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Tarn C. Johnson

Researcher at University of Warwick

Publications -  7
Citations -  811

Tarn C. Johnson is an academic researcher from University of Warwick. The author has contributed to research in topics: Catalysis & Transfer hydrogenation. The author has an hindex of 4, co-authored 6 publications receiving 748 citations. Previous affiliations of Tarn C. Johnson include Coventry Health Care.

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Hydrogen generation from formic acid and alcohols using homogeneous catalysts

TL;DR: This tutorial review describes recent progress in the development of homogeneous catalytic methodology for the direct generation of hydrogen gas from formic acid and alcohols.
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Application of ruthenium complexes of triazole-containing tridentate ligands to asymmetric transfer hydrogenation of ketones.

TL;DR: The synthesis of a series of tridentate ligands based on a homochiral 1,2-diamine structure attached to a triazole group and their subsequent applications to the asymmetric transfer hydrogenation of ketones are described.
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(Cyclopentadienone)iron Shvo Complexes: Synthesis and Applications to Hydrogen Transfer Reactions

TL;DR: In this article, a series of (cyclopendienone)iron tricarbonyl complexes were prepared using an intramolecular cyclization strategy and applied to the catalysis of the oxidation of alcohols to aldehydes and ketones.
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Developing asymmetric iron and ruthenium-based cyclone complexes; complex factors influence the asymmetric induction in the transfer hydrogenation of ketones

TL;DR: The preparation of a range of asymmetric iron and ruthenium-cyclone complexes, and their application to the asymmetric reduction of a ketone, are described, representing the first example of asymmetrical ketone reduction using an iron cyclone catalyst.
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Three-Component Synthesis of Pyridylacetic Acid Derivatives by Arylation/Decarboxylative Substitution of Meldrum’s Acids

TL;DR: In this article , a three-component synthesis of substituted pyridylacetic acid derivatives is presented, based on the dual reactivity of Meldrum's acid derivatives, initially as nucleophiles to perform substitution on activated pyridine-Noxides, then as electrophiles with a range of nucleophilia to trigger ring-opening and decarboxylation.