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1,5,6-Triphenyl-8-oxa-7-selena-6-phosphabicyclo[3.2.1]octane-6-selone

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dc.contributor.authorHua, Guoxiong
dc.contributor.authorLi, Yang
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorWoollins, J Derek
dc.date.accessioned2011-03-05T11:21:25Z
dc.date.available2011-03-05T11:21:25Z
dc.date.issued2008-01
dc.identifier.citationHua , G , Li , Y , Slawin , A M Z & Woollins , J D 2008 , ' 1,5,6-Triphenyl-8-oxa-7-selena-6-phosphabicyclo[3.2.1]octane-6-selone ' , Acta Crystallographica. Section E, Structure reports online , vol. 64 , no. 1 , o184 . https://doi.org/10.1107/S1600536807063945en
dc.identifier.issn1600-5368
dc.identifier.otherPURE: 624810
dc.identifier.otherPURE UUID: 1da43b8c-061a-4edb-92fd-d2266ac0f519
dc.identifier.otherWOS: 000252049300379
dc.identifier.otherScopus: 37849053971
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861565
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779277
dc.identifier.urihttps://hdl.handle.net/10023/1682
dc.description.abstractThe structure of the title compound, C23H21OPSe2, consists of fused puckered five- and six-membered rings, PSeC2O and C5O, respectively, with a C2O bridgehead. The C5O ring adopts a chair conformation, whilst the C2PSeO ring has an envelope conformation.
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofActa Crystallographica. Section E, Structure reports onlineen
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.subjectRay crystal-structuresen
dc.subjectP-SE Heterocyclesen
dc.subjectWoollins reagenten
dc.subject(PHP(SE)(MU-SE))(2)en
dc.subjectCynamidesen
dc.subjectReactivityen
dc.subjectAnionsen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.title1,5,6-Triphenyl-8-oxa-7-selena-6-phosphabicyclo[3.2.1]octane-6-seloneen
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/10.1107/S1600536807063945
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=37849053971&partnerID=8YFLogxKen


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