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dc.contributor.authorLevonis, Stephanen_US
dc.contributor.authorKiefel, Miltonen_US
dc.contributor.authorHouston, Todden_US
dc.contributor.authorHealy, Peteren_US
dc.date.accessioned2017-05-03T11:09:44Z
dc.date.available2017-05-03T11:09:44Z
dc.date.issued2010en_US
dc.date.modified2010-07-20T04:53:59Z
dc.identifier.issn16005368en_US
dc.identifier.doi10.1107/S160053680905421Xen_AU
dc.identifier.urihttp://hdl.handle.net/10072/32416
dc.description.abstractThe title compound, C10H8O3, has been synthesized as part of our investigations into the generation of new antibacterial agents and serves as a building block for the synthesis of compound libraries. The compound crystallizes with two independent molecules in the asymmetric unit. The transoid propynyl ester groups are coplanar with the 2-hydroxybenzoate group with maximum deviations of -0.3507 (3) and 0.1591 (3) Šfor the terminal carbons, with intramolecular O-HO hydrogen bonding providing rigidity to the structure and ensuring that the reactivity of the alkyne is not compromised by steric factors. The propynyl group forms intermolecular C-HO interactions with the phenolic O atom. Supramolecular chains along the b axis are found for both molecules with links by weak O-HO intermolecular interactions in the first independent molecule and C-HO interactions in the second.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.format.extent722290 bytes
dc.format.mimetypeapplication/pdf
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherWiley-Blackwell Publishing, Incen_US
dc.publisher.placeUnited Statesen_US
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefromo226en_US
dc.relation.ispartofpagetoo227en_US
dc.relation.ispartofjournalActa crystallographica. Section E, Structure reports onlineen_US
dc.relation.ispartofvolume66en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchStructural Chemistry and Spectroscopyen_US
dc.subject.fieldofresearchcode030606en_US
dc.title2-Propynyl 2-hydroxybenzoateen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
dcterms.licensehttp://creativecommons.org/licenses/by/2.0/uk/legalcodeen_US
gro.facultyOffice of the Snr Dep Vice Chancellor, Institute for Glycomicsen_US
gro.rights.copyrightCopyright remains with the authors 2010. For information about this journal please refer to the journal's website. All articles published in Acta Crystallographica Section E are open access and distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. See http://creativecommons.org/licenses/by/2.0/uk/legalcodeen_AU
gro.date.issued2010
gro.hasfulltextFull Text


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