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Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/113084
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dc.contributor.authorPintea, Monica-
dc.contributor.authorFazekas, Marijana-
dc.contributor.authorLameiras, Pedro-
dc.contributor.authorCadis, Adrian-Ionut-
dc.contributor.authorBerghian, Camelia-
dc.contributor.authorSilaghi-Dumitrescu, Ioan-
dc.contributor.authorPopa, Flavia-
dc.contributor.authorBele, Constantin-
dc.contributor.authorPle, Nelly-
dc.contributor.authorDarabantu, Mircea-
dc.date.accessioned2023-09-14T10:47:48Z-
dc.date.available2023-09-14T10:47:48Z-
dc.date.issued2008-
dc.identifier.citationPintea, M., Fazekas, M., Lameiras, P., Cadis, I., Berghian, C., Silaghi-Dumitrescu, I., ... & Darabantu, M. (2008). Serinolic amino-s-triazines: iterative synthesis and rotational stereochemistry phenomena as N-substituted derivatives of 2-aminopropane-1, 3-diols. Tetrahedron, 64(37), 8851-8870.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/113084-
dc.description.abstractThe iterative synthesis of 2,4,6-triamino-s-triazines (melamines), precursors and dendritic structures, by amination of cyanuric chloride with C-1 versus C-2-substituted 2-aminopropane-1,3-diols (serinols), is comparatively examined. The stereochemistry of the resulting serinolic amino-s-triazines, issued from the restricted rotation about the newly created C(s-triazine)–No bonds, is for the first time discussed in terms of (pro)diastereomerism based on DNMR and DFT calculation data.en_GB
dc.language.isoenen_GB
dc.publisherElsevier Ltden_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectAmino alcoholsen_GB
dc.subjectDendrimersen_GB
dc.subjectMolecules -- Modelsen_GB
dc.subjectNuclear magnetic resonance spectroscopyen_GB
dc.titleSerinolic amino-s-triazines: iterative synthesis and rotational stereochemistry phenomena as N-substituted derivatives of 2-aminopropane-1,3-diolsen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1016/j.tet.2008.06.071-
dc.publication.titleTetrahedronen_GB
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