TDAE strategy for the synthesis of 2,3-diaryl N-tosylaziridines

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Abstract

We report herein an original and rapid synthesis of 2,3-diaryl N-tosylaziridines by TDAE strategy starting from ortho- or para- nitro(dichloromethyl)benzene derivatives and N-tosylimines. A mixture of cis/trans isomers was isolated from 1-(dichloromethyl)-4- nitrobenzene, whereas only trans-aziridines were obtained from ortho-nitro derivatives. © 2013 by the authors.

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Khoumeri, O., Spitz, C., Terme, T., & Vanelle, P. (2013). TDAE strategy for the synthesis of 2,3-diaryl N-tosylaziridines. Molecules, 18(7), 7364–7375. https://doi.org/10.3390/molecules18077364

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