Osborn, H. M. I. ORCID: https://orcid.org/0000-0002-0683-0457 and Turkson, A.
(2009)
Synthesis and NMR spectroscopic analysis of 3-nitro-pyranoside, 3-nitro-septanoside and 4-nitro-septanoside derivatives by condensation of the anion of nitromethane with glycoside.
Tetrahedron Asymmetry, 20 (18).
pp. 2162-2166.
ISSN 0957-4166
doi: 10.1016/j.tetasy.2009.08.004
Abstract/Summary
The utility of the nitroaldol reaction for accessing 3-nitro-pyranoside, 3-nitro-septanoside or 4-nitro-septanoside derivatives, by reaction of the anion of nitromethane with glycoside dialdehydes is demonstrated. Initially, the feasibility of using unprotected glucoside dialdehydes was probed for the synthesis of the septanoside products, but this affoided pyranoside rather than septanoside targets. Subsequent studies utilised protected glycoside dialdehydes within the methodology, which allowed entry into a range of 3-nitro or 4-nitro-septanosides in good yield NMR spectroscopic analysis allowed determination of the stereochemistry of each of the products thus afforded.
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Item Type | Article |
URI | https://reading-clone.eprints-hosting.org/id/eprint/1964 |
Item Type | Article |
Refereed | Yes |
Divisions | Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy > Medicinal Chemistry Research Group |
Uncontrolled Keywords | 7-membered ring sugars; d-glucose; nitro; 3-deoxy-3-nitroheptoseptanosides; substituents; antibiotics; nucleosides; iminosugars; inhibitors; oxidation |
Publisher | Elsevier |
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