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Synthesis of functionalized 1,5-cyclooctadienes by LICKOR metalation

Revell, J. D. and Ganesan, A. (2002) Synthesis of functionalized 1,5-cyclooctadienes by LICKOR metalation Journal of Organic Chemistry, 67, (17), pp. 6250-6252. (doi:10.1021/jo025715u).

Record type: Article

Abstract

1,5-Cyclooctadiene was lithiated under LICKOR superbase conditions followed by reaction with alkyl halides or ethylene oxide to yield 3-substituted 1,5-cyclooetadienes in high yield and purity. This procedure is suitable for preparation of 1,5-cyclooctadienes carrying pendant functional groups for immobilization on solid-phase resins.

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Published date: 23 August 2002
Keywords: 9-borabicyclononane 9-bbn, organic-synthesis, superbases, route

Identifiers

Local EPrints ID: 19843
URI: http://eprints.soton.ac.uk/id/eprint/19843
ISSN: 0022-3263
PURE UUID: 9976a510-efef-495f-9196-2b5350969dc1

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Date deposited: 20 Feb 2006
Last modified: 17 Jul 2017 16:30

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Contributors

Author: J. D. Revell
Author: A. Ganesan

University divisions

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