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Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24915
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dc.contributor.authorBallini, Roberto-
dc.contributor.authorBosica, Giovanna-
dc.contributor.authorUselli, Alessandra-
dc.date.accessioned2017-12-20T10:47:36Z-
dc.date.available2017-12-20T10:47:36Z-
dc.date.issued1994-
dc.identifier.citationBallini, R., Bosica, G., & Uselli, A. (1994). A simple, efficient, two-step synthesis of symmetric 2,7-dialkyl-1,6-dioxaspiro[4.4]nonanes. Journal of Heterocyclic Chemistry, 31(1), 259-260.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/24915-
dc.description.abstractA two-step synthesis of symmetric 2,7-dialkyl-1,6-dioxaspiro[4.4]nonanes has been achieved by double Michael addition of nitromethane with two moles of enones on Amberlyst A21, followed by in situ reduction with sodium borohydride, then spontaneous spiroketalization of the obtained nitrodiol, by the Nef reaction under acidic conditions, affords the title compounds in good yields.en_GB
dc.language.isoenen_GB
dc.publisherWiley-Blackwell Publishing, Inc.en_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectAsymmetric synthesisen_GB
dc.subjectChemical reactionsen_GB
dc.titleA simple, efficient, two-step synthesis of symmetric 2,7-dialkyl-1,6-dioxaspiro[4.4]nonanesen_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.doi10.1002/jhet.5570310145-
dc.publication.titleJournal of Heterocyclic Chemistryen_GB
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