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Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24681
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dc.contributor.authorBosica, Giovanna-
dc.contributor.authorDebono, Anthony John-
dc.date.accessioned2017-12-14T11:13:15Z-
dc.date.available2017-12-14T11:13:15Z-
dc.date.issued2014-
dc.identifier.citationBosica, G., & Debono, A. J. (2014). Uncatalyzed, green aza-Michael addition of amines to dimethyl maleate. Tetrahedron, 70(37), 6607-6612.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/24681-
dc.description.abstractDimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition in comparison to other commonly used electron-deficient alkenes. It reacts efficiently with a variety of aliphatic amines in complete absence of any catalyst and solvent at room temperature. Under these environmentally-friendly conditions, high yields of selectively mono-adducts were obtained within short reaction times.en_GB
dc.language.isoenen_GB
dc.publisherPergamon Pressen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectCatalyst poisoningen_GB
dc.subjectSolvent wastesen_GB
dc.subjectSolventsen_GB
dc.subjectAza compoundsen_GB
dc.titleUncatalyzed, green aza-Michael addition of amines to dimethyl maleateen_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.2014.06.124-
dc.publication.titleTetrahedronen_GB
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