Copper-catalyzed <i>N</i> -arylation of isatins employing aryl(TMP)-iodonium salts
This work presents a general one-pot methodology for <i>N</i>-arylation of isatin functionalities employing aryl(2,4,6-trimethoxyphenyl)iodonium salts. The developed Cu-catalysed protocol works under mild conditions and is operationally straightforward. This synthetic approach demonstrates broad substrate scope, tolerating a wide range of electronically and sterically diverse aryl groups, thereby enabling access to a variety of <i>N</i>-arylated isatin products. Furthermore, two examples of post-synthetic modification highlight the utilization of the synthetic scaffolds.
Authors
- Raktim Abha Saikia (ORCID: https://orcid.org/0000-0003-4719-356X)
- Snata Deka (ORCID: https://orcid.org/0009-0008-2581-1519)
- Ashim Jyoti Thakur (ORCID: https://orcid.org/0000-0003-0923-6725)
- A. K. Rakshit
Institutions
- Tezpur University (IN)
- National Institute for Research and Development of Isotopic and Molecular Technologies (RO)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1039/d5ob01451d
- Citations
- 2
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.87