Photocatalytic [2 + 2] Cycloaddition in DNA-Encoded Chemistry

Org Lett. 2020 Apr 17;22(8):2908-2913. doi: 10.1021/acs.orglett.0c00574. Epub 2020 Apr 2.

Abstract

The on-DNA synthesis of highly substituted cyclobutanes was achieved through a photocatalytic [2 + 2] cycloaddition reaction in aqueous solution. Readily available DNA-tagged styrene derivatives were reacted with structurally diverse cinnamates in the presence of an iridium-based photocatalyst, Ir(ppy)2(dtbbpy)PF6, to forge two new C(sp3)-C(sp3) bonds. This transformation was demonstrated to have excellent functional group tolerance and allowed for the facile installation of a variety of heteroaromatic substituents on a densely functionalized cyclobutane scaffold.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cycloaddition Reaction
  • Cyclobutanes / chemistry*
  • DNA / chemical synthesis*
  • DNA / chemistry
  • Molecular Structure
  • Photochemical Processes

Substances

  • Cyclobutanes
  • DNA