Silyation de derives carbonyles α,β-acetyleniques. Synthese d'allenoxysilanes

作者: G. Merault , P. Bourgeois , J. Dunogues , N. Duffaut

DOI: 10.1016/S0022-328X(00)90310-3

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摘要: Abstract In the presence of magnesium and in hexamethylphosphoric triamide (HMPT), trimethylchlorosilane reacts with α,β-acetylenic ketones to give most cases 1,4 addition two trimethylsilyl groups conjugated system: allenoxysilanes, which constitute a new class organometallic compounds, are formed. These upon hydrolysis corresponding silylated α,β-ethylenic ketones. Other reactions also take place: complete reduction carbonyl group giving polysilylated allenes; reductive duplication accompanied by O-silylation, enolization. α,β-Acetylenic aldehydes same type reactions.

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