A simple chiral synthesis of both (R)- and (S)-mevalonolactones from a single precursor via diastereocontrolled oxygenation
- 1 January 1984
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 2,p. 82-83
- https://doi.org/10.1039/c39840000082
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.Keywords
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