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Synthesis of trans‐β‐Elemene
dc.contributor.authorBenito Iglesias, David
dc.contributor.authorHerrero Teijón, Pablo 
dc.contributor.authorRubio González, María Rosa 
dc.contributor.authorFernández Mateos, Alfonso
dc.date.accessioned2024-01-15T12:00:15Z
dc.date.available2024-01-15T12:00:15Z
dc.date.issued2018
dc.identifier.citationBenito Iglesias, D., Herrero Teijón, P., Rubio González, R. & Fernández Mateos, A. (2018). Synthesis of trans‐β‐Elemene. European Journal of Organic Chemistry, 2018(35), 4926–4932. https://doi.org/10.1002/ejoc.201800800es_ES
dc.identifier.issn1434-193X
dc.identifier.urihttp://hdl.handle.net/10366/154243
dc.description.abstract[EN]Highly efficient syntheses of the anti-cancer agent trans-β-elemene have been achieved by using the readily available (±)-limonene as starting material. The syntheses were achieved in only nine to eleven steps with good overall yields. The key step in these reaction sequences is a stereoselective radical cyclization, induced by titanocene chloride.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectQuímica orgánicaes_ES
dc.subjectAnticancerososes_ES
dc.subjectRadicales (Química)es_ES
dc.subjectCloruroses_ES
dc.titleSynthesis of trans‐β‐Elemenees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1002/ejoc.201800800es_ES
dc.subject.unesco2306 Química Orgánicaes_ES
dc.identifier.doi10.1002/ejoc.201800800
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1099-0690
dc.journal.titleEuropean Journal of Organic Chemistryes_ES
dc.volume.number2018es_ES
dc.issue.number35es_ES
dc.page.initial4926es_ES
dc.page.final4932es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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