V. V. Berezhinskaya, E. A. Trutneva. Tr. Vses. Nauchno-Issled. Inst. Lek. Rast. 14, 66 (1971).
• 13a. T. Kametani, H. Yagi. Chem. Commun. 366 (1967).
• 13b. T. Kametani, H. Yagi. J. Chem. Soc., Perkin Trans. 2182 (1967).
• 14a. Z. Horii, Y. Nakashita, C. Iwata. Tetrahedron Lett. 12, 1167 (1971). (http://dx.doi.org/10.1016/S0040-4039(01)96655-9)
• 14b. T. Kametani, T. Sugahara, H. Sugi, S. Shibuya, K. Fukumoto. Chem. Commun. 724 (1971).
• 14c. T. Kametani, T. Sugahara, H. Sugi, S. Shibuya, K. Fukumoto. Tetrahedron 27, 5993 (1971). (http://dx.doi.org/10.1016/S0040-4020(01)91764-8)
• 14d. T. Kametani, K. Fukumoto, S. Shibuya, H. Nemoto, T. Nakano, T. Sugahara, T. Takahashi, Y. Aizawa, M. Toriyama. J. Chem. Soc., Perkin Trans. 1 1435 (1972). (http://dx.doi.org/10.1039/p19720001435)
• 14e. Z. Horii, C. Iwata, Y. Nakashita. Chem. Pharm. Bull. 26, 481 (1978).
• 15. S. Ishiwata, K. Itakura, K. Misawa. Chem. Pharm. Bull. 18, 1219 (1970).
• 16. For reviews, see.
• 16a. M. Shamma. Alkaloids (London) 6, 170 (1975).
• 16b. E. K. Stephenson, M. P. Cava. Heterocycles 39, 891 (1994) and refs. cited therein.
• 17. T. Honda, H. Shigehisa. Org. Lett. 8, 657 (2006). (http://dx.doi.org/10.1021/ol052841m)
• 18. Y.-L. Yang, F.-R. Chang, Y.-C. Wu. Helv. Chim. Acta 87, 1392 (2004). (http://dx.doi.org/10.1002/hlca.200490127)
• 19. H. Shigehisa, T. Honda. Tetrahedron Lett. 47, 7301 (2006). (http://dx.doi.org/10.1016/j.tetlet.2006.08.028)
• 20. Russian Pharmacopeia, 10^th ed., Ministry of Health of the USSR, Moscow, pp. 612–614 (1968).
• 21. I. A. Beutler, E. W. Karbon, A. N. Brubaker, R. Malik, D. R. Curtis, S. J. Enna. Brain Res. 330, 135 (1985). (http://dx.doi.org/10.1016/0006-8993(85)90014-9)
• 22. T. Honda, H. Namiki, K. Kaneda, H. Mizutani. Org. Lett. 6, 87 (2004). (http://dx.doi.org/10.1021/ol0361251)
• 23. H. Tatematsu, M. Mori, T.-H. Yang, J.-J. Chang, T. T.-Y. Lee, K.-H. Lee. J. Pharm. Sci. 80, 325 (1991). (http://dx.doi.org/10.1002/jps.2600800408)
• 24. T. Honda, H. Namiki, M. Watanabe, H. Mizutani. Tetrahedron Lett. 45, 5211 (2004). (http://dx.doi.org/10.1016/j.tetlet.2004.05.031)