1. Intramolecular rearrangements of silenes II . Synthesis of 1-methyl-1-hydro-1-silaacenaphthene from 1-methyl-1-naphthyl-1-silacyclobutane via [4 → 2 + 2]thermocyclodecomposition — transient silene rearrangement sequence. Novel 1,4-hydrogen shift from aryl carbon to sp2 silicon of the silicon-carbon double bond
2. (b) Gusel'nikov, L. E.; Buravtsev, N. N.; Volkova, V. V.; Zubarev, Yu. E.; Buravtseva, E. N.; Pestunovich, V. A.; Lazareva, N. F. 30th Organosilicon Symposium, May 30−31, 1997, London, Western Ontario, Canada; Abstracts, p A-24.
3. Recent reviews on silenes and related compounds: (a) Raabe, G.; Michl, J. InThe Chemistry of Organic Silicon Compounds; Rappoport, Z., Patai, S., Eds.; Wiley: New York, 1989; Vol. 1, p 1015. (b) Gusel'nikov, L. E.; Avakyan, V. G.Sov. Sci. Rev., B: Chem.1989,13, 39. (c) Brook, A. G.; Brook, M. A.Adv. Organomet. Chem.1995,39, 125. (d) Müller, T.; Ziche, W.; Auner, N. InThe Chemistry of Organic Silicon Compounds; Rappoport, Z., Patai, S., Eds.; Wiley: New York, 1998; Vol. 2, p 857.
4. (a) Gusel'nikov, L. E.; Nametkin, N. S. InAdvances in OrganosiliconChemistry; Voronkov, M. G., Ed.; Mir Publishers: Moscow, 1985; p 69.