Enantioselective Gold(I)-Catalyzed Hydrative Cyclizations of N-Propargyl-ynamides into 3,6-Dihydropyridinones

dc.contributor.author Febvay, Julie
dc.contributor.author Sanogo, Youssouf
dc.contributor.author Retailleau, Pascal
dc.contributor.author Gogoi, Manash Protim
dc.contributor.author Sahoo, Akhila K.
dc.contributor.author Marinetti, Angela
dc.contributor.author Voituriez, Arnaud
dc.date.accessioned 2022-03-27T09:44:17Z
dc.date.available 2022-03-27T09:44:17Z
dc.date.issued 2019-12-06
dc.description.abstract This study discloses the first enantioselective variant of the gold(I)-catalyzed hydrative cyclizations of ynamides, which have been implemented by using bis-gold(I) complexes of chiral diphosphines. Starting from N-propargyl-ynamides and water in the presence of p-toluenesulfonic acid, the cyclization reactions afford N-tosyl-3,6-dihydropyridin-2(1H)-ones in good isolated yields and with high levels of stereocontrol (20 examples, enantiomeric ratios up to 94:6).
dc.identifier.citation Organic Letters. v.21(23)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/acs.orglett.9b02644
dc.identifier.uri https://pubs.acs.org/doi/10.1021/acs.orglett.9b02644
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13252
dc.title Enantioselective Gold(I)-Catalyzed Hydrative Cyclizations of N-Propargyl-ynamides into 3,6-Dihydropyridinones
dc.type Journal. Article
dspace.entity.type
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