Regioselective ring opening of aziridines with activated DMF complexes: a facile synthesis of β-haloamines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
2. Nucleophilic opening of chiral bis(aziridines): a route to enantiomerically pure .alpha.-amino aldehydes or acids and polysubstituted piperidines
3. Enantioselective routes toward 1β-methylcarbapenems from chiral aziridines
4. Microbial oxidation of chloroaromatics in the enantiodivergent synthesis of pyrrolizidine alkaloids: trihydroxyheliotridanes
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1. Aziridine synthesis by ring-closure of haloimines;Synthesis of Aziridines and Oxaziridines from Imines;2024
2. Use of allylzinc halide as a source of halide: Differential addition of nucleophiles to Ts-aziridines and aldehydes under similar reaction conditions;Tetrahedron Letters;2019-01
3. Regioselective Ring-Opening Reactions of Unsymmetric Azetidines;PROG CHEM;2017
4. Stereoselective synthesis of erythro-β-chloroamines and their conversion into functionalized trans-oxazolidin-2-ones;Tetrahedron;2014-08
5. Highly efficient regioselective ring openings of N-tosylaziridines to haloamines using ferric (III) halides;Chinese Chemical Letters;2014-08
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