Towards taxane analogues synthesis by dienyne ring closing metathesis

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dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Molecularesgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
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.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 taxolgl
dc.description.peerreviewedNONgl
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 networkgl
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/C6QO00321Dgl
dc.identifier.doi10.1039/C6QO00321D
dc.identifier.essn2052-4129
dc.identifier.urihttp://hdl.handle.net/10347/17005
dc.language.isoenggl
dc.publisherRoyal Society of Chemistrygl
dc.relation.publisherversionhttps://doi.org/10.1039/C6QO00321Dgl
dc.rights© The Royal Society of Chemistry 2016gl
dc.rights.accessRightsopen accessgl
dc.subjectTaxanegl
dc.subjectRing closing metathesisgl
dc.subject.classificationMaterias::Investigación::23 Química::2306 Química orgánicagl
dc.titleTowards taxane analogues synthesis by dienyne ring closing metathesisgl
dc.typejournal articlegl
dc.type.hasVersionSMURgl
dspace.entity.typePublication
relation.isAuthorOfPublicationfb6bbc55-1505-4e96-9863-825f7d16309c
relation.isAuthorOfPublication.latestForDiscoveryfb6bbc55-1505-4e96-9863-825f7d16309c

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