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dc.contributor.authorPertejo Fernández, Pablo
dc.contributor.authorGonzález Saiz, Beatriz 
dc.contributor.authorQuesada Pato, Roberto 
dc.contributor.authorGarcía Valverde, María 
dc.date.accessioned2021-03-16T09:06:09Z
dc.date.available2021-03-16T09:06:09Z
dc.date.issued2020-11
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/10259/5648
dc.description.abstractA simple one-pot protocol for the synthesis of fused pyrrolopiperazines with a complete diastereoselectivity has been developed. This novel methodology combined the Ugi reaction with a spontaneous enamine alkylation on a multicomponent domino reaction, starting from nonprotected diamines and arylglyoxals.en
dc.description.sponsorshipConsejerıá de Educacioń de la Junta de Castilla y León (project BU075G19)es
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherAmerican Chemical Societyes
dc.relation.ispartofThe Journal of Organic Chemistry. 2020, V. 85, n. 21, p. 14240–14245es
dc.subject.otherQuímica orgánicaes
dc.subject.otherChemistry, Organicen
dc.titleOne-Pot Synthesis of Enantiopure Pyrrolopiperazinesen
dc.typeinfo:eu-repo/semantics/article
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.relation.publisherversionhttps://doi.org/10.1021/acs.joc.0c02103
dc.identifier.doi10.1021/acs.joc.0c02103
dc.relation.projectIDinfo:eu-repo/grantAgreement/JCyL/BU075G19
dc.identifier.essn1520-6904
dc.journal.titleThe Journal of Organic Chemistryes
dc.volume.number85es
dc.issue.number21es
dc.page.initial14240es
dc.page.final14245es
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersion


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