Synthesis of Structurally Diverse Polycyclic Arenes Using Tandem Oxidative Ring Expansion Strategy

IF 0.2 4区 化学 Q4 CHEMISTRY, ORGANIC Journal of Synthetic Organic Chemistry Japan Pub Date : 2023-11-01 DOI:10.5059/yukigoseikyokaishi.81.1062
Tienan Jin, Masahiro Terada
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Abstract

The impressive structural diversity of polycyclic arenes (PCAs) comprised of pentagon, hexagon, heptagon, and octagon rings has continued to drum up interest in the fields of synthetic chemistry and materials science owing to their tunable electronic properties in relation to their unique planar, twisted, and curved π-surface conformations. Although an array of synthetic strategies have been developed to construct both known and new PCA scaffolds in the past decades, flexible and expedient strategies for creating PCAs with differently sized rings embedded are rare. We describe herein our recent studies on the tandem oxidative ring expansion (TORE) strategy for the construction of structurally diverse PCAs involving intra- and intermolecular TORE reactions for hexagon-embedded PCAs, and intramolecular TORE reactions for O- or S-incorporated heptagon-embedded PCAs and octagon-embedded PCAs.
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用串联氧化扩环策略合成结构多样的多环芳烃
由五边形、六边形、七边形和八边形环组成的多环芳烃(PCAs)具有令人印象深刻的结构多样性,由于其独特的平面、扭曲和弯曲π面构象具有可调的电子性质,因此在合成化学和材料科学领域不断引起人们的兴趣。虽然在过去的几十年里,已经开发了一系列的合成策略来构建已知的和新的PCA支架,但用于制造嵌入不同大小环的PCA的灵活和方便的策略很少。本文描述了我们最近在构建结构多样的聚丙烯酸酯方面的串联氧化环扩张(TORE)策略的研究,包括六边形嵌入聚丙烯酸酯的分子内和分子间的TORE反应,以及O或s结合的七面嵌入聚丙烯酸酯和八边形嵌入聚丙烯酸酯的分子内TORE反应。
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来源期刊
CiteScore
0.30
自引率
0.00%
发文量
120
审稿时长
6-12 weeks
期刊介绍: Information not localized
期刊最新文献
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