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. Author manuscript; available in PMC: 2014 Sep 26.
Published in final edited form as: Science. 2014 Jan 3;343(6166):61–65. doi: 10.1126/science.1245727

Fig. 2.

Fig. 2

Direct and stereospecific N-H aziridination of olefins. Reactions were conducted at 0.1M using 2,2,2-trifluoroethanol as solvent and at 0.5 mmol scale unless otherwise indicated. To obtain crystalline material, 10s was O-acetylated and N-tosylated (Ts = para-toluenesulfonyl) to afford derivative 10ss.