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  • A new synthesis of γ-butyrolactones via AuCl(3)- or Hg(II)-catalyzed intramolecular hydroalkoxylation of 4-bromo-3-yn-1-ols.

A new synthesis of γ-butyrolactones via AuCl(3)- or Hg(II)-catalyzed intramolecular hydroalkoxylation of 4-bromo-3-yn-1-ols.

Organic letters (2012-01-27)
Maddi Sridhar Reddy, Yalla Kiran Kumar, Nuligonda Thirupathi
ZUSAMMENFASSUNG

An efficient conversion of 4-bromo-3-yn-1-ols to γ-butyrolactones via AuCl(3)-catalyzed electrophilic cyclization (hydroxyl-assisted regioselective hydration) in wet toluene is described. Various secondary and tertiary alcohols including benzylic systems were found to be equally reactive with moderate to excellent yields obtained in all cases.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Gold(III)-chlorid, 99%
Sigma-Aldrich
Gold(III)-chlorid, ≥99.99% trace metals basis
Sigma-Aldrich
Gold(I)-chlorid, 99.9% trace metals basis