ArticleChemical science2019
Transition metal-free catalytic reduction of primary amides using an abnormal NHC based potassium complex: integrating nucleophilicity with Lewis acidic activation.
Article in Chemical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Article
- Tailoring tin-based perovskite crystallization via large cations and pseudo-halide anions for high mobility and high stable transistors.Science advances · 2025Article
- s-Block Metal Catalysts for the Hydroboration of Unsaturated Bonds.Chemical reviews · 2022Review
- Manganese-Catalyzed Hydroborations with Broad Scope.Angewandte Chemie (International ed. in English) · 2021Article
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Authors and funding
6 authors.
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Abstract
An abnormal N-heterocyclic carbene (aNHC) based potassium complex was used as a transition metal-free catalyst for reduction of primary amides to corresponding primary amines under ambient conditions. Only 2 mol% loading of the catalyst exhibits a broad substrate scope including aromatic, aliphatic and heterocyclic primary amides with excellent functional group tolerance. This method was applicable for reduction of chiral amides and utilized for the synthesis of pharmaceutically valuable precursors on a gram scale. During mechanistic investigation, several intermediates were isolated and characterized through spectroscopic techniques and one of the catalytic intermediates was characterized through single-crystal XRD. A well-defined catalyst and isolable intermediate along with several stoichiometric experiments,
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