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À propos de : Synthesis of Various Silacycles via the Lewis Acid-CatalyzedIntramolecular Trans-Hydrosilylation of Unactivated Alkynes        

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  • Synthesis of Various Silacycles via the Lewis Acid-CatalyzedIntramolecular Trans-Hydrosilylation of Unactivated Alkynes
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  • Various silacycles with vinylsilane framework are synthesized via the Lewis acid-catalyzedintramolecular hydrosilylation of alkynes. The cyclization proceeds in an endo-trans or/and in anexo-trans manner, depending on the substrate structure. This methodology is applicable to thesynthesis of five-, six-, seven-, and eight-membered medium-sized silacycles. Furthermore, it ispossible to obtain a silole derivative via the intramolecular hydrosilylation of the ortho-alkynyl-substituted phenylsilane 10.
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