Issue 14, 2021

Friedel–Crafts acylation of antiaromatic norcorroles: electronic and steric modulation of the paratropic current

Abstract

Acyl chlorides react with norcorrolatonickel(II) in dichloromethane in the presence of AlCl3 at room temperature affording two isomeric monoketone derivatives in moderate yields. For acetyl chloride, also diketones were detected and separated. Spectroscopic and electrochemical characterization studies were corroborated using DFT calculations.

Graphical abstract: Friedel–Crafts acylation of antiaromatic norcorroles: electronic and steric modulation of the paratropic current

Supplementary files

Article information

Article type
Research Article
Submitted
21 Apr 2021
Accepted
07 Jun 2021
First published
07 Jun 2021

Org. Chem. Front., 2021,8, 3639-3652

Friedel–Crafts acylation of antiaromatic norcorroles: electronic and steric modulation of the paratropic current

S. Li, O. Smaga, Y. Sun, X. Li, M. Pawlicki, M. Sukniewicz and P. J. Chmielewski, Org. Chem. Front., 2021, 8, 3639 DOI: 10.1039/D1QO00621E

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