Asymmetric nucleophilic substitution of α-bromo amides via dynamic kinetic resolution for the preparation of dipeptide analogues
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Dynamic kinetic resolution (DKR) using immobilized amine nucleophiles
2. Dynamic thermodynamic resolution of N-methylpseudoephedrine α-bromo esters for asymmetric syntheses of α-hydroxy carboxylic acid derivatives
3. Asymmetric syntheses of α-mercapto carboxylic acid derivatives by dynamic resolution of N-methyl pseudoephedrine α-bromo esters
4. Dynamic Resolution of α-Bromo-α-Alkyl Esters Using N-Methyl Pseudo-ephedrine as a Chiral Auxiliary: Asymmetric Syntheses of α-Amino Acid Derivatives
5. Synthesis of α-amino esters by dynamic kinetic resolution of α-haloacyl imidazolidinones
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3. Dual Enantioselective Control using D-phenylglycine-L-proline-derived Catalysts for the Enantioselective Addition of Diethylzinc to Aldehyde;Bulletin of the Korean Chemical Society;2015-12-21
4. Asymmetric Synthesis of 3,4,6-Trisubstituted 2,5-Diketopiperazines by Using Dynamic Kinetic Resolution of α-Bromo Tertiary Acetamides;European Journal of Organic Chemistry;2014-03-06
5. Kinetic Resolution-Related PROCESSES;Key Chiral Auxiliary Applications;2014
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