Alexander E. Teuten

ORCID: 0000-0002-9674-544X
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Research Areas
  • Catalytic C–H Functionalization Methods
  • Radical Photochemical Reactions
  • Sulfur-Based Synthesis Techniques

University of Southampton
2022

Electro-reductive radical cyclisation of aryl halides affords the corresponding hetero- and carbo-cycles in an undivided flow reactor equipped with steel carbon electrodes using organic mediator. A dissolving metal anode is not needed, mediator can be employed a sub-stoichiometric amount (0.05 equiv), increasing practical utility cathodic cyclisation. The methodology applied to O-, N-, C-tethers, yielding tricyclic fused spiro systems. In absence mediator, major pathway hydrogenolysis C-X bond, 2 e

10.1002/anie.202203694 article EN Angewandte Chemie International Edition 2022-07-05

Abstract Electro‐reductive radical cyclisation of aryl halides affords the corresponding hetero‐ and carbo‐cycles in an undivided flow reactor equipped with steel carbon electrodes using organic mediator. A dissolving metal anode is not needed, mediator can be employed a sub‐stoichiometric amount (0.05 equiv), increasing practical utility cathodic cyclisation. The methodology applied to O‐, N‐, C‐tethers, yielding tricyclic fused spiro systems. In absence mediator, major pathway...

10.1002/ange.202203694 article EN Angewandte Chemie 2022-07-05
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