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      Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese-PNN pincer complex.

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          Abstract

          Novel well-defined NNP and PNP manganese pincer complexes have been synthetized and fully characterized. The catalyst Mn-2 containing an imidazolyaminolphosphino ligand shows high activity and selectivity in the hydrogenation of a wide range of secondary and tertiary amides to the corresponding alcohols and amines, under relatively mild conditions. For the first time, more challenging substrates like primary aromatic amides including an actual herbicide can also be hydrogenated using this earth-abundant metal-based pincer catalyst.

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          Author and article information

          Journal
          Chem Sci
          Chemical science
          Royal Society of Chemistry (RSC)
          2041-6520
          2041-6520
          May 01 2017
          : 8
          : 5
          Affiliations
          [1 ] Leibniz-Institut für Katalyse , e.V. Albert-Einstein Str. 29a , 18059 Rostock , Germany . Email: matthias.beller@catalysis.de.
          [2 ] Instituto di Chimica Biomolecolare , Consiglio Nazionale delle Ricerche , Tr. La Crucca 3 , 07100 Sassari , Italy.
          Article
          c7sc00138j
          10.1039/c7sc00138j
          6092716
          30155202
          812d2c22-b316-4d66-abb9-ddadc55669e6
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