1. With FeCl3, Ce(NH4)2(NO3)6, CuCl2 or Pb(OAc)4, see: (a) Emerson, G. F.; Mahler, J. E.; Kochhar, R.; Pettit, R. J. Org. Chem. 1964, 29, 3620; (b) Holmes, J. D.; Pettit, R. J. Am. Chem. Soc. 1963, 85, 2531; (c) Thompson, D. J. J. Organomet. Chem. 1976, 108, 381; (d) Brener, L.; McKennis, J. S.; Pettit, R. Org. Synth. 1976, 55, 43. With amine N-oxides or H2O2/NaOH, see: (e) Shvo, Y.; Hazum, E. J. Chem. Soc., Chem. Commun. 1974, 336; (f) Franck-Neumann, M.; Heitz, M. P.; Martina, D. Tetrahedron Lett. 1983, 24, 1615; cf. also: (g) Davies, S. G. J. Organomet. Chem. 1979, 179, C5.
2. Cycloöctatetraene Iron Tricarbonyl and Related Compounds1,2
3. Knölker, H. J.; Goesmann, H.; Klauss, R. Angew. Chem. 1999, 111, 727; Angew. Chem., Int. Ed. 1999, 38, 702.
4. Franck-Neumann, M.; Martina, D.; Brion, F. Angew. Chem. 1978, 90, 736; Angew. Chem., Int. Ed. Engl. 1978, 17, 690.
5. Un equivalent synthetique chiral du prenal, le formyl-trimethylenemethane (fer) tricarbonyle. synthese du (r)-(-)-ipsdienol