Metal-free double azide addition to strained alkynes of an octadehydrodibenzo[12]annulene derivative with electron-withdrawing substituents

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC Beilstein Journal of Organic Chemistry Pub Date : 2024-09-04 DOI:10.3762/bjoc.20.191
Naoki Takeda, Shuichi Akasaka, Susumu Kawauchi, Tsuyoshi Michinobu
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Abstract

Strain-promoted azide–alkyne cycloaddition (SpAAC) is a powerful tool in the field of bioconjugation and materials research. We previously reported a regioselective double addition of organic azides to octadehydrodibenzo[12]annulene derivatives with electron-rich alkyloxy substituents. In order to increase the reaction rate, electron-withdrawing substituents were introduced into octadehydrodibenzo[12]annulene. In this report, the synthesis of new octadehydrodibenzo[12]annulene derivatives, regioselective double addition of organic azides, and an application to crosslinking polymers are described.

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Beilstein J. Org. Chem. 2024, 20, 2234–2241. doi:10.3762/bjoc.20.191

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八代氢二苯并[12]萘衍生物与具有电子撤回取代基的受约束炔的无金属双叠氮加成反应
摘要应变促进叠氮化物–炔环加成(SpAAC)是生物共轭和材料研究领域的一种有力工具。我们曾报道过有机叠氮化物与具有富电子烷氧基取代基的八代氢二苯并[12]蒽衍生物的区域选择性双加成反应。为了提高反应速率,我们在八代氢二苯并[12]萘中引入了抽电子取代基。本报告介绍了新的八代氢二苯并[12]萘衍生物的合成、有机叠氮化物的区域选择性双加成以及在交联聚合物中的应用。Chem.2024, 20, 2234–2241. doi:10.3762/bjoc.20.191
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来源期刊
CiteScore
4.90
自引率
3.70%
发文量
167
审稿时长
1.4 months
期刊介绍: The Beilstein Journal of Organic Chemistry is an international, peer-reviewed, Open Access journal. It provides a unique platform for rapid publication without any charges (free for author and reader) – Platinum Open Access. The content is freely accessible 365 days a year to any user worldwide. Articles are available online immediately upon publication and are publicly archived in all major repositories. In addition, it provides a platform for publishing thematic issues (theme-based collections of articles) on topical issues in organic chemistry. The journal publishes high quality research and reviews in all areas of organic chemistry, including organic synthesis, organic reactions, natural product chemistry, structural investigations, supramolecular chemistry and chemical biology.
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