Efficient chiral synthesis of Melillo's lactone, a key intermediate for the synthesis of thienamycin
- 1 January 1989
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 10,p. 646-647
- https://doi.org/10.1039/c39890000646
Abstract
Optically active Melillo's lactone (13) was synthesised from the cyclopentane derivative (7), easily derived from (–)-carvone.Keywords
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