Journal of Organic Chemistry

Mechanism of the isomerization of 1-(arylthiocarbonyl) aziridines to 2-(arylthioalkyl) isocyanates

DA Tomalia, DP Sheetz, GE Ham

Index: Tomalia,D.A. et al. Journal of Organic Chemistry, 1970 , vol. 35, # 1 p. 47 - 52

Full Text: HTML

Citation Number: 5

Abstract

It has been shown that the isomerization of 1-(arylthiocarbony1) aziridines to 2-(arylthioalkyl) isocyanates is catalyzed by triethylamine or thiophenolate ion and may occur under relatively mild conditions (25-77'). 1-(Arylthiocarbonyl)-2-methylaziridines rearranged to their isomeric isocyanates by selective ring fission at the unsubstituted aziridine ring carbon, thus indicating the SN2 character of these rearrangements. Kinetic experiments have shown ...

Related Articles:

More Articles...