Highly selective and practical hydrogenation of functionalized (hetero)arenes
Arenes, and particularly heteroarenes are integral structural components of a variety of chemicals and represent a privileged class of bioactive compounds found in pharmaceuticals, agrochemicals and vitamins. Diastereoselective hydrogenation of multi-substituted (hetero)arenes offers an efficient and industrially relevant approach to convert these compounds into valuable, diversified 3D building blocks for applications for example in drug innovation. We show that a rationally designed Pt catalyst permits the general diastereoselective hydrogenation of a broad range of multi-substituted and functionalized arenes and heteroarenes using mild conditions. The corresponding cyclic products are obtained with very high diastereoselectivity (d.r. value up to 99/1). The practical applicability of this catalysis is illustrated by the straightforward preparation of a novel plasticizer on kg-scale under solvent-free conditions.
Authors
- Soumyashree Jena (ORCID: https://orcid.org/0000-0003-3296-9943)
- Kathrin Junge (ORCID: https://orcid.org/0000-0001-7044-8888)
- Haijun Jiao
- Robert Franke (ORCID: https://orcid.org/0000-0001-6077-820X)
- Hui Yang (ORCID: https://orcid.org/0000-0002-3536-0132)
- Lifeng Xiao
- Professor Dr. M. Beller
- Ruiyang Qu
- Hanan Atia
- Graham J. Hutchings
- Rongsheng Cai
- Stephan Bartling
- Ralf Jackstell
Institutions
- Chinese Academy of Sciences (CN)
- Evonik (Germany) (DE)
- Lanzhou Institute of Chemical Physics (CN)
- Leibniz Institute for Catalysis (DE)
- National Institute of Clean and Low-Carbon Energy (CN)
- Berliner Energieagentur (Germany) (DE)
- University of Wales Institute Cardiff (SG)
- Cardiff University (GB)
- Cardiff Metropolitan University (GB)
- Ruhr University Bochum (DE)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-02-25
- DOI
- https://doi.org/10.1038/s41467-026-68537-7
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Alexander von Humboldt-Stiftung
- China Scholarship Council
- Leibniz-Gemeinschaft