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).

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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
Digital Object Identifier (DOI): doi:10.1039/b701548h
ISSNs: 1359-7345 (print)
Keywords: cyclization, dihydroxylation, ad, alcohols, polyether ionophore antibiotics, strategy, rearrangement, acid, geiparvarin analogs
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ePrint ID: 54341
Date :
Date Event
2007Published
Date Deposited: 31 Jul 2008
Last Modified: 16 Apr 2017 17:47
Further Information:Google Scholar
URI: http://eprints.soton.ac.uk/id/eprint/54341

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