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α -Aminonitriles: From Sustainable Preparation to Applications in Natural Product Synthesis.

Caroline GrundkeNina VierengelJason Sirleaf
Published in: Chemical record (New York, N.Y.) (2020)
Due to their numerous reactivity modes, α-aminonitriles represent versatile and valuable building blocks in organic total synthesis. Since their discovery by Adolph Strecker in 1850, this compound class has seen a wide dissemination in synthetic applications from laboratory to million-ton industrial scale and was extensively used in the syntheses of various classes of natural products. As these compounds provide a multitude of reactivity options, we feel that a broad overview of their multiple reaction modes may reveal less familiar opportunities for successful total synthesis planning. This personal account article will thus focus on α-aminonitriles used as key intermediates in selected natural product synthesis sequences which have been reported in the two decades since Enders' and Shilvock's seminal review. Natural α-aminonitriles will also briefly be treated.
Keyphrases
  • small molecule
  • multidrug resistant
  • heavy metals
  • wastewater treatment
  • genome wide
  • single cell
  • dna methylation
  • high resolution
  • risk assessment
  • liquid chromatography
  • solid phase extraction