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Updated: Feb 11, 2026

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Novel Asymmetric and Stereospecific Aziridination of Alkenes with a Chiral Nitridomanganese Complex
Satoshi Minakata1, Takeya Ando1, Masaaki Nishimura1
1Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871 (Japan), Fax: (+81) 6-6879-7402.
Abstract:
The addition of pyridine N-oxide is necessary to obtain high enantioselectivities in the asymmetric aziridination of styrene derivatives through transfer of a nitrogen atom from chiral, toluenesulfonic anhydride activated nitridomanganese complex 1 [Eq. (a)]. Remarkably, high stereospecificity was observed in all the aziridinations of trans- and cis-1,2-disubstituted alkenes. R1 =H, Me, nPr, iPr; R2 =H, Me; Ts=p-toluenesulfonyl.
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