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Ohashi M, Ueda Y, Ogoshi S. Nickel(0)-Mediated Transformation of Tetrafluoroethylene and Vinylarenes into Fluorinated Cyclobutyl Compounds. Angew Chem Int Ed Engl. 2017;56(9):2435-2439doi: 10.1002/anie.201610047.
Ohashi, M., Ueda, Y., & Ogoshi, S. (2017). Nickel(0)-Mediated Transformation of Tetrafluoroethylene and Vinylarenes into Fluorinated Cyclobutyl Compounds. Angewandte Chemie (International ed. in English), 56(9), 2435-2439. https://doi.org/10.1002/anie.201610047
Ohashi, Masato, et al. "Nickel(0)-Mediated Transformation of Tetrafluoroethylene and Vinylarenes into Fluorinated Cyclobutyl Compounds." Angewandte Chemie (International ed. in English) vol. 56,9 (2017): 2435-2439. doi: https://doi.org/10.1002/anie.201610047
Ohashi M, Ueda Y, Ogoshi S. Nickel(0)-Mediated Transformation of Tetrafluoroethylene and Vinylarenes into Fluorinated Cyclobutyl Compounds. Angew Chem Int Ed Engl. 2017 Feb 20;56(9):2435-2439. doi: 10.1002/anie.201610047. Epub 2017 Jan 23. PMID: 28111870.
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Angew Chem Int Ed Engl. 2017 Feb 20;56(9):2435-2439. doi: 10.1002/anie.201610047. Epub 2017 Jan 23.

Nickel(0)-Mediated Transformation of Tetrafluoroethylene and Vinylarenes into Fluorinated Cyclobutyl Compounds.

Angewandte Chemie (International ed. in English)

Masato Ohashi, Yuta Ueda, Sensuke Ogoshi

Affiliations

  1. Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka, 565-0871, Japan.

PMID: 28111870 DOI: 10.1002/anie.201610047

Abstract

In the presence of Ni

© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords: amines; fluorine; nickel; reaction mechanisms; synthetic methods

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