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dc.contributor.authorBallini, Roberto-
dc.contributor.authorBosica, Giovanna-
dc.contributor.authorFiorini, Dennis-
dc.contributor.authorRighi, Paolo-
dc.date.accessioned2017-12-20T10:46:36Z-
dc.date.available2017-12-20T10:46:36Z-
dc.date.issued2002-
dc.identifier.citationBallini, R., Bosica, G., Fiorini, D., & Righi, P. (2002). Nitroalkanes and dimethyl maleate as source of 3-alkyl succinic anhydrides and (E)-3-alkylidene succinic anhydrides. Synthesis, 5, 681-685.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/24914-
dc.description.abstractNitroalkanes react with dimethyl maleate giving a tandem Michael addition/elimination of nitrous acid. The obtained (E)-2-alkylidene dimethyl succinates are: (i) reduced to the corresponding 2-alkyl dimethyl succinates which after hydrolysis produce 1,4-dicarboxylic acids that are prone to convert into the corresponding 3-alkyl succinic anhydrides or (ii) hydrolysed to (E)-2-alkylidene-succinic acids that are easily cyclised to (E)-3-alkylidene succinic anhydrides.en_GB
dc.language.isoenen_GB
dc.publisherGeorg Thieme Verlagen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectNitroalkanesen_GB
dc.subjectHeterocyclic compoundsen_GB
dc.subjectChemical reactionsen_GB
dc.titleNitroalkanes and dimethyl maleate as source of 3-alkyl succinic anhydrides and (E)-3-alkylidene succinic anhydridesen_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-2002-23548-
dc.publication.titleSynthesisen_GB
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