Visible-light unmasking of heterocyclic quinone methide radicals from alkoxyamines

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Abstract

In nature, the unmasking of heterocyclic quinones to form stabilized quinone methide radicals is achieved using reductases (bioreduction). Herein, an alternative controllable room-temperature, visible-light activated protocol using alkoxyamines and bis-alkoxyamines is provided. Selective synthetic modification of the bis-alkoxyamine, allowed chromophore deactivation to give one labile alkoxyamine moiety.

Original languageEnglish (Ireland)
Pages (from-to)14665-14668
Number of pages4
JournalChemical Communications
Volume55
Issue number97
Publication statusPublished - 1 Nov 2019

Authors (Note for portal: view the doc link for the full list of authors)

  • Authors
  • Patrick Kielty, Pau Farras, Patrick McArdle, Dennis A Smith, Fawaz Aldabbagh

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