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Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/27597
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dc.contributor.authorBallini, Roberto-
dc.contributor.authorBosica, Giovanna-
dc.contributor.authorPalmieri, Alessandro-
dc.contributor.authorPizzo, Ferdinando-
dc.contributor.authorVaccaro, Luigi-
dc.date.accessioned2018-03-02T14:35:28Z-
dc.date.available2018-03-02T14:35:28Z-
dc.date.issued2008-
dc.identifier.citationBallini, R., Bosica, G., Palmieri, A., Pizzo, F., & Vaccaro, L. (2008). Isolute® si-carbonate catalyzes the nitronate addition to both aldehydes and electron-poor alkenes under solvent-free conditions. Green Chemistry, 10(5), 541-544.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/27597-
dc.description.abstractIt has been found that commercial ISOLUTE® Si-carbonate catalyzes both nitroaldol and Michael reactions, from nitroalkanes and under solvent-free conditions, allowing satisfactory to good yields of nitroalkanols and γ-nitro-functionalized carbonyl and cyano derivatives. In addition, a one-pot Henry-Michael reaction can be performed.en_GB
dc.language.isoenen_GB
dc.publisherThe Royal Society of Chemistryen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectChemical reactionsen_GB
dc.subjectNitroalkanesen_GB
dc.subjectAldehydesen_GB
dc.subjectChemistry, Organicen_GB
dc.subjectCarbonyl compoundsen_GB
dc.titleIsolute®Si-carbonate catalyzes the nitronate addition to both aldehydes and electron-poor alkenes under solvent-free conditionsen_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.doi10.1039/b719477c-
dc.publication.titleGreen Chemistryen_GB
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