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N-Benzyl-N-(2-hydroxyethyl)-2-(oxazolidin-2-on-3-yl)-2-phenylacetamide
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dc.contributor.author | Aitken, R Alan | |
dc.contributor.author | Logan, Joe S | |
dc.contributor.author | Slawin, Alexandra Martha Zoya | |
dc.date.accessioned | 2022-10-03T16:30:21Z | |
dc.date.available | 2022-10-03T16:30:21Z | |
dc.date.issued | 2022-10-03 | |
dc.identifier.citation | Aitken , R A , Logan , J S & Slawin , A M Z 2022 , ' N -Benzyl- N -(2-hydroxyethyl)-2-(oxazolidin-2-on-3-yl)-2-phenylacetamide ' , Molbank , vol. 2022 , no. 4 , M1458 . https://doi.org/10.3390/M1458 | en |
dc.identifier.issn | 1422-8599 | |
dc.identifier.other | PURE: 281535545 | |
dc.identifier.other | PURE UUID: 06c402b7-7079-48d6-a822-00b792521dd5 | |
dc.identifier.other | ORCID: /0000-0001-6959-5311/work/120433233 | |
dc.identifier.other | ORCID: /0000-0002-9527-6418/work/120433250 | |
dc.identifier.other | Scopus: 85144640791 | |
dc.identifier.other | WOS: 000903462900001 | |
dc.identifier.uri | https://hdl.handle.net/10023/26126 | |
dc.description.abstract | The title compound, obtained by base-induced dimerization of 3-benzyloxazolidin-2-one has been prepared and fully characterised. Its X-ray structure features hydrogen bonded dimers involving the hydroxyl OH and amide carbonyl forming a 14-membered ring. | |
dc.format.extent | 4 | |
dc.language.iso | eng | |
dc.relation.ispartof | Molbank | en |
dc.rights | Copyright: © 2022 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 (https:// creativecommons.org/licenses/by/4.0/). | en |
dc.subject | X-ray structure | en |
dc.subject | Hydrogen bonding | en |
dc.subject | Amide rotamers | en |
dc.subject | QD Chemistry | en |
dc.subject | DAS | en |
dc.subject | MCC | en |
dc.subject.lcc | QD | en |
dc.title | N-Benzyl-N-(2-hydroxyethyl)-2-(oxazolidin-2-on-3-yl)-2-phenylacetamide | en |
dc.type | Journal article | en |
dc.description.version | Publisher PDF | 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/M1458 | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | https://www.mdpi.com/1422-8599/2022/4/M1458 | en |
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