Skeletal rearrangement of a bicylic 1,3-diphenyltrisilane during acid-induced dephenylation reactions
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Materials Science,General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s11201-006-9022-7.pdf
Reference12 articles.
1. (a) Tsuji, H., Fukazawa, A., Yamaguchi, S., Toshimitsu, A. & Tamao, K. 2004 Organometallics 23, 3375–3377; (b) Fukazawa, A., Tsuji, H. & Tamao, K. 2006 J. Am. Chem. Soc. 128, 6800–6801.
2. (a) Tamao, K., Tsuji, H., Terada, M., Asahara, M., Yamaguchi, S. & Toshimitsu, A. 2000 Angew. Chem. Int. Ed. 39, 3287–3290; (b) Tsuji, H., Terada, M., Toshimitsu, A. & Tamao, K. 2003 J. Am. Chem. Soc. 125, 7486–7487; (c) Mallesha, H., Tsuji, H. & Tamao, K. 2004 Organometallics 23, 1639–1642.
3. IMesRCl2(PCy3)(CHPh); IMes = 1,3-dimesityl-4,5-dihydroimi- dazol-2-ylidene; (a) Scholl, M., Ding, S., Lee, C.W. & Grubbs, R.H. 1999 Org. Lett. 1, 953–956; (b) Tranka, T.M. & Grubbs, R.H. 2001 Ace. Chem. Res. 34, 18–29.
4. (a) Kaufmann, D. 1987 Chem. Ber. 120, 853–854; (b) Gross, U. & Kaufmann, D. 1987 Chem. Ber. 120, 991–994; (c) Einholz, W., Gollinger, W. & Haubold, W. 1990 Z. Naturforsch. 45b, 25–30.
5. A recent report demonstrated that the reaction of permethylbicyclo[2.2.2]octasilane with BC13 accomplished the selective chlorination at the bridgehead position without skeletal rearrangement. Setaka, W., Hamada, N. & Kira, M. 2004 Chem. Lett. 33, 626–627.
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