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A catalytic asymmetric protocol for the enantioselective synthesis of 3(2H)-furanones

Marson, C.M., Edaan, E., Morrell, J.M., Coles, S.J., Hursthouse, M.B. and Davies, D.T. (2007) A catalytic asymmetric protocol for the enantioselective synthesis of 3(2H)-furanones Chemical Communications, (24), pp. 2494-2496. (doi:10.1039/b701548h).

Record type: Article

Abstract

3(2H)-Furanones can be prepared by a catalytic asymmetric protocol from enynones, which, if electron-rich, require only one reagent and involve two reactions in a single operation—a domino process.

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Published date: 2007
Keywords: cyclization, dihydroxylation, ad, alcohols, polyether ionophore antibiotics, strategy, rearrangement, acid, geiparvarin analogs

Identifiers

Local EPrints ID: 54341
URI: http://eprints.soton.ac.uk/id/eprint/54341
ISSN: 1359-7345
PURE UUID: 093700b0-aec1-47e2-8e83-71a6f87238ef
ORCID for S.J. Coles: ORCID iD orcid.org/0000-0001-8414-9272

Catalogue record

Date deposited: 31 Jul 2008
Last modified: 17 Jul 2017 14:35

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Contributors

Author: C.M. Marson
Author: E. Edaan
Author: J.M. Morrell
Author: S.J. Coles ORCID iD
Author: M.B. Hursthouse
Author: D.T. Davies

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