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Diethyl (1-benzyl-4-phenyl-3-trifluoromethyl-1Hpyrrol-2-yl)phosphonate

dc.contributor.authorCal, Dariusz
dc.contributor.authorJezuita, Anna
dc.contributor.authorZagórski, Piotr
dc.contributor.authorEjsmont, Krzysztof
dc.contributor.authorZarychta, Bartosz
dc.date.accessioned2021-09-09T11:09:39Z
dc.date.available2021-09-09T11:09:39Z
dc.date.issued2017
dc.identifier.issn2414-3146
dc.identifier.urihttp://hdl.handle.net/11089/39016
dc.description.abstractIn the title compound, C22H23F3NO3P, the dihedral angles between the pyrrole ring and the benzyl and phenyl rings are 81.38 (7) and 46.21 (8)°, respectively. The ethyl phosphate groups present with P—O—C—C torsion angles of −178.47 (10) and 106.72 (16)°, and an intra­molecular C—H...O hydrogen bond occurs. In the extended structure, mol­ecules are linked by C—H...O and C—H...F hydrogen bonds to generate [001] chains.pl_PL
dc.language.isoenpl_PL
dc.publisherW. T. A. Harrison, University of Aberdeen, Scotlandpl_PL
dc.relation.ispartofseriesIUCrData;
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectcrystal structurepl_PL
dc.subjectfluorinated heterocyclespl_PL
dc.subjectphosphonyl grouppl_PL
dc.titleDiethyl (1-benzyl-4-phenyl-3-trifluoromethyl-1Hpyrrol-2-yl)phosphonatepl_PL
dc.typeArticlepl_PL
dc.page.number8pl_PL
dc.contributor.authorAffiliationDepartment of Organic Chemistry, Faculty of Chemistry, University of Lodz, Tamka 12pl_PL
dc.contributor.authorAffiliationFaculty of Chemistry, University of Opole, Oleska 48, 45-052 Opole, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Organic Chemistry, Faculty of Chemistry, University of Lodz, Tamka 12pl_PL
dc.contributor.authorAffiliationFaculty of Chemistry, University of Opole, Oleska 48, 45-052 Opole, Polandpl_PL
dc.contributor.authorAffiliationFaculty of Chemistry, University of Opole, Oleska 48, 45-052 Opole, Polandpl_PL
dc.referencesCal, D. & Zagórski, P. (2011). Phosphorus Sulfur Silicon, 186, 2295–2302.pl_PL
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dc.referencesDang, Q., Brown, B. S., Liu, Y., Rydzewski, R. M., Robinson, E. D., van Poelje, P. D., Reddy, M. R. & Erion, M. D. (2009). J. Med. Chem. 52, 2880–2898.pl_PL
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dc.referencesOxford Diffraction (2008). CrysAlis CCD. Oxford Diffraction Ltd, Abingdon, England.pl_PL
dc.referencesSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.pl_PL
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dc.referencesZeng, Q., Zhang, L., Yang, J., Xu, B., Xiao, Y. & Zhang, J. (2014). Chem. Commun. 50, 4203–4206.pl_PL
dc.identifier.doihttps://doi.org/10.1107/S2414314617011221
dc.disciplinenauki chemicznepl_PL


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