1. Stability of regioisomeric sugar allyltins. Cleavage of the carbon oxygen bond under radical conditions
2. For examples of the application of IMDA in the synthesis of carbobicyclic products, see: (a) Fraser-Reid, B.; Benko, Z.; Guiliano, R.; Sun, K. M.; Taylor, N. J. Chem. Soc., Chem. Commun. 1984, 1029–1030; (b) Carruthers, W. Cycloaddition Reactions in Organic Synthesis (Tetrahedron Organic Chemistry Series Vol. 8) 1990, 91–208; (c) Roush, W. R. Advances in Cycloaddition 1990, 2, 91–146 (Curran, D. P., Ed.) and references cited therein; (d) Herczegh, P.; Zsely, M.; Szilagyi, L.; Bajza, I.; Kovacs, A.; Batta, G.; Bognar, R. Cycloaddition Reactions in Organic Chemistry 1992, 112 (ACS Symposium Series 494, Guiliano, R. M., Edition); (e) Kozikowski, A. P.; Tueckmantel, W. J. Org. Chem. 1991, 56, 2826–2837; (f) Craig, D.; Geach, N. J.; Pearson, Ch. J.; Slawin, A. M. Z.; White, A. J. P.; Williams, D. J. Tetrahedron 1995, 51, 6071–6098; (g) Ishikara, K.; Kurihara, H.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 3049–3050; (h) Ainsworth, P. J.; Craig, D.; White, A. J. P.; Williams, D. J. Tetrahedron 1996, 52, 8937–8946; (i) Deagostino, A.; Maddaluno, J.; Prandi, C.; Venturello, P. J. Org. Chem. 1996, 61, 7597–7599; (j) Gwaltney, S. L., II; Sakata, S. T.; Shea, K. J. J. Org. Chem. 1996, 61, 7438–7451; (k) Diedrich, M. K.; Klaerner, F.-G. J. Am. Chem. Soc. 1998, 120, 6212–6218; (l) Evans, D. A.; Barnes, D. M.; Johnson, J. S.; Lectka, Th.; Matt, P.; Miller, S. J.; Murry, J. A.; Norcross, R. D.; Shaughnessy, E. A.; Campos, K. R. J. Am. Chem. Soc. 1999, 121, 7582–7594; (m) Fukunaga, K.; Kunieda, T. Tetrahedron Lett. 1999, 40, 6041–6044; (n) Jung, M. E.; Huang, A. Org. Lett. 2000, 2, 2659–2662; (o) Enholm, E. J.; Jiang, Sh. J. Org. Chem. 2000, 65, 4756–4758; (p) Hayashi, H. In Cycloaddition Reactions in Organic Synthesis; Kobayashi, S.; Jorgensen K. A., Eds.; Wiley-VCH: New York, 2002; pp. 5–55.
3. Tri-n-butyltin cuprate as a tool for the preparation of stannyl derivatives of carbohydrates
4. Intramolecular Diels-Alder reaction of chiral, highly oxygenated trienoates derived from sugar allyltins
5. A convenient route to enantiomerically pure bicyclo[4.3.0]nonanes from sugar allyltin derivatives