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

No Thumbnail Available
Date
2019-12-13
Authors
Naveen, Naganaboina
Ramesh, Golla
Balamurugan, Rengarajan
Journal Title
Journal ISSN
Volume Title
Publisher
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.
Description
Keywords
AgSbF 6, Meyer-Schuster rearrangement, Tertiary propargyl alcohols, α -iodoenones, α,β-unsaturated enones
Citation
ChemistrySelect. v.4(46)