Kikushima Kotaro, Miyamoto Naoki, Watanabe Kazuma, Koseki Daichi, Kita Yasuyuki, Dohi Toshifumi
College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1, Nojihigashi, Kusatsu Shiga 525-8577, Japan.
Research Organization of Science and Technology, Ritsumeikan University, 1-1-1, Nojihigashi, Kusatsu Shiga 525-8577, Japan.
Org Lett. 2022 Mar 18;24(10):1924-1928. doi: 10.1021/acs.orglett.2c00294. Epub 2022 Mar 7.
High reactivity of trimethoxyphenyl (TMP)-iodonium(III) acetate for phenol -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 -arylation, verifying the applicability of this ligand- and counterion-assisted strategy.
实现了三甲氧基苯基(TMP)-碘鎓(III)乙酸盐对苯酚芳基化的高反应活性。首先确定TMP配体和乙酸根阴离子协同增强了对苯酚氧原子的亲电反应活性。所提出的方法能够以比先前报道的技术显著更高的产率获得各种二芳基醚。在芳基化过程中,包括脂肪醇、硼酸酯和空间位阻基团在内的各种官能团都能耐受,这验证了这种配体和抗衡离子辅助策略的适用性。