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dc.contributor.authorGómez San Juan, Asier
dc.contributor.authorSotomayor Anduiza, María Nuria
dc.contributor.authorLete Expósito, María Esther
dc.date.accessioned2014-02-03T15:20:52Z
dc.date.available2014-02-03T15:20:52Z
dc.date.issued2013-02
dc.identifier.citationBeilstein Journal of Organic Chemistry 9 : 313-322 (2013)es
dc.identifier.issn1860-5397
dc.identifier.urihttp://hdl.handle.net/10810/11329
dc.description.abstractIn this review we summarize recent developments in inter- and intramolecular enantioselective carbolithiation reactions carried out in the presence of a chiral ligand for lithium, such as (-)-sparteine, to promote facial selection on a C=C bond. This is an attractive approach for the construction of new carbon-carbon bonds in an asymmetric fashion, with the possibility of introducing further functionalization on the molecule by trapping the reactive organolithium intermediates with electrophiles.es
dc.description.sponsorshipMinisterio de Ciencia e Innovacion (CTQ2009-07733) and Universidad del Pais Vasco/Euskal Herriko Unibertsitatea (UFI11/22, GIU 0946) for their financial support. Technical and personnel support provided by Servicios Generales de Investigacion SGIker (UPV/EHU, MICINN, GV/EJ, ERDF and ESF) is gratefully acknowledged. We also thank UPV/EHU for a postdoctoral grant (A.G).es
dc.language.isoenges
dc.publisherBeilstein Institutes
dc.relationinfo:eu-repo/grantAgreement/MICINN/CTQ2009-07733
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectalkeneses
dc.subjectasymmetric synthesises
dc.subjectcarbolithiationes
dc.subjectcarbometallationes
dc.subjectenantioselectivityes
dc.subjectlithiumes
dc.titleInter- and intramolecular enantioselective carbolithiation reactionses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2013 Gómez-SanJuan et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)es
dc.relation.publisherversionhttp://www.beilstein-journals.org/bjoc/single/articleFullText.htm?publicId=1860-5397-9-36es
dc.identifier.doi10.3762/bjoc.9.36
dc.departamentoesQuímica orgánica IIes_ES
dc.departamentoeuKimika organikoa IIes_ES
dc.subject.categoriaCHEMISTRY, ORGANIC


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