Lithium perchlorate-catalyzed regioselective ring-opening of aziridines with potassium thiocyanate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
2. Recent Synthetic Applications of Chiral Aziridines
3. Nucleophilic opening of chiral bis(aziridines): a route to enantiomerically pure .alpha.-amino aldehydes or acids and polysubstituted piperidines
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1. Ring-opening and cyclization of aziridines with aryl azides: metal-free synthesis of 6-(triflyloxy)quinolines;Organic Chemistry Frontiers;2018
2. Recent advances in the transformations of cycloalkane-fused oxiranes and aziridines;Tetrahedron;2017-09
3. Asymmetric Synthesis of 2-Thiocyanato-2-(1-aminoalkyl)-substituted 1-Tetralones and 1-Indanones with Tetrasubstituted Carbon Stereogenic Centers via Cooperative Cation-Binding Catalysis;Advanced Synthesis & Catalysis;2017-04-28
4. Bimetallic catalysis in the highly enantioselective ring–opening reactions of aziridines;Chem. Sci.;2014
5. Studies on the true catalyst in the phosphate-promoted desymmetrization of meso-aziridines with silylated nucleophiles;Tetrahedron;2013-01
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