Simple and stereoselective syntheses of nucleoside analogues with a benzo[c]furan glycone moiety

Article abstract of DOI:10.1080/15257779908041494

A series of d4T analogues have been synthesised in which the 2',3'- didehydro-2',3'-dideoxyribose moiety is replaced by a benzo[c]furan core. A simple strategy has been developed to access a range of compounds for biological screening. In addition, a ster

Full text of DOI:10.1080/15257779908041494

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Nucleosides and Nucleotides
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Simple and Stereoselective Syntheses
of Nucleoside Analogues with a
Benzo[c]furan Glycone Moiety
David F. Ewing a , Noureddine Fahmi a , Grahame Mackenzie a &
Alessandra Pranzo a
a Department of Chemistry , University of Hull , HU6 7RX, UK
Published online: 04 Oct 2006.
To cite this article: David F. Ewing , Noureddine Fahmi , Grahame Mackenzie & Alessandra Pranzo
(1999) Simple and Stereoselective Syntheses of Nucleoside Analogues with a Benzo[c]furan Glycone
Moiety, Nucleosides and Nucleotides, 18:4-5, 559-563, DOI: 10.1080/15257779908041494
To link to this article: http://dx.doi.org/10.1080/15257779908041494
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