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1,4-bis[2,2-bis(trimethylsilyl)ethenyl] benzene: Regioselective ring opening of its α,β-epoxybis(silane) with some nucleophiles

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JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 694, 期 12, 页码 1907-1911

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2009.01.030

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Vinylbis(silane); Tris(trimethylsilyl) methyllithium; Peterson reaction; alpha,beta-Epoxybis(silane); Ring opening reaction

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The Peterson olefination reaction of terephthalaldehyde with tris(trimethylsilyl) methyllithium, (Me3Si)(3)-CLi, in Et2O gives disubstituted vinylbis(silane) 1 which reacts with MCPBA in CH2Cl2 at r.t. to afford mixture of mono and disubstituted epoxybis(silanes) 3 and 2. Vinylbis(silane) 1 can be completely converted into epoxybis(silane) 2 with an excess amount of MCPBA. The compound 2 was reacted with various reagents such as HX (X = Cl, Br), H2SO4, LiAlH4 and MeLi/CuI and give the related products. (C) 2009 Elsevier B.V. All rights reserved.

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