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

Roe, C., Sandoe, E. J. and Stephenson, G. R. ORCID: https://orcid.org/0000-0003-1487-9178 (2010) Solvolysis reactions at the 13th carbon of 1-aryl organoiron complexes. Tetrahedron Letters, 51 (4). pp. 591-595. ISSN 0040-4039

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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
UEA Research Groups:	Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Materials and Catalysis
Depositing User:	Rachel Smith
Date Deposited:	08 Jun 2011 10:44
Last Modified:	23 Oct 2022 01:37
URI:	https://ueaeprints.uea.ac.uk/id/eprint/32018
DOI:	10.1016/j.tetlet.2009.11.052

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