Kim Nayoung, Choi Myungsoo, Suh Sung-Eun, Chenoweth David M
Ajou Energy Science Research Center, Ajou University, Suwon 16499, Republic of Korea.
Department of Chemistry, Ajou University, Suwon 16499, Republic of Korea.
Chem Rev. 2024 Oct 23;124(20):11435-11522. doi: 10.1021/acs.chemrev.4c00296. Epub 2024 Oct 9.
Arynes hold significance for the efficient fusion of (hetero) arenes with diverse substrates, advancing the construction of complex molecular frameworks. Employing multiple equivalents of arynes is particularly effective in the rapid formation of polycyclic cores found in optoelectronic materials and bioactive compounds. However, the inherent reactivity of arynes often leads to side reactions, yielding unanticipated products and underlining the importance of a detailed investigation into the use of multiple arynes to fine-tune their reactivity. This review centers on methodologies and syntheses in organic reactions involving multiple arynes, categorizing based on mechanisms like cycloadditions, σ-bond insertions, nucleophilic additions, and ene reactions, and discusses aryne polymerization. The categorization based on these mechanisms includes two primary approaches: the first entails multiple aryne engagement within a single step while the second approach involves using a single equivalent of aryne sequentially across multiple steps, with both requiring strict reactivity control to ensure precise aryne participation in each respective step. Additionally, the review provides an in-depth analysis of the selection of aryne precursors, organized chronologically and by activation strategy, offering a comprehensive background that supports the main theme of multiple aryne utilization. The expectation remains that this comprehensive review will be invaluable in designing advanced syntheses engaging multiple arynes.
芳炔对于(杂)芳烃与多种底物的高效融合具有重要意义,推动了复杂分子骨架的构建。使用多当量的芳炔在快速形成光电材料和生物活性化合物中发现的多环核心方面特别有效。然而,芳炔固有的反应性常常导致副反应,产生意想不到的产物,这突出了详细研究使用多个芳炔来微调其反应性的重要性。本综述聚焦于涉及多个芳炔的有机反应中的方法和合成,根据环加成、σ键插入、亲核加成和烯反应等机理进行分类,并讨论芳炔聚合反应。基于这些机理的分类包括两种主要方法:第一种是在一步反应中涉及多个芳炔的参与,而第二种方法是在多个步骤中依次使用单当量的芳炔,这两种方法都需要严格控制反应性,以确保芳炔在每个相应步骤中精确参与反应。此外,本综述按时间顺序并根据活化策略对芳炔前体的选择进行了深入分析,提供了一个支持多芳炔利用这一主题的全面背景。人们仍然期望,这一全面的综述在设计涉及多个芳炔的先进合成方法时将具有重要价值。