Atroposelective Ring Opening of Cyclic Diaryliodonium Salts with Bulky Anilines Controlled by a Chiral Cobalt(III) Anion

Abstract
The present work demonstrates a CuCl and anionic chiral cobalt(III)-catalyzed enantioselective ring-opening reaction. The small-size, ligand-free copper species enabled the cross-coupling of iodonium salts with a series of bulky aromatic amines in high ee values. The chiral cobalt(III) anion causes appreciable chemical shift changes of cyclic diaryliodoniums in(1)H NMR spectra.
Funding Information
  • Innovative Research Group Project of the National Natural Science Foundation of China (21871241)
  • Fundamental Research Funds for the Central Universities (WK2060190086)

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