References
- H. Yamamoto (Ed.), Lewis Acids in Organic Synthesis, Vols. 1 and 2, Wiley-VCH: Weinheim, 2000.
- For reviews of [3+2] cycloaddition reactions of allylsilanes: (a) Masse, C. E.; Panek, J. S. Chem. Rev. 1995, 95, 1293–1316. (b) Chabaud, L.; James, P.; Landais, Y. Eur. J. Org. Chem. 2004, 3173–3199.
- (a) Danheiser, R. L.; Dixon, B. R.; Gleason, R. W. J. Org. Chem. 1992, 57, 6094–6097. (b) Buckle, M. J. C.; Fleming, I.; Gil, S.; Pang, K. L. C. Org. Biomol. Chem. 2004, 2, 749–769.
- Hirabayashi, K.; Sato, H.; Kuriyama, Y.; Matsuo, J.; Sato, T.; Shimizu, T.; Kamigata, N. Chem. Lett. 2007, 36, 826–827.
- The stereochemical assignment was determined by NMR analysis utilizing NOESY experiments.
- In the protodesilylation, HI or acetic acid was usually used. Colvin, E. W. Silicon Reagents in Organic Synthesis, Academic Press: London, 1988; pp. 14–17.
- (a) Wierschke, S. G.; Chandrasekhar, J.; Jorgensen, W. L. J. Am. Chem. Soc. 1985, 107, 1496–1500. (b) Lambert, J. B.; Zhao, Y. J. Am. Chem. Soc. 1996, 118, 7867–7868.