Solvolysis reactions at the 13th carbon of 1-aryl organoiron complexes

Roe, C., Sandoe, E. J. and Stephenson, G. R. (2010) Solvolysis reactions at the 13th carbon of 1-aryl organoiron complexes. Tetrahedron Letters, 51 (4). pp. 591-595. ISSN 0040-4039

Full text not available from this repository. (Request a copy)

Abstract

Acid-catalysed solvolysis procedures exchange protecting groups on benzyl alcohol derivatives in the synthesis of eta(5) 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(eta(4)-diene)iron(0) moiety to provide a novel and high-yielding cyclisation reaction forming a 5a alpha-cyanomethyl-5a,8a-dihydrofluorene tricarbonyliron complex in 96% yield. (C) 2009 Elsevier Ltd. All rights reserved.

Item Type: Article
Additional Information: Roe, Caroline Sandoe, Elizabeth J. Stephenson, G. Richard
Faculty \ School: Faculty of Science > School of Chemistry
University of East Anglia > Faculty of Science > Research Groups > Synthetic Chemistry
Depositing User: Rachel Smith
Date Deposited: 08 Jun 2011 11:44
Last Modified: 25 Jul 2018 04:31
URI: https://ueaeprints.uea.ac.uk/id/eprint/32018
DOI: 10.1016/j.tetlet.2009.11.052

Actions (login required)

View Item