1989 年 1989 巻 9 号 p. 1648-1651
Ring-opening reaction of optically active 2-ethylaziridine in water was found to give 1-(2-ethy1-1-aziridiny1)-2-butanaminek N-(2-aminobuty1)-1-(2-ethyl-1-aziridinyl-2-butanamine, and oligomers of 2-ethylaziridine. The structures of the products were elucidated on the basis of their infrared spectra and mass spectra. In this ring-opening reaction, the original configuration in the starting aziridine was retained in these products, suggesting the occurrence of N-CH12 bond cleavage in 2-ethylaziridine.
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