Ligand- and Counterion-Assisted Phenol O‑Arylation with TMP-Iodonium(III) Acetates

High reactivity of trimethoxyphenyl (TMP)-iodonium­(III) acetate for phenol O-arylation was achieved. It was first determined that the TMP ligand and acetate anion cooperatively enhance the electrophilic reactivity toward phenol oxygen atoms. The proposed method provides access to various diaryl eth...

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Veröffentlicht in:Organic letters 2022-03, Vol.24 (10), p.1924-1928
Hauptverfasser: Kikushima, Kotaro, Miyamoto, Naoki, Watanabe, Kazuma, Koseki, Daichi, Kita, Yasuyuki, Dohi, Toshifumi
Format: Artikel
Sprache:eng
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Zusammenfassung:High reactivity of trimethoxyphenyl (TMP)-iodonium­(III) acetate for phenol O-arylation was achieved. It was first determined that the TMP ligand and acetate anion cooperatively enhance the electrophilic reactivity toward phenol oxygen atoms. The proposed method provides access to various diaryl ethers in significantly higher yields than the previously reported techniques. Various functional groups, including aliphatic alcohol, boronic ester, and sterically hindered groups, were tolerated during O-arylation, verifying the applicability of this ligand- and counterion-assisted strategy.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.2c00294