Reaction of aziridinecar☐ylic acids with thiols in aqueous solution. the formation of β-amino acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. 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
2. THE STEREOSELECTIVE FORMATION OF THREONINE FROMcis- ANDtrans-1-α-METHYLBENZYL-2-METHOXYCARBONYL-3-METHYL AZIRIDINES
3. Réactivité des N-vinylaziridines fonctionnalisées. Synthèse de dérivés des α,β-déhydro α-amino acides
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1. Microwave Heating Promotes the S-Alkylation of Aziridine Catalyzed by Molecular Sieves: A Post-Synthetic Approach to Lanthionine-Containing Peptides;Molecules;2021-10-11
2. A facile and regioselective multicomponent synthesis of chiral aryl-1,2-mercaptoamines in water followed by monoamine oxidase (MAO-N) enzymatic resolution;Organic & Biomolecular Chemistry;2019
3. Progress in Lanthionine and Protected Lanthionine Synthesis;Chemistry – A European Journal;2018-08-02
4. Regio- and Stereospecific Synthesis of Oridonin D-Ring Aziridinated Analogues for the Treatment of Triple-Negative Breast Cancer via Mediated Irreversible Covalent Warheads;Journal of Medicinal Chemistry;2018-03-12
5. Formation of Amines from Other Amines and Derivatives;Comprehensive Organic Transformations;2018-02-28
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