Synthesis of pyrrole-imidazole polyamide oligomers based on a copper-catalyzed cross-coupling strategy

Bioorg Med Chem Lett. 2017 May 15;27(10):2197-2200. doi: 10.1016/j.bmcl.2017.03.052. Epub 2017 Mar 29.

Abstract

Pyrrole-imidazole (Py-Im) polyamides are useful tools for chemical biology and medicinal chemistry studies due to their unique binding properties to the minor groove of DNA. We developed a novel method of synthesizing Py-Im polyamide oligomers based on a Cu-catalyzed cross-coupling strategy. All four patterns of dimer fragments could be synthesized using a Cu-catalyzed Ullmann-type cross-coupling with easily prepared monomer units. Moreover, we demonstrated that pyrrole dimer, trimer, and tetramer building blocks for Py-Im polyamide synthesis were accessible by combining site selective iodination of the pyrrole/pyrrole coupling adduct.

Keywords: Copper; Cross-coupling; Polyamides; Synthetic methods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Binding Sites
  • Catalysis
  • Copper / chemistry*
  • DNA / chemistry
  • DNA / metabolism
  • Imidazoles / chemistry*
  • Nylons / chemistry*
  • Pyrroles / chemistry*

Substances

  • Antineoplastic Agents
  • Imidazoles
  • Nylons
  • Pyrroles
  • Copper
  • DNA