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Organocatalytic Enantioselective Aminoalkylation of 5-Aminopyrazole Derivatives with Cyclic Imines

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Organocatalytic Enantioselective Aminoalkylation of 5-Aminopyrazole Derivatives with Cyclic Imines

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dc.contributor.author Carceller-Ferrer, Laura
dc.contributor.author González del Campo, Aleix
dc.contributor.author Vila Descals, Carlos
dc.contributor.author Blay Llinares, Gonzalo
dc.contributor.author Muñoz, M. Carmen
dc.contributor.author Pedro, José Ramón
dc.date.accessioned 2022-11-29T15:08:56Z
dc.date.available 2022-11-29T15:08:56Z
dc.date.issued 2020
dc.identifier.citation Carceller-Ferrer, Laura González del Campo, Aleix Vila Descals, Carlos Blay Llinares, Gonzalo Muñoz, M. Carmen Pedro, José Ramón 2020 Organocatalytic Enantioselective Aminoalkylation of 5-Aminopyrazole Derivatives with Cyclic Imines European Journal of Organic Chemistry 2020 48 7450 7454
dc.identifier.uri https://hdl.handle.net/10550/84623
dc.description.abstract The first enantioselective alkylation of 5‐aminopyrazoles is described with good results. The organocatalytic alkylation of 5‐aminopyrazoles have been accomplished using benzoxathiazine 2,2‐dioxides as electrophiles and a bifunctional squaramide organocatalyst.
dc.language.iso eng
dc.relation.ispartof European Journal of Organic Chemistry, 2020, vol. 2020, num. 48, p. 7450-7454
dc.subject Química orgànica
dc.subject Catàlisi
dc.title Organocatalytic Enantioselective Aminoalkylation of 5-Aminopyrazole Derivatives with Cyclic Imines
dc.type journal article es_ES
dc.date.updated 2022-11-29T15:08:56Z
dc.identifier.doi 10.1002/ejoc.202001314
dc.identifier.idgrec 142281
dc.rights.accessRights open access es_ES

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