Citation: Yubei Dai, Fang Wang, Shengqing Zhu, Lingling Chu. Selective Ni-catalyzed cross-electrophile coupling of alkynes, fluoroalkyl halides, and vinyl halides[J]. Chinese Chemical Letters, ;2022, 33(8): 4074-4078. doi: 10.1016/j.cclet.2021.12.050 shu

Selective Ni-catalyzed cross-electrophile coupling of alkynes, fluoroalkyl halides, and vinyl halides

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, China

lingling.chu1@dhu.edu.cn

Received Date: 27 October 2021
Revised Date: 21 December 2021
Accepted Date: 22 December 2021
Available Online: 26 December 2021

Figures(5)

We report a Ni-catalyzed three-component cross-electrophile coupling of alkynes with alkenyl halides and fluoroalkyl halides to generate fluoroalkyl-incorporated 1,3-dienes. This mild and operationally simple protocol is distinguished by its broad substrate scope and excellent chemo-, regio-, and stereo-selectivity, offering a new and organometallic agent-free platform for the construction of fluoroalkyl-incorporated diene motifs. Preliminary mechanistic studies have been conducted to probe the potential reaction pathway.
- Fluoroalkylation,
- Cross-electrophile coupling,
- Nickel catalysis,
- Difunctionalization,
- Alkynes
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