铜催化的对映体选择性脱氢-Diels-Alder 反应:轴向手性咔唑的原子经济合成

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2024-09-13 DOI:10.1002/anie.202411709
Hua-Hong Chen, Yang-Bo Chen, Jun-Zhe Gao, Long-Wu Ye, Bo Zhou
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引用次数: 0

摘要

脱氢-Diels-Alder(DDA)反应是一种构建芳香化合物的有效方法。然而,可能由于竞争性热反应的原因,对映体选择性 DDA 反应很少得到开发。在此,我们报告了一种通过乙烯基阳离子途径的铜催化对映体选择性 DDA 反应。该反应能以原子经济的方式合成轴向手性苯基和吲哚基咔唑,产量普遍极高,且具有良好至极佳的对映选择性。该方法是第一个非贵金属催化的对映选择性 DDA 反应实例。值得注意的是,由所构建的轴向手性咔唑衍生出的新手性配体和有机催化剂被证明可用于不对称催化。
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Copper-Catalyzed Enantioselective Dehydro-Diels–Alder Reaction: Atom-Economical Synthesis of Axially Chiral Carbazoles
The dehydro-Diels–Alder (DDA) reaction is a powerful method for the construction of aromatic compounds. However, the enantioselective DDA reaction has been rarely developed, probably due to the competitive thermal reaction. Herein, we report a copper-catalyzed enantioselective DDA reaction through vinyl cation pathway. The reaction leads to the atom-economical synthesis of axially chiral phenyl and indolyl carbazoles in generally excellent yields with good to excellent atroposelectivities. This methodology represents the first example of non-noble metal-catalyzed enantioselective DDA reaction. Notably, new chiral ligand and organocatalyst derived from the constructed axially chiral carbazole are demonstrated to be useful in asymmetric catalysis.
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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