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Thieme eJournals / AbstractContact Us
PAPERSynthesis 2003: 2189-2193
DOI: 10.1055/s-2003-41017

© Georg Thieme Verlag Stuttgart · New York

 

Efficient Addition of Allylsilanes to α,β-Enones Using Catalytic Indium and Trimethylsilyl Chloride
 
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;
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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