Peng Xiaopeng, Rahim Abdur, Peng Weijie, Jiang Feng, Gu Zhenhua, Wen Shijun
College of Pharmacy, Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Ministry of Education, Jiangxi Province Key Laboratory of Biomaterials and Biofabrication for Tissue Engineering, Gannan Medical University, Ganzhou341000, P.R. China.
State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, 651 Dongfeng East Road, Guangzhou510060, P. R. China.
Chem Rev. 2023 Jan 17;123(4):1364-416. doi: 10.1021/acs.chemrev.2c00591.
Hypervalent aryliodoumiums are intensively investigated as arylating agents. They are excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows the corresponding arylation reactions to be performed under mild conditions. In the past decades, acyclic aryliodoniums are widely explored as arylation agents. However, the unmet need for acyclic aryliodoniums is the improvement of their notoriously low reaction economy because the coproduced aryl iodides during the arylation are often wasted. Cyclic aryliodoniums have their intrinsic advantage in terms of reaction economy, and they have started to receive considerable attention due to their valuable synthetic applications to initiate cascade reactions, which can enable the construction of complex structures, including polycycles with potential pharmaceutical and functional properties. Here, we are summarizing the recent advances made in the research field of cyclic aryliodoniums, including the nascent design of aryliodonium species and their synthetic applications. First, the general preparation of typical diphenyl iodoniums is described, followed by the construction of heterocyclic iodoniums and monoaryl iodoniums. Then, the initiated arylations coupled with subsequent domino reactions are summarized to construct polycycles. Meanwhile, the advances in cyclic aryliodoniums for building biaryls including axial atropisomers are discussed in a systematic manner. Finally, a very recent advance of cyclic aryliodoniums employed as halogen-bonding organocatalysts is described.
高价芳基碘鎓盐作为芳基化试剂受到了广泛研究。它们是芳基卤化物的优良替代物,而且具有更好的反应活性,这使得相应的芳基化反应能够在温和条件下进行。在过去几十年里,无环芳基碘鎓盐作为芳基化试剂得到了广泛探索。然而,无环芳基碘鎓盐尚未满足的需求是提高其 notoriously 低的反应经济性,因为芳基化过程中副产的芳基碘化物常常被浪费。环状芳基碘鎓盐在反应经济性方面具有其固有优势,并且由于它们在引发级联反应方面的宝贵合成应用,开始受到相当多的关注,这能够构建复杂结构,包括具有潜在药物和功能特性的多环化合物。在此,我们总结了环状芳基碘鎓盐研究领域的最新进展,包括芳基碘鎓盐物种的新设计及其合成应用。首先,描述了典型二苯基碘鎓盐的一般制备方法,随后是杂环碘鎓盐和单芳基碘鎓盐的构建。然后,总结了引发的芳基化反应以及随后的多米诺反应以构建多环化合物。同时,系统地讨论了环状芳基碘鎓盐在构建包括轴手性异构体在内的联芳基方面的进展。最后,描述了环状芳基碘鎓盐作为卤素键有机催化剂的最新进展。