Enantioselective Ni-catalyzed reductive cross-coupling of propargyl halides with vinyl halides to skipped enynes
<h2>Abstract</h2> Skipped enynes represent valuable structural motifs in synthetic chemistry due to their unique reactivity and prevalence in complex molecules. Herein, we describe a streamlined approach for the enantioselective synthesis of chiral skipped enynes via nickel-catalyzed asymmetric reductive cross-coupling between propargyl halides and vinyl halides. This transformation offers several notable advantages, including the use of readily available starting materials, mild reaction conditions, broad functional group tolerance, and potential for diverse downstream functionalizations.
Authors
- Hang Zhou (ORCID: https://orcid.org/0000-0002-6525-3514)
- Zhong‐Lin Tao (ORCID: https://orcid.org/0009-0008-4953-9177)
- Yingsheng Zhao (ORCID: https://orcid.org/0000-0002-6142-7839)
- Guangxia Wang (ORCID: https://orcid.org/0000-0002-5638-4838)
Institutions
- Hunan University (CN)
Publication Details
- Journal
- Tetrahedron Chem
- Published
- 2025-08-29
- DOI
- https://doi.org/10.1016/j.tchem.2025.100145
- Citations
- 1
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Natural Science Foundation of China
- Hunan University
- Natural Science Foundation of Hunan Province
- Fundamental Research Funds for the Central Universities