The University of Southampton
University of Southampton Institutional Repository

An enantioselective synthesis of carbafuranose sugars based on a linchpin carbacyclisation approach

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.
0957-4166
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
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), 821-831. (doi:10.1016/j.tetasy.2009.02.019).

Record type: Article

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.

Full text not available from this repository.

More information

Published date: 7 May 2009
Additional Information: Dedicated to Professor George Fleet on the occasion of his 65th birthday.

Identifiers

Local EPrints ID: 67648
URI: http://eprints.soton.ac.uk/id/eprint/67648
ISSN: 0957-4166
PURE UUID: d653dff6-ad85-49fb-ba7d-e10dee519f9c
ORCID for Mark E. Light: ORCID iD orcid.org/0000-0002-0585-0843
ORCID for Bruno Linclau: ORCID iD orcid.org/0000-0001-8762-0170

Catalogue record

Date deposited: 02 Sep 2009
Last modified: 05 Nov 2019 01:56

Export record

Altmetrics

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×