Issue 2, 1984

A simple chiral synthesis of both (R)- and (S)-mevalonolactones from a single precursor via diastereocontrolled oxygenation

Abstract

A synthesis of (R)- and (S)-mevalonolactones (10) has been developed from the common chiral lactone precursor (1) by diastereocontrolled oxygenation with a molybdenum peroxide complex.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 82-83

A simple chiral synthesis of both (R)- and (S)-mevalonolactones from a single precursor via diastereocontrolled oxygenation

S. Takano, M. Morimoto and K. Ogasawara, J. Chem. Soc., Chem. Commun., 1984, 82 DOI: 10.1039/C39840000082

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