Title of article
Solvolysis reactions at the 13th carbon of 1-aryl organoiron complexes
Author/Authors
Roe، نويسنده , , Caroline and Sandoe، نويسنده , , Elizabeth J. and Richard Stephenson، نويسنده , , G.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
5
From page
591
To page
595
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
Deprotection , Solvolysis , Dihydrofluorene , Organoiron , Electrophilic cyclisation
Journal title
Tetrahedron Letters
Serial Year
2010
Journal title
Tetrahedron Letters
Record number
1870826
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