Stereoselective syntheses of quaternary substituted α-amino acids using oxazol-5-(4H)-ones
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference61 articles.
1. Design of Folded Peptides
2. Recent progress on the stereoselective synthesis of acyclic quaternary α-amino acids
3. Stereoselective synthesis of quaternary α-amino acids. Part 1: Acyclic compounds
4. Stereoselective synthesis of quaternary α-amino acids. Part 2: Cyclic compounds
5. Enantio‐ and Diastereoselective Construction of α,α‐Disubstituted α‐Amino Acids for the Synthesis of Biologically Active Compounds
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1. Enantioselective Construction of Consecutive Tetrasubstituted Stereogenic Centers by Reaction of α-Substituted β-Nitroacrylates with Oxazol-5-(4H)-ones Catalyzed by Cinchona Alkaloid Sulfonamide Catalysts;Organic Letters;2023-04-17
2. Highly diastereo- and enantioselective C2 addition of 5H-oxazol-4-ones to γ-keto-α,β-unsaturated esters;Chemical Communications;2023
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