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CC BY-ND-NC 4.0 · SynOpen 2017; 01(01): 0015-0023
DOI: 10.1055/s-0036-1588809
DOI: 10.1055/s-0036-1588809
paper
A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines
Further Information
Publication History
Received: 02 March 2017
Accepted after revision: 09 April 2017
Publication Date:
25 April 2017 (online)
Abstract
We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an effective reagent in the presence of NH2OH·HCl and NaIO4. We found that the same combination of NH2OH·HCl and NaIO4 is also very effective for nucleophilic ring opening of aziridines.
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For mitomycins, see:
For azinomycins, see:
For maduropeptin, see:
For ficellomycin, see:
For miraziridine, see:
For azicemicins, see: