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dc.contributor.authorPrichard, Kate L
dc.contributor.authorO'Brien, Nicholas
dc.contributor.authorGhorbani, Mahdi
dc.contributor.authorWood, Adam
dc.contributor.authorBarnes, Evan
dc.contributor.authorKato, Atsushi
dc.contributor.authorHouston, Todd A
dc.contributor.authorSimone, Michela I
dc.date.accessioned2019-06-24T01:57:40Z
dc.date.available2019-06-24T01:57:40Z
dc.date.issued2018
dc.identifier.issn1434-193X
dc.identifier.doi10.1002/ejoc.201801011
dc.identifier.urihttp://hdl.handle.net/10072/385740
dc.description.abstractStereoselective and biocatalysed synthetic routes to 3,4,5‐trihydroxypiperidines and their N‐ and O‐derivatisations are reviewed. These iminosugars effectively modulate glycosidase enzymes and display biological activities in immunosuppression, as anti‐inflammatory agents and as anti‐viral agents. Syntheses to these building blocks and their N‐ and O‐derivatives are predicted to produce drug leads of high Fsp3 index. This is also crucial in the collection of structure‐activity relationship data, particularly for diseases dependant on glycosidase modulation.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofpagefrom6830
dc.relation.ispartofpageto6842
dc.relation.ispartofissue48
dc.relation.ispartofjournalEUROPEAN JOURNAL OF ORGANIC CHEMISTRY
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry
dc.subject.fieldofresearchOrganic Chemistry
dc.subject.fieldofresearchcode0304
dc.subject.fieldofresearchcode0305
dc.titleSynthetic Routes to 3,4,5-Trihydroxypiperidines via Stereoselective and Biocatalysed Protocols, and Strategies to N- and O-Derivatisation
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.hasfulltextNo Full Text
gro.griffith.authorHouston, Todd A.


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