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Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24897
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dc.contributor.authorBallini, Roberto-
dc.contributor.authorBarboni, Luciano-
dc.contributor.authorBosica, Giovanna-
dc.contributor.authorFiorini, Dennis-
dc.contributor.authorMignini, Emanuela-
dc.contributor.authorPalmieri, Alessandro-
dc.date.accessioned2017-12-20T09:48:18Z-
dc.date.available2017-12-20T09:48:18Z-
dc.date.issued2004-
dc.identifier.citationBallini, R., Barboni, L., Bosica, G., Fiorini, D., Mignini, E., & Palmieri, A. (2004). Fast diastereoselective Baylis–Hillman reaction by nitroalkenes : synthesis of di- and triene derivatives. Tetrahedron, 60(23), 4995-4999.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/24897-
dc.description.abstractThe Baylis–Hillman reaction is performed using nitroalkenes as activated alkenes, ethyl-2-bromomethylacrylate as electrophilic acceptor and DBU as catalyst base. Nitro dienes are obtained in good yields and very short reaction times. Moreover, starting from appropriate nitroalkenes it is possible to realize one pot the synthesis of trienic systems.en_GB
dc.language.isoenen_GB
dc.publisherPergamon Pressen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectNitroalkanesen_GB
dc.subjectNitro compoundsen_GB
dc.subjectAllyl compoundsen_GB
dc.titleFast diastereoselective Baylis–Hillman reaction by nitroalkenes : synthesis of di- and triene derivativesen_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.2004.04.030-
dc.publication.titleTetrahedronen_GB
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