Diastereoselective synthesis of trifluoromethylated 1,3-dioxanes by intramolecular oxa-Michael reaction

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dc.contributor.authorLiliana Becerra‐Figueroa
dc.contributor.authorElodie Brun
dc.contributor.authorMichael Mathieson
dc.contributor.authorLouis J. Farrugia
dc.contributor.authorClaire Wilson
dc.contributor.authorJoëlle Prunet
dc.contributor.authorDiego Gamba‐Sánchez
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T14:19:18Z
dc.date.available2026-03-22T14:19:18Z
dc.date.issued2016
dc.descriptionCitaciones: 14
dc.description.abstractA rapid and simple method to access trifluoromethylated 1,3-dioxanes by a sequence of addition/oxa-Michael reaction has been developed; the reaction proceeds smoothly with excellent stereoselectivity.
dc.identifier.doi10.1039/c6ob02333a
dc.identifier.urihttps://doi.org/10.1039/c6ob02333a
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/45831
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofOrganic & Biomolecular Chemistry
dc.sourceSecretaría de Salud de Bogotá
dc.subjectChemistry
dc.subjectMichael reaction
dc.subjectIntramolecular force
dc.subjectStereochemistry
dc.subjectCombinatorial chemistry
dc.titleDiastereoselective synthesis of trifluoromethylated 1,3-dioxanes by intramolecular oxa-Michael reaction
dc.typearticle

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