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Crystal Structures of 2-Phenyl-2H-1,2,3-Triazol-4-Carbaldehyde, an Active a-Glycosidase Inhibition Agent, and (1-Phenyl-1H-1,2,3-Triazol-4-yl)Methyl Benzoate and (2-(4-Fluorophenyl)-2H-1,2,3-Triazole-4-yl)Methanol, Two Moderately Active Compounds

dc.contributor.authorGonzaga, Daniel
dc.contributor.authorda Silva, Fernando C.
dc.contributor.authorFerreira, Vitor F.
dc.contributor.authorWardell, James L.
dc.contributor.authorWardell, Solange M. S. V.
dc.date.accessioned2016-02-15T17:00:14Z
dc.date.available2016-02-15T17:00:14Z
dc.date.issued2016-02
dc.identifier60023874
dc.identifierbcc60d43-2858-4cc6-a8d4-7eaa74955568
dc.identifier84956819238
dc.identifier.citationGonzaga , D , da Silva , F C , Ferreira , V F , Wardell , J L & Wardell , S M S V 2016 , ' Crystal Structures of 2-Phenyl-2H-1,2,3-Triazol-4-Carbaldehyde, an Active a-Glycosidase Inhibition Agent, and (1-Phenyl-1H-1,2,3-Triazol-4-yl)Methyl Benzoate and (2-(4-Fluorophenyl)-2H-1,2,3-Triazole-4-yl)Methanol, Two Moderately Active Compounds ' , Journal of Chemical Crystallography , vol. 46 , no. 2 , pp. 67-76 . https://doi.org/10.1007/s10870-015-0629-4en
dc.identifier.issn1074-1542
dc.identifier.urihttp://hdl.handle.net/2164/5517
dc.descriptionThe use of the NCS crystallographic service at Southampton and the valuable assistance of the staff there are gratefully acknowledged. JLW thanks FAPERJ, Brazil for support.en
dc.format.extent10
dc.format.extent1617650
dc.language.isoeng
dc.relation.ispartofJournal of Chemical Crystallographyen
dc.subject1H-1,2,3-triazoleen
dc.subject2H-1,2,3-triazoleen
dc.subjectα-glycosidase inhibitionen
dc.subjectHydrogen bonds, π···π interactionsen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleCrystal Structures of 2-Phenyl-2H-1,2,3-Triazol-4-Carbaldehyde, an Active a-Glycosidase Inhibition Agent, and (1-Phenyl-1H-1,2,3-Triazol-4-yl)Methyl Benzoate and (2-(4-Fluorophenyl)-2H-1,2,3-Triazole-4-yl)Methanol, Two Moderately Active Compoundsen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.University of Aberdeenen
dc.contributor.institutionUniversity of Aberdeen.Chemistryen
dc.description.statusPeer revieweden
dc.identifier.doi10.1007/s10870-015-0629-4


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