Enantioselective synthesis of tetrafluorinated ribose and fructose
Enantioselective synthesis of tetrafluorinated ribose and fructose
A perfluoroalkylidene lithium mediated cyclisation approach for the enantioselective synthesis of a tetrafluorinated aldose (ribose) and of a tetrafluorinated ketose (fructose), both in the furanose and in the pyranose form, is described.
803-814
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
Boydell, A. James
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Timofte, Roxana S.
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Brown, Kylie J.
4fa05c54-c25b-46c8-a521-2d5f9514aae7
Vinader, Victoria
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Weymouth-Wilson, Alexander C.
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February 2009
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
Boydell, A. James
e7ecce9e-6700-4ace-91e6-cc648b353caf
Timofte, Roxana S.
3f3248ca-0730-48fe-b2b4-b6fa52b499f2
Brown, Kylie J.
4fa05c54-c25b-46c8-a521-2d5f9514aae7
Vinader, Victoria
22cfbaf8-9605-4326-8bbe-9a7f0c39f067
Weymouth-Wilson, Alexander C.
d1614b73-6066-4dd1-88b6-90f6e3fb48e2
Linclau, Bruno, Boydell, A. James, Timofte, Roxana S., Brown, Kylie J., Vinader, Victoria and Weymouth-Wilson, Alexander C.
(2009)
Enantioselective synthesis of tetrafluorinated ribose and fructose.
Organic & Biomolecular Chemistry, 7 (4), .
(doi:10.1039/b817260a).
Abstract
A perfluoroalkylidene lithium mediated cyclisation approach for the enantioselective synthesis of a tetrafluorinated aldose (ribose) and of a tetrafluorinated ketose (fructose), both in the furanose and in the pyranose form, is described.
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Published date: February 2009
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Local EPrints ID: 147915
URI: http://eprints.soton.ac.uk/id/eprint/147915
ISSN: 1477-0520
PURE UUID: 1f72c717-585d-461b-9d3f-51d5471352e9
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Date deposited: 27 Apr 2010 08:31
Last modified: 14 Mar 2024 02:44
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Contributors
Author:
A. James Boydell
Author:
Roxana S. Timofte
Author:
Kylie J. Brown
Author:
Victoria Vinader
Author:
Alexander C. Weymouth-Wilson
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