Reactions of Aziridines with Metal Halides in Liquid Sulfur Dioxide

Abstracts of the Riga Technical University 55th International Scientific Conference: Section: Material Science and Applied Chemistry 2014
Jevgeņija Lugiņina, Māris Turks

In the past decades aziridines have played a role of versatile intermidiates and important precursors for the synthesis of nitrogen-containing active compounds. Modification of aziridine cycle leads formation of agents of different classes, such as heterocycles. Because of the rig strain, the most common transformations of aziridine cycle are the nucleophilic ring-opening reactions (NROR). Here we present a new synthetic process of aziridine opening with metal halides and other nucleophiles in liquid sulfur dioxide.

Keywords
sulfur dioxide, aziridine ring opening

Lugiņina, J., Turks, M. Reactions of Aziridines with Metal Halides in Liquid Sulfur Dioxide. In: Abstracts of the Riga Technical University 55th International Scientific Conference: Section: Material Science and Applied Chemistry, Latvia, Riga, 14-17 October, 2014. Riga: RTU Press, 2014, pp.21-21. ISBN 9789934105920.

Publication language
English (en)