Balasubramanian, R. ; George, M. V. (1975) Alkali metal, alkaline and acidic decomposition of silacyclopentadienes Journal of Organometallic Chemistry, 85 (3). pp. 311-316. ISSN 0022-328X
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00223...
Related URL: http://dx.doi.org/10.1016/S0022-328X(00)80304-6
Abstract
1,1-Dimethyl-2,5-diphenyl-1-silacyclopentadiene and 1,1-dimethyl-2,3,4,5-tetraphenyl-1-silacyclopentadiene (X) are cleaved by sodium hydroxide as well as by hydrochloric acid to give trans, trans-1,4-diphenylbutadiene and cis, cis-1,2,3,4-tetraphenylbutadiene, respectively. Compound X, hexaphenylsilacyclopentadiene and 1-methyl-1,2,3,4,5-pentaphenyl-1-silacyclopentadiene, on treatment with potassium in 1,2-dimethoxyethane gave intensely red colored dianions which on quenching in moist tetrahydrofuran gave rise to α,α'-dibenzylstilbene. A pathway for the reaction is suggested.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
ID Code: | 12692 |
Deposited On: | 11 Nov 2010 09:11 |
Last Modified: | 01 Jun 2011 11:22 |
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