Gold-Catalyzed syn-1,2-Difunctionalization of Ynamides via Nitrile Activation

dc.contributor.author Vanjari, Rajeshwer
dc.contributor.author Dutta, Shubham
dc.contributor.author Gogoi, Manash P.
dc.contributor.author Gandon, Vincent
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T09:48:05Z
dc.date.available 2022-03-27T09:48:05Z
dc.date.issued 2018-12-21
dc.description.abstract Developed is an unprecedented Au(I)-catalyzed syn-1,2-difunctionalization of ynamides with 2-aminobenzonitriles via nitrile activation. The coupling between ynamides and 2-aminobenzonitriles is explicitly regioselective, providing a straightforward access to 2,4-diamino-substituted quinolines. Density functional theory (DFT) study provides insightful information and rationalizes the reaction pathway. It shows how the synergy between ynamide π-activation and nitrile σ-coordination by the Au(I) catalyst makes the cyclization viable.
dc.identifier.citation Organic Letters. v.20(24)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/acs.orglett.8b03830
dc.identifier.uri https://pubs.acs.org/doi/10.1021/acs.orglett.8b03830
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13319
dc.title Gold-Catalyzed syn-1,2-Difunctionalization of Ynamides via Nitrile Activation
dc.type Journal. Article
dspace.entity.type
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