Nickel-Catalyzed Decarboxylative Cross-Coupling of NHPI Esters to Access 1,4-Dialkylbenzenes
A practical nickel-catalyzed decarboxylative cross-coupling of <i>N</i>-hydroxyphthalimide esters with 1,4-diiodobenzene analogues has been developed. Under mild reaction conditions, a series of structurally interesting 1,4-dialkylbenzene analogues have been accessed with good functional group tolerance, which are versatile precursors for organic synthesis and a kind of important unit for bioactive molecules, polymers, and other materials. The synthetic application of this methodology was demonstrated by the synthesis of 3-6-dialkylcarbazole derivatives.
Authors
- Peng-Lin Zhang
- Yang Guo (ORCID: https://orcid.org/0000-0001-8975-9387)
- Lan Yang (ORCID: https://orcid.org/0000-0002-8683-2726)
- Siyu Gao (ORCID: https://orcid.org/0000-0003-4829-5605)
- Y.-H. Tang
Institutions
- Tianjin University of Science and Technology (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2024-12-03
- DOI
- https://doi.org/10.1021/acs.joc.4c02371
- Citations
- 4
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.00
Funders
- National Natural Science Foundation of China
- Tianjin University of Science and Technology