Chiral synthesis of the key intermediate for 1β-methylcarbapenem antibiotics starting from (–)-carvone
- 1 January 1991
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 12,p. 3027-3032
- https://doi.org/10.1039/p19910003027
Abstract
A stereoselective synthesis of the key intermediate for the preparation of 1β-methylcarbapenem antibiotics was achieved by using a cyclopentanone derivative, easily derived from (–)-carvone, as a starting material.Keywords
This publication has 9 references indexed in Scilit:
- An Enantioselective Synthesis of the Key Intermediate for the Preparation of 1b-Methylcarbapenem AntibioticsHETEROCYCLES, 1990
- Synthesis of the 1.BETA.-methylcarbapenem key intermediates.Journal of Synthetic Organic Chemistry, Japan, 1989
- Efficient chiral synthesis of Melillo's lactone, a key intermediate for the synthesis of thienamycinJournal of the Chemical Society, Chemical Communications, 1989
- A versatile synthesis of carbapenems from substituted dihydropyransTetrahedron Letters, 1988
- A novel Diels-Alder approach to carbapenemsTetrahedron Letters, 1988
- A stereoselective approach to 1β-methylcarbapenem antibiotic starting from ()-(−)-3-hydroxybutyric acid esterTetrahedron Letters, 1987
- Synthetic Carbapenem Antibiotics. I. 1-b-MethylcarbapenemHETEROCYCLES, 1984
- A practical synthesis of (±)-thienamycinTetrahedron Letters, 1980
- Diphenylphosphoryl azide. New convenient reagent for a modified Curtius reaction and for peptide synthesisJournal of the American Chemical Society, 1972