Competition in the sodium iodide catalysed isomerisation of some aziridines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. The Isomerization of Some 1-Aroylaziridines. II
2. Hydrolysis of N-Methyl-2,4,4-substituted Δ2-Oxazolinium Iodides
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4. The Isomerization of Aziridine Derivatives
5. Intramolecular radical trapping in “set” ring opening of N-enoyl aziridines. A new mechanistic probe and a new synthesis of pyrrolidones.
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1. Conformational-dependent reaction mechanism: case of acid hydrolysis of N-benzoyl-9-azabicyclo[6.1.0]non-4-ene;Canadian Journal of Chemistry;2017-01
2. Experimental and theoretical rearrangement of N-acyl-2,2- dimethylaziridines in acidic medium;Journal of Chemical Sciences;2016-01-23
3. Regio-controlled and Stereo-controlled Ring Expansion ofN-Substituted-2 Benzoylaziridines Using Fe(NO3)3;Journal of Heterocyclic Chemistry;2014-05-05
4. Regio- and stereo-controlled isomerization of 1,2-diaroyl-3-aryl aziridines to the corresponding N-((Z)-1-oxo-1,3-diphenylprop-2-en-2-yl) benzamide;Journal of the Iranian Chemical Society;2014-02-01
5. Theoretical investigations on the mechanistic pathway of the thermal rearrangement of substituted N-acyl-2,2-dimethylaziridines;Journal of Molecular Modeling;2013-08-25
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