1. The asymmetric halogenation of chiral imide enolates

a general approach to the synthesis of enantiomerically pure α-amino acids ; 2. Regioselective carboximide hydrolysis with lithium hydroperoxide ; 3. The total synthesis of the isodityrosine-derived cyclic tripeptides OF4949-III and K-13 ; 4. An oxidative macrocyclization approach to vancomycin

By Jonathan A. Ellman

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Publish Date

1989

Publisher

Language

eng

Pages

244

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1. The asymmetric halogenation of chiral imide enolates

1. The asymmetric halogenation of chiral imide enolatesa general approach to the synthesis of enantiomerically pure α-amino acids ; 2. Regioselective carboximide hydrolysis with lithium hydroperoxide ; 3. The total synthesis of the isodityrosine-derived cyclic tripeptides OF4949-III and K-13 ; 4. An oxidative macrocyclization approach to vancomycin

Language: eng

Pages: 244

Published In: 1989