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Showing 1–2 of 2 results
Advanced filters: Author: Alexander P. Pulis Clear advanced filters
  • Benzothiophenes are common motifs in bioactive compounds, but selective functionalization at C3 is challenging. Here the authors report a method starting from benzothiophene S-oxides via an interrupted Pummerer reaction, giving access to a range of C3-alkylated and -arylated products.

    • Harry J. Shrives
    • José A. Fernández-Salas
    • David J. Procter
    ResearchOpen Access
    Nature Communications
    Volume: 8, P: 1-7
  • Amines are highly valued molecules, used to understand biological processes and in the discovery of new medicines. However, medium-sized cyclic and macrocyclic amines are extremely challenging to synthesize and are therefore underutilized. Now, up to 15-membered cyclic amines can be formed directly from smaller, more accessible rings via an organoborane-catalysed two-carbon-unit C–C bond insertion.

    • Maryia Barysevich
    • Alexander P. Pulis
    News & Views
    Nature Chemistry
    Volume: 17, P: 1299-1300