An enantioselective synthesis of carbafuranose sugars based on a linchpin carbacyclisation approach
An enantioselective synthesis of carbafuranose sugars based on a linchpin carbacyclisation approach
Enantiopure carbafuranose derivatives were synthesised via a linchpin carbacyclisation process starting from 1,4-bisepoxides. Both 2-deoxy and 2-deoxy-6-hydroxycarbafuranose derivatives were obtained, which were converted to suitably protected precursors for carbanucleoside synthesis.
821-831
Leung, Leo M.H.
c5dca465-0459-416b-8713-ef0ff4f659fd
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Gibson, Vicky
c2078543-eead-4d7e-9e4b-be193c78f09e
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
7 May 2009
Leung, Leo M.H.
c5dca465-0459-416b-8713-ef0ff4f659fd
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Gibson, Vicky
c2078543-eead-4d7e-9e4b-be193c78f09e
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
Leung, Leo M.H., Light, Mark E., Gibson, Vicky and Linclau, Bruno
(2009)
An enantioselective synthesis of carbafuranose sugars based on a linchpin carbacyclisation approach.
[in special issue: Celebration of the 65th Birthday of Professor George Flee]
Tetrahedron: Asymmetry, 20 (6-8), .
(doi:10.1016/j.tetasy.2009.02.019).
Abstract
Enantiopure carbafuranose derivatives were synthesised via a linchpin carbacyclisation process starting from 1,4-bisepoxides. Both 2-deoxy and 2-deoxy-6-hydroxycarbafuranose derivatives were obtained, which were converted to suitably protected precursors for carbanucleoside synthesis.
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Published date: 7 May 2009
Additional Information:
Dedicated to Professor George Fleet on the occasion of his 65th birthday.
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Local EPrints ID: 67648
URI: http://eprints.soton.ac.uk/id/eprint/67648
ISSN: 0957-4166
PURE UUID: d653dff6-ad85-49fb-ba7d-e10dee519f9c
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Date deposited: 02 Sep 2009
Last modified: 14 Mar 2024 02:44
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Contributors
Author:
Leo M.H. Leung
Author:
Vicky Gibson
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