Journal article
A Rhodium Nanoparticle-Lewis Acidic Ionic Liquid Catalyst for the Chemoselective Reduction of Heteroarenes.
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Karakulina A
Institut des sciences et ingénierie chimiques (ISIC), Ecole polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland).
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Gopakumar A
Institut des sciences et ingénierie chimiques (ISIC), Ecole polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland).
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Akçok İ
Institut des sciences et ingénierie chimiques (ISIC), Ecole polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland).
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Roulier BL
Institut des sciences et ingénierie chimiques (ISIC), Ecole polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland).
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LaGrange T
Interdisciplinary Centre for Electron Microscopy (CIME), Ecole polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland).
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Katsyuba SA
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Centre of the Russian Academy of Sciences, Arbuzov strasse 8, 420088 Kazan (Russia).
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Das S
Institut des sciences et ingénierie chimiques (ISIC), Ecole polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland). shoubhik.das@epfl.ch.
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Dyson PJ
Institut des sciences et ingénierie chimiques (ISIC), Ecole polytechnique fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland). paul.dyson@epfl.ch.
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Published in:
- Angewandte Chemie (International ed. in English). - 2016
English
We describe a catalytic system composed of rhodium nanoparticles immobilized in a Lewis acidic ionic liquid. The combined system catalyzes the hydrogenation of quinolines, pyridines, benzofurans, and furan to access the corresponding heterocycles, important molecules present in fine chemicals, agrochemicals, and pharmaceuticals. The catalyst is highly selective, acting only on the heteroaromatic ring, and not interfering with other reducible functional groups.
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Language
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Open access status
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closed
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Identifiers
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Persistent URL
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https://sonar.ch/global/documents/176920
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