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Pentadienylsilanes as new reagents of the siteselective dienylmethylation of electrophiles promoted by a Lewis acid
Authors:Akira Hosomi  Masaki Saito  Hideki Sakurai
Affiliation:Department of Chemistry, Faculty of Science, Tohoku University, Sendai 980, Japan
Abstract:(2,4-Pentadienyl)- and (2,4-hexadienyl)trimethylsilanes, prepared from the corresponding pentadienylpotassiums and trimethylchlorosilane, react smoothly with various electrophiles such as acetals, aldehydes and acid halides to give pentadienylation products, with regiospecific transposition of the pentadienyl group.
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