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Synthesis of all diastereomeric methyl 2,5-anhydro-3-deoxy-hexonates: precursors to C-2-deoxynucleosides and THF-templated gamma- and delta-amino acids

Watterson, Mark P., Edwards, Alison A., Leach, John A., Smith, Martin D., Ichihara, Osamu, Fleet, George W.J. (2003) Synthesis of all diastereomeric methyl 2,5-anhydro-3-deoxy-hexonates: precursors to C-2-deoxynucleosides and THF-templated gamma- and delta-amino acids. Tetrahedron Letters, 44 (31). pp. 5853-5857. E-ISSN 0040-4039. (doi::10.1016/S0040-4039(03)01416-3) (Access to this publication is currently restricted. You may be able to access a copy if URLs are provided) (KAR id:4883)

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Abstract

Efficient syntheses of all diastereomers of methyl 2,5-anhydro-3-deoxy-hexonate from mannono- or gulono-lactones provide precursors for C -nucleosides of 2-deoxyribose and for THF-templated gamma

Item Type: Article
DOI/Identification number: :10.1016/S0040-4039(03)01416-3
Subjects: Q Science
Q Science > QD Chemistry
Divisions: Divisions > Division of Natural Sciences > Medway School of Pharmacy
Depositing User: Alison Edwards
Date Deposited: 23 May 2009 13:54 UTC
Last Modified: 16 Nov 2021 09:43 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/4883 (The current URI for this page, for reference purposes)
Edwards, Alison A.: https://orcid.org/0000-0002-4637-9373
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