Issue 2, 2024

Chemo- and enantioselective intramolecular silver-catalyzed aziridinations of carbamimidates

Abstract

Transition metal-catalyzed asymmetric nitrene transfer is a powerful method to generate enantioenriched amines found in natural products and bioactive molecules. A highly chemo- and enantioselective intramolecular silver-catalysed aziridination of 2,2,2-trichloroethoxysulfonyl (Tces)-protected carbamimidates gives [4.1.0]-bicyclic aziridines in good yields and up to 99% ee.

Graphical abstract: Chemo- and enantioselective intramolecular silver-catalyzed aziridinations of carbamimidates

Supplementary files

Article information

Article type
Communication
Submitted
21 Nov 2023
Accepted
29 Nov 2023
First published
30 Nov 2023

Chem. Commun., 2024,60, 224-227

Author version available

Chemo- and enantioselective intramolecular silver-catalyzed aziridinations of carbamimidates

T. A. Trinh, Y. Fu, D. B. Hu, S. A. Zappia, I. A. Guzei, P. Liu and J. M. Schomaker, Chem. Commun., 2024, 60, 224 DOI: 10.1039/D3CC05670H

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