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Solvolysis reactions at the 13th carbon of 1-aryl organoiron complexes
Authors:Caroline Roe
Affiliation:School of Chemistry, University of East Anglia, Norwich, NR4 7TJ, UK
Abstract:Acid-catalysed solvolysis procedures exchange protecting groups on benzyl alcohol derivatives in the synthesis of η5 1-arylcyclohexadienyliron building blocks for alkaloid synthesis. The reaction proceeds via a carbocation intermediate which can also be intercepted by intramolecular electrophilic addition to the tricarbonyl(η4-diene)iron(0) moiety to provide a novel and high-yielding cyclisation reaction forming a 5aα-cyanomethyl-5a,8a-dihydrofluorene tricarbonyliron complex in 96% yield.
Keywords:Organoiron   Solvolysis   Deprotection   Dihydrofluorene   Electrophilic cyclisation
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