ChemistryOpen (Jun 2019)

A Cyanide‐Free Synthesis of Acylcyanides through Ru‐Catalyzed C(sp3)‐H‐Oxidation of Benzylic Nitriles

  • M. Sc. Pascal Eisele,
  • M. Sc. Michael Bauder,
  • Dr. Shih‐Fan Hsu,
  • Prof. Dr. Bernd Plietker

DOI
https://doi.org/10.1002/open.201900130
Journal volume & issue
Vol. 8, no. 6
pp. 689 – 691

Abstract

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Abstract A practical method for generation of acylcyanides devoid of any external cyanide sources is presented that relies on a mild Ru‐catalyzed selective C−H‐oxidation of benzylic nitriles. The starting materials are smoothly generated through condensation of the corresponding carboxylic acid amides using silanes. The obtained acylcyanides can be employed in a plethora of transformation as exemplified to some larger extend in the sequence of C−H‐oxidation‐Tischenko‐rearrangement for the generation of structurally diverse benzoyloxycyanohydrines.

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