HIGHLY STEREOSELECTIVE ALDOL-TYPE REACTION OF CHIRAL TIN(II) ENOLATE. FORMAL TOTAL SYNTHESIS OF (±)-THIENAMYCIN
- 5 April 1986
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 15 (4) , 637-640
- https://doi.org/10.1246/cl.1986.637
Abstract
Highly efficient internal chiral induction is achieved in the aldol-type reaction of tin(II) enolate generated from 3-amino-substituted butanoylthiazolidine-2-thione. This reaction is successfully applied to the formal total synthesis of (±)-thienamycin.Keywords
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- A CONVENIENT METHOD FOR THE CONSTRUCTION OF β-LACTAM COMPOUNDS FROM β-AMINO ACIDS USING 2-CHLORO-1-METHYLPYRIDINIUM IODIDE AS CONDENSING REAGENTChemistry Letters, 1984