Regioselective electrophilic substitution of 2,3-aziridino-γ-lactones: preliminary studies aimed at the synthesis of α,α-disubstituted α- or β-amino acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 articles.
1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
2. Aziridines: epoxides’ ugly cousins?
3. Recent Synthetic Applications of Chiral Aziridines
4. Enantio‐ and Diastereoselective Construction of α,α‐Disubstituted α‐Amino Acids for the Synthesis of Biologically Active Compounds
5. Recent approaches towards the asymmetric synthesis of α,α-disubstituted α-amino acids
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1. Aziridines and Azirines: Fused-Ring Derivatives;Comprehensive Heterocyclic Chemistry IV;2022
2. Furan‐Derived Chiral Bicycloaziridino Lactone Synthon: Collective Syntheses of Oseltamivir Phosphate (Tamiflu), ( S )‐Pipecolic acid and its 3‐Hydroxy Derivatives;Chemistry – An Asian Journal;2020-01-20
3. D-Ribonolactone, A Versatile Synthetic Precursor of Biologically Relevant Scaffolds;Current Organic Synthesis;2015-08-21
4. Stereoselective synthesis of C-sulfonylated aziridines from halomethyl phenyl sulfone and N-tert-butanesulfinyl imines;RSC Adv.;2014
5. Synthesis of enantiomerically pure model compounds of the glucose-6-phosphate-T1-translocase inhibitors kodaistatins A–D. Inferences with regard to the stereostructure of the natural products;Tetrahedron;2013-09
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