Gold-catalyzed ethylene cyclopropanation

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dc.contributor.authorRull, Silvia G.
dc.contributor.authorOlmos Verge, Andrea
dc.contributor.authorPérez Romero, Pedro José
dc.date.accessioned2019-02-07T08:23:45Z
dc.date.available2019-02-07T08:23:45Z
dc.date.issued2019
dc.description.abstractEthylene can be directly converted into ethyl 1-cyclopropylcarboxylate upon reaction with ethyl diazoacetate (N2CHCO2Et, EDA) in the presence of catalytic amounts of IPrAuCl/NaBAr4F (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazole-2-ylidene, BAr4F = tetrakis(3,5-bis(trifluoromethyl)phenyl)borate).es_ES
dc.description.centerCIQSO
dc.description.departmentQuímica "Profesor José Carlos Vílchez Martín"
dc.description.sponsorshipSupport for this work was provided by the MINECO (CTQ2017-82893-C2-1-R and CTQ2015-73693-JIN)
dc.identifier.citationRull, S. G., Olmos, A., & Pérez, P. J. (2019). Gold-catalyzed ethylene cyclopropanation. Beilstein Journal of Organic Chemistry, 15, 67-71. https://doi.org/10.3762/bjoc.15.7es_ES
dc.identifier.doi10.3762/bjoc.15.7
dc.identifier.issn1860-5397
dc.identifier.urihttp://hdl.handle.net/10272/15934
dc.language.isoenges_ES
dc.publisherBeilstein-Institutes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO [TQ2017-82893-C2-1-R and CTQ2015-73693-JIN]
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.titleGold-catalyzed ethylene cyclopropanationes_ES
dc.typejournal articlees_ES
dspace.entity.typePublication
relation.isAuthorOfPublication1ff94984-3f6a-4c99-a44b-3b3858c3813f
relation.isAuthorOfPublicationc6f8222a-d8d2-4736-baa6-4a2330bdf6b6
relation.isAuthorOfPublication.latestForDiscovery1ff94984-3f6a-4c99-a44b-3b3858c3813f

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