Issue 41, 2020

Rhodium(iii)-catalyzed synthesis of spirocyclic isoindole N-oxides and isobenzofuranones via C–H activation and spiroannulation

Abstract

Rhodium(III)-catalyzed mild and oxidative [4+1] spiroannulation has been realized via C–H activation of oximes and benzoic acids with 1-diazonaphthelen-2(1H)-ones as coupling reagents. This transformation integrates C–H activation and dearomatization and provides a direct approach to spirocyclic isoindole N-oxides and isobenzofuranones with functional group tolerance.

Graphical abstract: Rhodium(iii)-catalyzed synthesis of spirocyclic isoindole N-oxides and isobenzofuranones via C–H activation and spiroannulation

Supplementary files

Article information

Article type
Communication
Submitted
01 Feb 2020
Accepted
02 Apr 2020
First published
03 Apr 2020

Chem. Commun., 2020,56, 5528-5531

Rhodium(III)-catalyzed synthesis of spirocyclic isoindole N-oxides and isobenzofuranones via C–H activation and spiroannulation

X. Han, L. Kong, J. Feng and X. Li, Chem. Commun., 2020, 56, 5528 DOI: 10.1039/D0CC00830C

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