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dc.contributor.authorBhatt, Beenuen_US
dc.contributor.authorThomson, Robinen_US
dc.contributor.authorvon Itzstein, Marken_US
dc.date.accessioned2017-05-03T15:55:45Z
dc.date.available2017-05-03T15:55:45Z
dc.date.issued2011en_US
dc.date.modified2012-02-14T05:37:06Z
dc.identifier.issn00404039en_US
dc.identifier.doi10.1016/j.tetlet.2011.03.090en_US
dc.identifier.urihttp://hdl.handle.net/10072/42611
dc.description.abstractThis Letter describes an efficient synthesis of a range of 10-homo-N-nucleoside mimetics with a series of 4-substituted 1,2,3-triazoles replacing the natural nucleobase. The synthesis of 6-O-monosulfated 10- homo-N-nucleoside mimetic derivatives is also discussed.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_US
dc.languageEnglishen_US
dc.publisherElsevieren_US
dc.publisher.placeUnited Statesen_US
dc.relation.ispartofstudentpublicationNen_US
dc.relation.ispartofpagefrom2741en_US
dc.relation.ispartofpageto2743en_US
dc.relation.ispartofissue21en_US
dc.relation.ispartofjournalTetrahedron Lettersen_US
dc.relation.ispartofvolume52en_US
dc.rights.retentionYen_US
dc.subject.fieldofresearchOrganic Chemical Synthesisen_US
dc.subject.fieldofresearchcode030503en_US
dc.titleAn efficient approach to 2,5-anhydro-glucitol-based 1'-homo-N-nucleoside mimeticsen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyOffice of the Snr Dep Vice Chancellor, Institute for Glycomicsen_US
gro.date.issued2011
gro.hasfulltextNo Full Text


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