An Enantioselective Synthesis of the Key Intermediate for the Preparation of 1b-Methylcarbapenem Antibiotics
- 1 January 1990
- journal article
- research article
- Published by CLOCKSS Archive in HETEROCYCLES
- Vol. 31 (7) , 1225-1228
- https://doi.org/10.3987/com-90-5435
Abstract
An enantioselective synthesis of the key intermediate for the preparation of 1.beta.-methylcarbapenem has been achieved by employing the cyclopentane derivative (8), as a chiral source, readily derived from (-)-carvone.Keywords
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