Catalytic Enantioselective Addition of Me2Zn to Isatins
NAGIOS: RODERIC FUNCIONANDO

Catalytic Enantioselective Addition of Me2Zn to Isatins

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Catalytic Enantioselective Addition of Me2Zn to Isatins

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dc.contributor.author Vila Descals, Carlos
dc.contributor.author Del Campo, Andrés
dc.contributor.author Blay Llinares, Gonzalo
dc.contributor.author Pedro, José Ramón
dc.date.accessioned 2019-11-11T15:17:00Z
dc.date.available 2019-11-11T15:17:00Z
dc.date.issued 2017
dc.identifier.uri https://hdl.handle.net/10550/72167
dc.description.abstract Chiral α-hydroxyamide L5 derived from (S)-(+)-mandelic acid catalyzes the enantioselective addition of dimethylzinc to isatins affording the corresponding chiral 3-hydroxy-3-methyl-2-oxindoles with good yields and er up to 90:10. Furthermore, several chemical transformations were performed with the 3-hydroxy-2-oxindoles obtained.
dc.language.iso eng
dc.relation.ispartof Catalysts, 2017, vol. 7, num. 12, p. 387
dc.rights.uri info:eu-repo/semantics/openAccess
dc.source Vila Descals, Carlos Del Campo, Andrés Blay Llinares, Gonzalo Pedro, José Ramón 2017 Catalytic Enantioselective Addition of Me2Zn to Isatins Catalysts 7 12 387
dc.subject Química orgànica
dc.subject Catàlisi
dc.title Catalytic Enantioselective Addition of Me2Zn to Isatins
dc.type info:eu-repo/semantics/article
dc.date.updated 2019-11-11T15:17:00Z
dc.identifier.doi https://doi.org/10.3390/catal7120387
dc.identifier.idgrec 121636

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