Silver-Catalyzed Site-Selective Ring-Opening and C-C Bond Functionalization of Cyclic Amines: Access to Distal Aminoalkyl-Substituted Quinones

Org Lett. 2019 Jun 21;21(12):4590-4594. doi: 10.1021/acs.orglett.9b01496. Epub 2019 Jun 11.

Abstract

Distal aminoalkyl-substituted quinones have been efficiently prepared through silver-catalyzed site-selective deconstruction and C-C bond transformation of unstrained N-acylated cyclic amines. This method enjoys mild reaction conditions, high selectivity, a broad scope of substrates, and a low catalytic loading of silver. This strategy can also be applied to the modification of peptides bearing cyclic amine residues.

Publication types

  • Research Support, Non-U.S. Gov't