Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24407
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dc.contributor.authorBallini, Roberto-
dc.contributor.authorBosica, Giovanna-
dc.date.accessioned2017-12-06T15:43:16Z-
dc.date.available2017-12-06T15:43:16Z-
dc.date.issued1996-
dc.identifier.citationBallini, R., & Bosica, G. (1996). The Michael reaction of nitroalkanes with conjugated enones in aqueous media. Tetrahedron Letters, 37(44), 8027-8030.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/24407-
dc.description.abstractThe Michael reaction of various nitroalkanes with conjugated enones can be performed in NaOH 0.025 M and in the presence of cetyltrimethylammonium chloride (CTACl) as cationic surfactant, without any organic solvent. Good yields of the products are obtained even with hindered starting materials.en_GB
dc.language.isoenen_GB
dc.publisherPergamon Pressen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectNitroalkanesen_GB
dc.subjectCarbonyl compoundsen_GB
dc.subjectChemical reactionsen_GB
dc.subjectCatalysts -- Analysisen_GB
dc.titleThe Michael reaction of nitroalkanes with conjugated enones in aqueous mediaen_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.doi10.1016/0040-4039(96)01816-3-
dc.publication.titleTetrahedron Lettersen_GB
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