A catalytic asymmetric protocol for the enantioselective synthesis of 3(2H)-furanones
A catalytic asymmetric protocol for the enantioselective synthesis of 3(2H)-furanones
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.
cyclization, dihydroxylation, ad, alcohols, polyether ionophore antibiotics, strategy, rearrangement, acid, geiparvarin analogs
2494-2496
Marson, C.M.
e85f225a-76fa-40bd-bd61-2d6c414f6768
Edaan, E.
a879d6e0-c5b5-4df2-8c03-33f4b5bc7586
Morrell, J.M.
633bb0cf-4f5f-40e9-aa51-4de9be4c5678
Coles, S.J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Hursthouse, M.B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Davies, D.T.
1f239090-3a33-4933-9e08-c78e1b6204ab
2007
Marson, C.M.
e85f225a-76fa-40bd-bd61-2d6c414f6768
Edaan, E.
a879d6e0-c5b5-4df2-8c03-33f4b5bc7586
Morrell, J.M.
633bb0cf-4f5f-40e9-aa51-4de9be4c5678
Coles, S.J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Hursthouse, M.B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Davies, D.T.
1f239090-3a33-4933-9e08-c78e1b6204ab
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), .
(doi:10.1039/b701548h).
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
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Date deposited: 31 Jul 2008
Last modified: 16 Mar 2024 03:05
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Contributors
Author:
C.M. Marson
Author:
E. Edaan
Author:
J.M. Morrell
Author:
D.T. Davies
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