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dc.contributor.authorBarravecchia Prado, Liliana Inés
dc.contributor.authorNeira García, Iago
dc.contributor.authorPazos Chantrero, Elena
dc.contributor.authorPeinador Veira, Carlos
dc.contributor.authorGarcía Romero, Marcos Daniel
dc.date.accessioned2025-02-18T11:35:20Z
dc.date.available2025-02-18T11:35:20Z
dc.date.issued2022
dc.identifier.issn1520-6904
dc.identifier.urihttp://hdl.handle.net/20.500.11940/19545
dc.description.abstractWe present herein the development of a series of viologen–amino acid hybrids, obtained in good yields either by successive alkylations of 4,4′-bipyridine, or by Zincke reactions followed by a second alkylation step. The potential of the obtained amino acids has been exemplified, either as typical guests of the curcubituril family of hosts (particularly CB[7]/[8]) or as suitable building blocks for the solution/solid-phase synthesis of two model tripeptides with the viologen core inserted within their sequences.
dc.language.isoenes
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleAmino Acid–Viologen Hybrids: Synthesis, Cucurbituril Host–Guest Chemistry, and Implementation on the Production of Peptides
dc.typeJournal Articlees
dcterms.bibliographicCitationBarravecchia L, Neira I, Pazos E, Peinador C, García MD. Amino Acid–Viologen Hybrids: Synthesis, Cucurbituril Host–Guest Chemistry, and Implementation on the Production of Peptides. Journal of Organic Chemistry. 2022;87(1):760-4.
dc.authorsophosBarravecchia, M. D. L.;Neira, I.;Pazos, E.;Peinador, C.;García
dc.identifier.doi10.1021/ACS.JOC.1C02040
dc.identifier.sophos61ff06bc13638e1cfc277b71
dc.issue.number1
dc.journal.titleJournal of Organic Chemistry
dc.page.initial760
dc.page.final764
dc.relation.publisherversionhttps://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02040es
dc.rights.accessRightsopenAccess
dc.subject.keywordINIBICes
dc.volume.number87


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