Abstract
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tricyclic aziridines. These undergo a range of novel palladium-catalyzed ring-opening and cycloaddition reactions, likely driven by their inherent strain, allowing incorporation of further functionality by fusing additional heterocyclic rings onto these already complex polycyclic cores. This rapid, 2-step access to complex sp3 – rich heterocycles should be of interest to those in the fields of drug discovery and natural product synthesis.
Original language | English |
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Pages (from-to) | 2302-2307 |
Journal | Chemical Science |
Volume | 7 |
Issue number | 3 |
Early online date | 4 Jan 2016 |
DOIs | |
Publication status | Published - 1 Mar 2016 |