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dc.contributor.authorAitken, R Alan
dc.contributor.authorAitken, Kati Marianne
dc.contributor.authorCarruthers, Phillip G
dc.contributor.authorJean, Marc-Alexandre
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.date.accessioned2013-10-29T13:01:02Z
dc.date.available2013-10-29T13:01:02Z
dc.date.issued2013
dc.identifier.citationAitken , R A , Aitken , K M , Carruthers , P G , Jean , M-A & Slawin , A M Z 2013 , ' 1,4-Oxazine ' Chemical Communications , vol. 49 , no. 97 , pp. 11367-11369 . DOI: 10.1039/c3cc47801gen
dc.identifier.issn1359-7345
dc.identifier.otherPURE: 76927774
dc.identifier.otherPURE UUID: c1578463-dbc2-49a2-a817-dcb52056126b
dc.identifier.otherScopus: 84887506041
dc.identifier.urihttp://hdl.handle.net/10023/4123
dc.description.abstractThe fundamental heterocyclic compound 1,4-oxazine has been generated using FVP. It is the first parent heterocycle among all the possible isomeric oxazines, thiazines and their heavier atom analogues to be characterised spectroscopically, and is shown to exist in solution entirely as the 4H-isomer. X-ray structure determination of the N-Boc precursor shows significant deviations from theoretically predicted geometric parameters.en
dc.format.extent3en
dc.language.isoeng
dc.relation.ispartofChemical Communicationsen
dc.rightsCopyright 2013, the Authors. This open access article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.en
dc.subjectHeterocyclic compounden
dc.subjectFVPen
dc.subject4H-isomeren
dc.subjectN-Boc precursoren
dc.subjectIsomeric oxazinesen
dc.subjectThiazineen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.title1,4-Oxazineen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/c3cc47801g
dc.description.statusPeer revieweden


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