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前所未有的碳-碳键形成:2,4-二硝基苯磺酸与活性亚甲基化合物的原位亲核取代反应

Unprecedented C-C Bond Formation Ipso Nucleophilic Substitution of 2,4-Dinitrobenzene Sulfonic Acid with Active Methylene Compounds.

作者信息

Mondal Sandip, Dolai Gobinda, Mandal Bhubaneswar

机构信息

Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati 781039, India.

出版信息

ACS Omega. 2022 Dec 21;8(1):1401-1409. doi: 10.1021/acsomega.2c06865. eCollection 2023 Jan 10.

Abstract

The sulfonic acid functionalization of sufficiently electron-deficient benzene sulfonic acids undergoes ipso nucleophilic substitution with various active methylene compounds, leading to new C-C bond formation. Good to excellent yields are obtained under mild conditions without transition-metal (Pd or Cu) catalyst, PTC, and ligand. No solid waste is generated. It is a highly effective strategy for incorporating various active methylene compounds into the nitro-substituted benzene ring. This method has been applied not only for synthesizing APIs but also in materials chemistry. It shows a novel route for creating heavily crowded all-carbon quaternary centers. Carbon-carbon bond formation by substituting a sulfonic acid group was unknown.

摘要

具有足够缺电子性的苯磺酸的磺酸官能化会与各种活性亚甲基化合物发生本位亲核取代反应,从而形成新的碳-碳键。在温和条件下,无需过渡金属(钯或铜)催化剂、相转移催化剂(PTC)和配体,即可获得良好至优异的产率。不会产生固体废弃物。这是一种将各种活性亚甲基化合物引入硝基取代苯环的高效策略。该方法不仅已应用于合成活性药物成分(APIs),还应用于材料化学领域。它展示了一条创建高度拥挤的全碳季中心的新途径。通过磺酸基团取代来形成碳-碳键此前并不为人所知。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/376f/9835781/5cfeca80dcd1/ao2c06865_0004.jpg

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