A New Synthesis of γ-Butyrolactones via AuCl3 or Hg (II)-Catalyzed Intramolecular Hydroalkoxylation of 4-Bromo-3-yn-1-ols†

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dc.contributor.author Reddy, M S
dc.contributor.author Kumar, Y K
dc.contributor.author Thirupathi, Nuligonda
dc.date.accessioned 2012-05-24T04:42:20Z
dc.date.available 2012-05-24T04:42:20Z
dc.date.issued 2012
dc.identifier.citation Organic Letters 2012, 14 (3), 824–827 en
dc.identifier.uri http://hdl.handle.net/123456789/761
dc.description.abstract The article describes an efficient conversion of 4-bromo-3-yn-1-ols to γ-butyrolactones via AuCl3 catalyzed electrophilic cyclization (hydroxyl assisted regioselective hydration) in wet toluene. Various 2o and 3o alcohols including benzylic systems were found to be equally reactive with moderate to excellent yields obtained in all cases. en
dc.format.extent 220624 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CDRI Communication No. 8192 en
dc.subject γ-butyrolactones en
dc.subject electrophilic cyclization en
dc.subject benzylic en
dc.title A New Synthesis of γ-Butyrolactones via AuCl3 or Hg (II)-Catalyzed Intramolecular Hydroalkoxylation of 4-Bromo-3-yn-1-ols† en
dc.type Article en


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