Extended scope of in situ iodotrimethylsilane mediated selective reduction of benzylic alcohols
Chemical Communications2001Iss. 13, pp. 1168–1169
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Abstract
Iodotrimethylsilane, generated in situ from chlorotrimethylsilane and sodium iodide in acetonitrile, selectively reduces moderately electron deficient benzylic alcohols to the analogous toluenes; other reduction sensitive functional groups such as ketone, aldehyde, nitrile, and nitro are unaffected.
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