Abstract
We report on a protocol for the hydroxyalkenylation of alkenes using an acridinium photoredox catalyst in combination with 1,2-bis(phenylsulfonyl)ethylene and water. Using the protocol, alkenes could be converted into the corresponding 1-phenylsulfonyl-4-hydroxyalkenes in good yields. The hydroxyalkenylation involves the nucleophilic hydroxylation of alkene-derived radical cations to give β-hydroxyalkyl radicals, which then undergo a radical addition/β-elimination sequence. The catalytic cycle is likely sustained by electron transfer from the acridine radical to the benzenesulfonyl radical, which is formed via a radical addition/elimination sequence.
Original language | English |
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Article number | e202400017 |
Journal | Helvetica Chimica Acta |
Volume | 107 |
Issue number | 5 |
DOIs | |
State | Published - May 2024 |
Keywords
- acridinium salt
- alkene-hydroxyalkenylation
- electron transfer
- photocatalysis