New Approaches in Catalytic Reactions Using Triphos: A Classical Privileged Ligand

Over the past decades, multiple catalytic transformations have been feasible due to the application of triphos as ligand. Its particular fac coordination mode, to a transition metal center provides a suitable flexibility enabling variation on the coordination mode resulting in metal stabilization. Most of the reported catalytic reactions have been dominated by the use of the ruthenium‐triphos system, either by application of well‐defined complexes or the in situ formed complex. However, in the last years, the emergence of cobalt complexes with comparable or even superior catalytic performance than ruthenium have been reported. In this review, the use of triphos is focussed in selected reactions such as N ‐alkylation, formic acid dehydrogenation, and bond cleavage.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-06-28
DOI
https://doi.org/10.1002/ejoc.202500327
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

New Approaches in Catalytic Reactions Using Triphos: A Classical Privileged Ligand

Susan Lühr
European Journal of Organic Chemistry
Asymmetric Hydrogenation and Catalysis
article

New Approaches in Catalytic Reactions Using Triphos: A Classical Privileged Ligand

Susan Lühr
article en

Abstract

Over the past decades, multiple catalytic transformations have been feasible due to the application of triphos as ligand. Its particular fac coordination mode, to a transition metal center provides a suitable flexibility enabling variation on the coordination mode resulting in metal stabilization. Most of the reported catalytic reactions have been dominated by the use of the ruthenium‐triphos system, either by application of well‐defined complexes or the in situ formed complex. However, in the last years, the emergence of cobalt complexes with comparable or even superior catalytic performance than ruthenium have been reported. In this review, the use of triphos is focussed in selected reactions such as N ‐alkylation, formic acid dehydrogenation, and bond cleavage.

European Journal of Organic ChemistryVol. 28(41)
University of Chile (CL)
Deutscher Akademischer Austauschdienst, Eberhard Karls Universität Tübingen, Johannes Gutenberg-Universität Mainz, Universidad de Chile, Universität Rostock, Leibniz-Gemeinschaft
Openalex Percentile: Top 88%
Asymmetric Hydrogenation and Catalysis
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New Approaches in Catalytic Reactions Using Triphos: A Classical Privileged Ligand — Susan Lühr · European Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS