Straightforward and Stereoselective Synthesis of α,β-Diamino Acid Derivatives by Means of an Organocatalyzed Decarboxylative Mannich Reaction
Author:
Affiliation:
1. Normandie Univ.; LCMT, ENSICAEN, UNICAEN, CNRS; 6 Boulevard du Maréchal Juin 14000 Caen France
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference45 articles.
1. α,β-Diamino Acids: Biological Significance and Synthetic Approaches
2. Catalytic asymmetric direct Mannich reaction: a powerful tool for the synthesis of α,β-diamino acids
3. Update 1 of: α,β-Diamino Acids: Biological Significance and Synthetic Approaches
4. The co-occurrence of two diastereoisomers of 2,3-diaminobutanoic acid in root nodule hydrolysates of Lotus tenuis
5. Identification of a novel β-replacement reaction in the biosynthesis of 2,3-diaminobutyric acid in peptidylnucleoside mureidomycin A
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1. Organocatalysis for Enantioselective Decarboxylative Nucleophilic Addition Reactions;European Journal of Organic Chemistry;2024-08-19
2. Organocatalytic Stereoselective Decarboxylative Addition of α‐Amido Malonic Acid Half Oxyesters to Isatins;Advanced Synthesis & Catalysis;2024-01-16
3. Decarboxylative Mannich Reactions with N‐Alkyl Imines;European Journal of Organic Chemistry;2023-04-19
4. Construction of α,β-Diamino Diacid Derivatives with Adjacent Acyclic Tetrasubstituted Stereocenters;The Journal of Organic Chemistry;2022-06-17
5. Substituted Malonic Acid Half Oxyesters (SMAHOs): Green Nucleophiles for Organic Synthesis;European Journal of Organic Chemistry;2022-02
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