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 language | English (Ireland) |
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Pages (from-to) | 14665-14668 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 55 |
Issue number | 97 |
Publication status | Published - 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