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Diethyl pyrrole-2,5-dicarboxylate
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dc.contributor.author | Aitken, R Alan | |
dc.contributor.author | Bloomfield, Charles | |
dc.contributor.author | McGeachie, Liam J. R. | |
dc.contributor.author | Slawin, Alexandra M. Z. | |
dc.date.accessioned | 2020-02-17T11:30:01Z | |
dc.date.available | 2020-02-17T11:30:01Z | |
dc.date.issued | 2020-02-17 | |
dc.identifier | 266390594 | |
dc.identifier | f7e3dcc3-51b0-4b2c-887b-5a2a5d3c1383 | |
dc.identifier | 85081272816 | |
dc.identifier | 000523436200018 | |
dc.identifier.citation | Aitken , 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/M1117 | en |
dc.identifier.issn | 1422-8599 | |
dc.identifier.other | ORCID: /0000-0002-9527-6418/work/69463241 | |
dc.identifier.other | ORCID: /0000-0001-6959-5311/work/69463341 | |
dc.identifier.uri | https://hdl.handle.net/10023/19479 | |
dc.description.abstract | The 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.extent | 6 | |
dc.format.extent | 1513717 | |
dc.language.iso | eng | |
dc.relation.ispartof | Molbank | en |
dc.subject | Diethyl pyrrole-2,5-dicarboxylate | en |
dc.subject | X-ray structure | en |
dc.subject | Hydrogen bonding | en |
dc.subject | QD Chemistry | en |
dc.subject | DAS | en |
dc.subject.lcc | QD | en |
dc.title | Diethyl pyrrole-2,5-dicarboxylate | en |
dc.type | Journal article | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.identifier.doi | https://doi.org/10.3390/M1117 | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | https://www.mdpi.com/1422-8599/2020/1/M1117 | en |
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