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| PAPER | Synthesis 2003: 2189-2193 DOI: 10.1055/s-2003-41017 |
© Georg Thieme Verlag Stuttgart · New York
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Efficient Addition of Allylsilanes to α,β-Enones Using Catalytic Indium and Trimethylsilyl Chloride
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| Phil Ho Lee*, Dong Seomoon, Sundae Kim, K. Nagaiah, S. V. Damle, Kooyeon Lee |
Department of Chemistry, Kangwon National University, Chunchon 200-701, Republic of Korea Fax: +82(33)2537582; e-Mail: phlee@kangwon.ac.kr;
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Received
3 June 2003 |
Abstract
α,β-Enones undergo an efficient Hosomi-Sakurai reaction with allyltrimethylsilane, in which a catalytic amount of indium is used in the presence of trimethylsilyl chloride as an activator under mild conditions to produce the conjugate addition products in good yields. Key words
addition reactions - catalysis - indium - Michael additions - silicon
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