• Media type: E-Article
  • Title: Selective Phthalimido-N-oxyl (PINO)-Catalyzed C–H Cyanation of Adamantane Derivatives
  • Contributor: Berndt, Jan-Philipp; Erb, Frederik; Ochmann, Lukas; Beppler, Jaqueline; Schreiner, Peter
  • Published: Georg Thieme Verlag KG, 2019
  • Published in: Synlett, 30 (2019) 4, Seite 493-498
  • Language: English
  • DOI: 10.1055/s-0037-1610403
  • ISSN: 0936-5214; 1437-2096
  • Origination:
  • Footnote:
  • Description: We present a new method for the selective C(sp3)–H cyanation of adamantane derivatives with PINO as the hydrogen abstracting reagent. A cyano radical is thereby transferred from p -toluenesulfonyl cyanide, allowing the cyanation of adamantane derivatives in up to 71% yield. The protocol presents a novel way to orthogonally functionalized adamantanes that are otherwise difficult to prepare. Mechanistic studies support the hypothesis of a radical pathway.