Issue 24, 1999
From the journal:

Chemical Communications

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

Gianluca Dimartino,   Jonathan M. Percy,   Neil S. Spencer,   Thomas Gelbrich,   Michael B. Hursthouse  and  Mark E. Light  

Abstract

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

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Article information

DOI
https://doi.org/10.1039/A908450I
Article type
Paper

Chem. Commun., 1999, 2535-2536

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

G. Dimartino, J. M. Percy, N. S. Spencer, T. Gelbrich, M. B. Hursthouse and M. E. Light, Chem. Commun., 1999, 2535 DOI: 10.1039/A908450I

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