Oxy-Cope rearrangements of fluorinated divinylcyclohexanols: a modular method for the construction of selectively fluorinated cyclic ketones

Dimartino, Gianluca, Percy, Jonathan M., Spencer, Neil S., Gelbrich, Thomas, Hursthouse, Michael B. and Light, Mark E. (1999) Oxy-Cope rearrangements of fluorinated divinylcyclohexanols: a modular method for the construction of selectively fluorinated cyclic ketones. Chemical Communications, (24), 2535-2536. (doi:10.1039/a908450i).

Record type: Article

Abstract

Oxy-Cope rearrangements of fluorinated divinylcyclohexanols afford access to cyclodecenones containing from two to five fluorine atoms.

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Published date: 1999

Keywords: -sigmatropic rearrangements, enol systems, mechanism

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Identifiers

Local EPrints ID: 39131

URI: http://eprints.soton.ac.uk/id/eprint/39131

DOI: doi:10.1039/a908450i

ISSN: 1359-7345

PURE UUID: bad02d10-4ea3-442c-b603-a2f9521d983d

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Date deposited: 17 Jul 2006

Last modified: 15 Mar 2024 08:11

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Contributors

Author: Gianluca Dimartino

Author: Jonathan M. Percy

Author: Neil S. Spencer

Author: Thomas Gelbrich

Author: Michael B. Hursthouse

Author: Mark E. Light

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