at Google ScholarTitle data
Bera, Sourav Sekhar ; Bahukhandi, Srishti Ballabh ; Empel, Claire ; Koenigs, Rene M.:
Catalyst-controlled site-selective N–H and C3-arylation of carbazole via carbene transfer reactions.
In: Chemical Communications.
Vol. 57
(2021)
.
- pp. 6193-6196.
ISSN 1364-548X
DOI: https://doi.org/10.1039/D1CC01863A
Abstract in another language
A site-selective direct arylation reaction of carbazole and other N-heterocycles with diazo-naphthalen-2(1H)-ones has been developed. While Au(I)-NHC catalysts lead to selective C3-arylation, palladium acetate allows for selective N–H arylation, displaying complete site-selectivity each. To show the applicability of these arylation reactions, one-pot, two-fold diarylation reactions of carbazole were demonstrated.
Further data
| Item Type: | Article in a journal |
|---|---|
| Refereed: | Yes |
| Institutions of the University: | Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry Faculties Faculties > Faculty of Biology, Chemistry and Earth Sciences Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Organic Chemistry II - Bioorganic Chemistry > Chair Organic Chemistry II - Bioorganic Chemistry - Univ.-Prof. Dr. René M. Koenigs Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Organic Chemistry II - Bioorganic Chemistry |
| Result of work at the UBT: | No |
| DDC Subjects: | 500 Science > 540 Chemistry |
| Date Deposited: | 01 Apr 2025 11:41 |
| Last Modified: | 07 Oct 2025 10:57 |
| URI: | https://eref.uni-bayreuth.de/id/eprint/93115 |