Catalytic Enantioselective Synthesis of a-aryl a-hydrazino Esters and Amides

Velázquez Muñoz, Marta; Alberca Manzano, Saúl; Iglesias Sigüenza, Francisco Javier; Fernández Fernández, Rosario Fátima; Lassaletta, José M; Monge Fernández, David

doi:10.1039/d0cc02478c

Artículo

dc.creator	Velázquez Muñoz, Marta	es
dc.creator	Alberca Manzano, Saúl	es
dc.creator	Iglesias Sigüenza, Francisco Javier	es
dc.creator	Fernández Fernández, Rosario Fátima	es
dc.creator	Lassaletta, José M	es
dc.creator	Monge Fernández, David	es
dc.date.accessioned	2022-11-29T15:01:32Z
dc.date.available	2022-11-29T15:01:32Z
dc.date.issued	2020
dc.identifier.citation	Velázquez Muñoz, M., Alberca Manzano, S., Iglesias Sigüenza, F.J., Fernández Fernández, R.F., Lassaletta, J.M. y Monge Fernández, D. (2020). Catalytic Enantioselective Synthesis of a-aryl a-hydrazino Esters and Amides. Chemical Communications, 56 (43), 5823-5826. https://doi.org/10.1039/d0cc02478c.
dc.identifier.issn	1359-7345	es
dc.identifier.issn	1364-548X	es
dc.identifier.uri	https://hdl.handle.net/11441/139898
dc.description.abstract	Catalysts generated by combinations of Pd(TFA)2and pyridine-hydrazone ligands have allowed the asymmetric 1,2-addition of aryl boronic acids toN-carbamoyl (Cbz and Fmoc) protected glyoxylate-derived hydrazones, yielding a-aryl a-hydrazino esters/amides in high enantioselectivities. Subsequent removal of the carbamoyl moiety affords key building blocks en route to hydrazinopeptides,N-aminopeptides and peptidomimetics thereof.	es
dc.format	application/pdf	es
dc.format.extent	5 p.	es
dc.language.iso	eng	es
dc.publisher	Royal Society of Chemistry	es
dc.relation.ispartof	Chemical Communications, 56 (43), 5823-5826.
dc.rights	Attribution-NonCommercial-NoDerivatives 4.0 Internacional	*
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/4.0/	*
dc.title	Catalytic Enantioselective Synthesis of a-aryl a-hydrazino Esters and Amides	es
dc.type	info:eu-repo/semantics/article	es
dcterms.identifier	https://ror.org/03yxnpp24
dc.type.version	info:eu-repo/semantics/acceptedVersion	es
dc.rights.accessRights	info:eu-repo/semantics/openAccess	es
dc.contributor.affiliation	Universidad de Sevilla. Departamento de Química orgánica	es
dc.relation.publisherversion	https://dx.doi.org/10.1039/d0cc02478c	es
dc.identifier.doi	10.1039/d0cc02478c	es
dc.journaltitle	Chemical Communications	es
dc.publication.volumen	56	es
dc.publication.issue	43	es
dc.publication.initialPage	5823	es
dc.publication.endPage	5826	es

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