NAGIOS: RODERIC FUNCIONANDO

Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones

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dc.contributor.author	Monleón Ventura, Alicia
dc.contributor.author	Blay Llinares, Gonzalo
dc.contributor.author	Pedro, José Ramón
dc.date.accessioned	2022-06-13T12:58:39Z
dc.date.available	2022-06-13T12:58:39Z
dc.date.issued	2022
dc.identifier.uri	https://hdl.handle.net/10550/83111
dc.description.abstract	A convenient procedure of synthesis of N-carbamoyl-protected propargylic amines substituted with a cyclopropyl group from alpha-amido sulfones and cyclopropylacetylene is described. The reaction is catalyzed by a chiral BINOL-type zinc complex and provides the corresponding products in good yields and enantioselectivities.
dc.language.iso	eng
dc.relation.ispartof	Molecules, 2022, vol. 27, num. 12, p. 3763
dc.source	Monleón Ventura, Alicia Blay Llinares, Gonzalo Pedro, José Ramón 2022 Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones Molecules 27 12 3763
dc.subject	Catàlisi
dc.subject	Química orgànica
dc.title	Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones
dc.type	journal article	es_ES
dc.date.updated	2022-06-13T12:58:39Z
dc.identifier.doi	https://doi.org/10.3390/molecules27123763
dc.identifier.idgrec	154121
dc.rights.accessRights	open access	es_ES