Regioselective synthesis of bis(silyl enol ethers) and bis(conjugated enones) through electron transfer from Mg metal |
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Authors: | Hirofumi Maekawa |
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Affiliation: | Department of Chemistry, Nagaoka University of Technology, 1603-1 Kamitomiokacho, Nagaoka, Niigata 940-2188, Japan |
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Abstract: | Treatment of α,β-unsaturated ketones with Mg metal in the presence of trimethylsilyl choride (TMSCl) brought about facile and regioselective reductive dimerization to give the corresponding bis(silyl enol ethers), 1,6-bis(trimethylsilyloxy)-1,5-dienes. Similar Mg-promoted reductive dimerization of 1,3-cyclic diketones in the presence of TMSCl followed by acid-catalyzed hydrolysis led to selective formation of the corresponding 1,6-diketo-2,4-dienes in moderate to good yields. |
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Keywords: | Dimerization Electron transfer Enol ethers Magnesium and compounds |
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