2-Carbamoylaziridine (Leakadine): diastereoselective transformations and stereoelectronic effect

Diastereoselective transformations of Leakadine were discovered: dimerization during melting or heating in CHCl 3 with the formation of one diastereomer. The obtained dimer reacts with methyl isocyanate under mild conditions with the formation of an N -methylcarbamoyl derivative – also in the form o...

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Veröffentlicht in:Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2012-09, Vol.48 (6), p.869-874
Hauptverfasser: Kostyanovsky, R. G., Kadorkina, G. K., Krutius, O. N., Chervin, I. I.
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Sprache:eng
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