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氟离子催化下无金属温和条件下通过分子内亲核芳香取代反应合成梯型共轭苯并双苯并呋喃

Fluoride-Ion-Catalyzed Synthesis of Ladder-type Conjugated Benzobisbenzofurans via Intramolecular Nucleophilic Aromatic Substitution Reaction under Metal-free and Mild Conditions.

作者信息

Sekino Katsutoshi, Shida Naoki, Shiki Ryosuke, Takigawa Natsuki, Nishiyama Hiroki, Tomita Ikuyoshi, Inagi Shinsuke

机构信息

Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8502, Japan.

PRESTO, Japan Science and Technology Agency (JST), 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

出版信息

Org Lett. 2020 Apr 17;22(8):2892-2896. doi: 10.1021/acs.orglett.0c00531. Epub 2020 Feb 25.

Abstract

The fluoride-ion-catalyzed synthesis of benzobisbenzofuran derivatives is described. Fluorine-containing aryl silyl ethers were reacted with 5 mol % of BuNF to give desired compounds in high yield under mild conditions. Syn-selective cyclization reaction was discovered for a particular compound as a kinetic product. Computational analysis revealed that the fluorine substituents in the anti-type benzobisbenzofurans affect the order of the molecular orbitals.

摘要

描述了氟离子催化的苯并双苯并呋喃衍生物的合成。含氟芳基硅醚与5 mol%的BuNF反应,在温和条件下以高产率得到所需化合物。发现一种特定化合物会发生顺式选择性环化反应生成动力学产物。计算分析表明,反式苯并双苯并呋喃中的氟取代基会影响分子轨道的顺序。

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