Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24645
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dc.contributor.authorBallini, Roberto-
dc.contributor.authorBosica, Giovanna-
dc.date.accessioned2017-12-12T14:21:37Z-
dc.date.available2017-12-12T14:21:37Z-
dc.date.issued1996-
dc.identifier.citationBallini, R., & Bosica, G. (1996). A new two steps synthesis of α-substituted γ-methyl γ-lactones from nitroalkanes. Synlett, 11, 1115-1116.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/24645-
dc.description.abstractα-Substituted γ-methyl γ-lactones are efficiently prepared, in two steps, by regiospecific Michael addition of nitroalkanes to methyl trans-4-oxo-2-pentenoate in MeCN/DBU followed by chemoselective reduction of the obtained enones with NiCl2⋅6H2O/NaBH4. By this method a variety of functionalized 3,5-disubstituted butyrolactones can be obtained.en_GB
dc.language.isoenen_GB
dc.publisherGeorg Thieme Verlagen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectNitroalkanes -- Synthesisen_GB
dc.subjectChemistry, Analyticen_GB
dc.titleA new two steps synthesis of α-substituted γ-methyl γ-lactones from nitroalkanesen_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.doi10.1055/s-1996-5667-
dc.publication.titleSynletten_GB
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