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), 2494-2496. (doi:10.1039/b701548h).

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Original Publication URL: http://dx.doi.org/10.1039/b701548h

Description/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.

Item Type: Article
ISSNs: 1359-7345 (print)
Related URLs:
Keywords: cyclization, dihydroxylation, ad, alcohols,polyether ionophore antibiotics, strategy, rearrangement, acid, geiparvarin analogs
Subjects: Q Science
Q Science > QD Chemistry
Divisions: University Structure - Pre August 2011 > School of Chemistry
ePrint ID: 54341
Date Deposited: 31 Jul 2008
Last Modified: 27 Mar 2014 18:37
URI: http://eprints.soton.ac.uk/id/eprint/54341

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