Department of Chemistry, Ben-Gurion University of the Negev , Beer-Sheva 84105, Israel.
J Am Chem Soc. 2017 Sep 27;139(38):13404-13413. doi: 10.1021/jacs.7b05898. Epub 2017 Sep 15.
A novel catalytic system for oxidative cross-coupling of readily oxidized phenols with poor nucleophilic phenolic partners based on an iron meso-tetraphenylporphyrin chloride (Fe[TPP]Cl) complex in 1,1,1,3,3,3-hexafluoropropan-2-ol (HFIP) was developed. The unique chemoselectivity of this reaction is attributed to the coupling between a liberated phenoxyl radical with an iron-ligated phenolic coupling partner. The conditions are scalable for preparing a long list of unsymmetrical biphenols assembled from a less reactive phenolic unit substituted with alkyl or halide groups.
开发了一种基于铁卟啉氯(Fe[TPP]Cl)配合物的新型催化体系,可在 1,1,1,3,3,3-六氟异丙醇(HFIP)中实现易氧化酚与亲核性差的酚类偶联物的氧化交叉偶联。该反应具有独特的化学选择性,这归因于游离的酚氧自由基与铁配位的酚偶联物之间的偶联。该条件可扩展用于制备由烷基或卤代基团取代的反应性较低的酚单元组装的一系列不对称联苯。