Nickel-Catalyzed Decyanative Reductive Coupling of Benzyl Nitriles with Aryl Chlorides toward the Synthesis of Diarylmethanes
Herein, nickel-catalyzed decyanative reductive cross-coupling of benzyl nitriles with aryl chlorides has been developed. The current protocol features a wide scope, good functional group compatibility, and excellent chemoselectivity, thus providing a powerful alternative to the known methods for the synthesis of diarylmethanes. Mechanistic studies demonstrate the formation of benzyl-nickel species as the key intermediate in the catalytic cycle.
Authors
- Yaqi Chen (ORCID: https://orcid.org/0000-0003-4822-3679)
- Xianmao Liu (ORCID: https://orcid.org/0000-0002-6510-9109)
- Yuanhong Ma (ORCID: https://orcid.org/0000-0001-6300-6897)
- Xueyu Liu
- Ni Qian
Institutions
- Hunan Normal University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-12-08
- DOI
- https://doi.org/10.1021/acs.orglett.5c04713
- Citations
- 1
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.94