Nickel-catalyzed regiodivergent hydrosilylation of α-(fluoroalkyl)styrenes without defluorination
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41467-024-50743-w.pdf
Reference70 articles.
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2. Purser, S., Moore, P. R., Swallow, S. & Gouverneur, V. Fluorine in medicinal chemistry. Chem. Soc. Rev. 37, 320–330 (2008).
3. Kirsch, P. Modern Fluoroorganic Chemistry: Synthesis Reactivity, Applications. 2nd edn (Wiley-VCH, 2013).
4. Wang, J. et al. Fluorine in pharmaceutical industry: fluorine-containing drugs introduced to the market in the last decade (2001−2011). Chem. Rev. 114, 2432–2506 (2014).
5. Meanwell, N. A. Fluorine and fluorinated motifs in the design and application of biosisosteres for drug design. J. Med. Chem. 61, 5822–5880 (2018).
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis of Axially Chiral Monofluoroalkenes via Nickel-Catalyzed Reductive Cross-Coupling of gem-Difluoroalkenes;Organic Letters;2024-09-13
2. Regiodivergent Nickel-Catalyzed Hydrosilylation of α-(Fluoroalkyl)styrenes;Synfacts;2024-09-13
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