Photoredox chemistry in the synthesis of 2-aminoazoles implicated in prebiotic nucleic acid synthesis

Chem Commun (Camb). 2020 Nov 14;56(88):13563-13566. doi: 10.1039/d0cc05752e. Epub 2020 Oct 14.

Abstract

Prebiotically plausible ferrocyanide-ferricyanide photoredox cycling oxidatively converts thiourea to cyanamide, whilst HCN is reductively homologated to intermediates which either react directly with the cyanamide giving 2-aminoazoles, or have the potential to do so upon loss of HCN from the system. Thiourea itself is produced by heating ammonium thiocyanate, a product of the reaction of HCN and hydrogen sulfide under UV irradiation.

MeSH terms

  • Azoles / chemical synthesis*
  • Azoles / chemistry
  • Molecular Structure
  • Nucleic Acids / chemical synthesis*
  • Nucleic Acids / chemistry
  • Oxidation-Reduction
  • Photochemical Processes
  • Prebiotics

Substances

  • Azoles
  • Nucleic Acids
  • Prebiotics