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dc.contributor.authorAitken, R Alan
dc.contributor.authorBloomfield, Charles
dc.contributor.authorMcGeachie, Liam J. R.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.date.accessioned2020-02-17T11:30:01Z
dc.date.available2020-02-17T11:30:01Z
dc.date.issued2020-02-17
dc.identifier.citationAitken , R A , Bloomfield , C , McGeachie , L J R & Slawin , A M Z 2020 , ' Diethyl pyrrole-2,5-dicarboxylate ' , Molbank , vol. 2020 , no. 1 , M1117 . https://doi.org/10.3390/M1117en
dc.identifier.issn1422-8599
dc.identifier.otherPURE: 266390594
dc.identifier.otherPURE UUID: f7e3dcc3-51b0-4b2c-887b-5a2a5d3c1383
dc.identifier.otherORCID: /0000-0002-9527-6418/work/69463241
dc.identifier.otherORCID: /0000-0001-6959-5311/work/69463341
dc.identifier.otherScopus: 85081272816
dc.identifier.otherWOS: 000523436200018
dc.identifier.urihttps://hdl.handle.net/10023/19479
dc.description.abstractThe title compound has been obtained in moderate yield by a new and unexpected base-induced ring contraction from a 1,4-thiazine precursor. Its X-ray structure showing hydrogen bonded dimers is compared with those of other crystallographically characterized 2-acylpyrroles.
dc.format.extent6
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.rightsCopyright © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en
dc.subjectDiethyl pyrrole-2,5-dicarboxylateen
dc.subjectX-ray structureen
dc.subjectHydrogen bondingen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleDiethyl pyrrole-2,5-dicarboxylateen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.3390/M1117
dc.description.statusPeer revieweden
dc.identifier.urlhttps://www.mdpi.com/1422-8599/2020/1/M1117en


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