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dc.contributor.authorPérez-Estrada, S.
dc.contributor.authorSayar, N.
dc.contributor.authorGranja Guillán, Juan Ramón
dc.date.accessioned2018-07-10T07:40:51Z
dc.date.available2018-07-10T07:40:51Z
dc.date.issued2016-10-01
dc.identifier.citationPérez-Estrada, S.,Sayar, N. & Granja, J. (2017). Towards taxane analogues synthesis by dienyne ring closing metathesis . Org. Chem. Front., 2016,3, 1331-1336 . http://dx.doi.org/10.1039/C6QO00321D
dc.identifier.urihttp://hdl.handle.net/10347/17005
dc.description.abstractHerein we report the facile construction of taxadiene analogues by ring closing metathesis of dienynes built on a cyclohexenone with a natural configuration at C1 and its further transformation to incorporate most of the key functional groups of taxol
dc.description.sponsorshipThis work was supported by the Spanish Ministry of Economy and Competitivity (Mineco) and the ERDF (CTQ2010‐15725, CTQ2013‐43264‐R and CTQ2014‐51912‐REDC), and by the Xunta de Galicia and the ERDF (GPC2013‐039, EM2012/117 and EM2014/011). N. S. thanks Mineco for his FPU contract and S. P.‐E. to the CONACYT for his fellowship (No. 162219). We also thank ORFEO‐CINCA network
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.rights© The Royal Society of Chemistry 2016
dc.subjectTaxane
dc.subjectRing closing metathesis
dc.subject.classificationMaterias::Investigación::23 Química::2306 Química orgánica
dc.titleTowards taxane analogues synthesis by dienyne ring closing metathesis
dc.typeinfo:eu-repo/semantics/article
dc.identifier.DOI10.1039/C6QO00321D
dc.relation.publisherversionhttps://doi.org/10.1039/C6QO00321D
dc.type.versioninfo:eu-repo/semantics/submittedVersion
dc.identifier.e-issn2052-4129
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánica
dc.description.peerreviewedNON


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