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dc.contributor.authorBarker, Sarah F.
dc.contributor.authorAngus, Donald
dc.contributor.authorTaillefumier, Claude
dc.contributor.authorProbert, Michael R.
dc.contributor.authorWatkin, David J.
dc.contributor.authorWatterson, Mark P.
dc.contributor.authorClaridge, Timothy D. W.
dc.contributor.authorHungerford, Natasha Lynn
dc.contributor.authorFleet, George W. J.
dc.date.accessioned2009-07-10
dc.date.accessioned2014-04-14T23:17:38Z
dc.date.accessioned2017-03-02T00:01:03Z
dc.date.available2017-03-02T00:01:03Z
dc.date.issued2001
dc.date.modified2014-04-14T23:17:38Z
dc.identifier.issn0040-4039
dc.identifier.doi10.1016/S0040-4039(01)00660-8
dc.identifier.urihttp://hdl.handle.net/10072/58345
dc.description.abstractEfficient synthesis of both cis- and trans-3-azido-oxetane-2-carboxylates relies upon efficient nucleophilic displacements of 3-O-triflates of oxetanes by trifluoroacetate and azide. Such structures are scaffolds for incorporation of oxetane-β-amino acids into oligomers; the synthesis of a series of protected β-hexapeptides and the X-ray crystal structure of methyl 2,4-anhydro-6-deoxy-5-O-benzyl-l-altronate are reported.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.publisherElsevier Ltd
dc.publisher.placeOxford, UK
dc.relation.ispartofpagefrom4247
dc.relation.ispartofpageto4250
dc.relation.ispartofjournalTetrahedron Letters
dc.relation.ispartofvolume42
dc.subject.fieldofresearchOrganic Chemical Synthesis
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry
dc.subject.fieldofresearchOrganic Chemistry
dc.subject.fieldofresearchcode030503
dc.subject.fieldofresearchcode0304
dc.subject.fieldofresearchcode0305
dc.titleCis- and trans-3-Azido-Oxetan-2-Carboxylate Scaffolds: Hexamers of Oxetane cis-b-Amino Acids.
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codec1x
gro.facultyFaculty of Science, Environment, Engineering and Technology
gro.date.issued2001
gro.hasfulltextNo Full Text
gro.griffith.authorHungerford, Natasha L.


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