Silver-Catalyzed Synthesis of Enones/α-Iodoenones from Tertiary Propargyl Alcohols

dc.contributor.author Naveen, Naganaboina
dc.contributor.author Ramesh, Golla
dc.contributor.author Balamurugan, Rengarajan
dc.date.accessioned 2022-03-27T08:38:55Z
dc.date.available 2022-03-27T08:38:55Z
dc.date.issued 2019-12-13
dc.description.abstract Tertiary propargyl alcohols undergo smooth Meyer-Schuster rearrangement to give enones in the presence of silver catalyst alone at room temperature. The intermediate can be trapped using NIS to make useful tetra substituted α-iodoenones.
dc.identifier.citation ChemistrySelect. v.4(46)
dc.identifier.uri 10.1002/slct.201903568
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/slct.201903568
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11355
dc.subject AgSbF 6
dc.subject Meyer-Schuster rearrangement
dc.subject Tertiary propargyl alcohols
dc.subject α -iodoenones
dc.subject α,β-unsaturated enones
dc.title Silver-Catalyzed Synthesis of Enones/α-Iodoenones from Tertiary Propargyl Alcohols
dc.type Journal. Article
dspace.entity.type
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