| Autor: |
Koehler, K. F., Zaddach, H., Kadorkina, G. K., Voznesenskii, V. N., Chervin, I. I., Kostyanovsky, R. G. |
| Zdroj: |
Russian Chemical Bulletin; December 1993, Vol. 42 Issue: 12 p2049-2052, 4p |
| Abstrakt: |
The structure of azimexone (3), the product of the reaction of 2-cyanoaziridine with acetone, was confirmed on the basis of1H and13C NMR spectra. The formation of this product is accounted for by the a-aziridinoalkylating action of an intermediate containing a good leaving iminoyloxy group. Similar reactions were observed for 1-chloromethylaziridine and a 1-aziridinylmethylammonium salt (6), but not for 1-methoxymethylaziridine (7) and 1-aziridinemethanol. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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