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张力脱氢-[2,2]对环芳烷实现平面手性构建及[2.2]对环芳烷官能团化

Strained Dehydro-[2,2]-paracyclophane Enabled Planar Chirality Construction and [2.2]Paracyclophane Functionalization.

作者信息

Zhang Xue, Zhou Yi, Yu Zhi-Xiang, Tung Chen-Ho, Xu Zhenghu

机构信息

School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.

College of Chemistry, Peking University, Beijing, 100871, China.

出版信息

Angew Chem Int Ed Engl. 2025 Feb 24;64(9):e202420667. doi: 10.1002/anie.202420667. Epub 2025 Feb 5.

Abstract

Planar chirality found tremendous use in many fields, such as chemistry, optics, and materials science. In particular, planar chiral [2.2]paracyclophanes (PCPs) are a type of structurally interesting and practically useful chiral compounds bearing unique electronic and photophysical properties and thus have been widely used in π-stacking polymers, organic luminescent materials, and as a valuable toolbox for developing chiral ligands or organocatalysts. However, the synthesis of chiral PCP derivatives remains a longstanding challenge. Current synthetic methods primarily rely on chiral preparative liquid chromatography separation or chemical and kinetic resolution reactions. Here, we report an enantioconvergent alkynylation of an in situ-formed dehydro-[2,2]-paracyclophane intermediate by asymmetric copper(I) catalysis. This approach enables the efficient synthesis of valuable planar chiral PCP building blocks and heterocycles with good yields and excellent enantioselectivity. The success of this reaction lies in the development of a practical route to access strained dehydro-[2,2]-paracyclophane intermediates, which can also be utilized in various strain-release nucleophilic or cycloaddition reactions to synthesize diverse functionalized PCPs. DFT calculations of this reaction suggest that the enantioselectivity is determined by the aryne complexation with chiral copper(I) acetylide and the subsequent insertion reaction.

摘要

平面手性在许多领域有广泛应用,如化学、光学和材料科学。特别是,平面手性[2.2]对环芳烷(PCP)是一类结构有趣且实用的手性化合物,具有独特的电子和光物理性质,因此已广泛应用于π-堆积聚合物、有机发光材料,并作为开发手性配体或有机催化剂的宝贵工具箱。然而,手性PCP衍生物的合成仍然是一个长期存在的挑战。目前的合成方法主要依赖于手性制备液相色谱分离或化学及动力学拆分反应。在此,我们报道了通过不对称铜(I)催化原位形成的脱氢-[2,2]-对环芳烷中间体的对映收敛炔基化反应。该方法能够高效合成有价值的平面手性PCP结构单元和杂环化合物,产率良好且对映选择性优异。该反应的成功在于开发了一条实用的路线来获得张力脱氢-[2,2]-对环芳烷中间体,该中间体也可用于各种应变释放亲核或环加成反应以合成各种功能化的PCP。该反应的密度泛函理论计算表明,对映选择性由芳炔与手性铜(I)乙炔化物的络合以及随后的插入反应决定。

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