Synthesis of α-amino acids by ring opening of aziridine-2-carboxylates with carbon nucleophiles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
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2. Synthesis of N-substituted aziridine-2-carboxylates
3. Synthesis ofthreo-3-Methylcysteine from Threonine
4. Studies on 2-Aziridinecarboxylic Acid. IX. Convenient Synthesis of Optically ActiveS-Alkylcysteine,threo-S-Alkyl-β-methylcysteine, and Lanthionine Derivativesviathe Ring-opening Reaction of Aziridine by Several Thiols
5. Determination of the absolute configuration of (−)-S-(2-carboxypropyl)-L-cysteine
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3. Asymmetric Synthesis of β 2 ‐Aryl Amino Acids through Pd‐Catalyzed Enantiospecific and Regioselective Ring‐Opening Suzuki–Miyaura Arylation of Aziridine‐2‐carboxylates;Chemistry – A European Journal;2019-07-08
4. Formation of Amines from Other Amines and Derivatives;Comprehensive Organic Transformations;2018-02-28
5. Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey–Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters;Organic Letters;2015-11-11
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