ReviewAngewandte Chemie (International ed. in English)2020
Synthetic Applications of Oxidative Aromatic Coupling-From Biphenols to Nanographenes.
Review in Angewandte Chemie (International ed. in English), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.
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Who cites it
69 citing papers in PubMed.
- Divergent Synthesis of Möbius and Hückel N-Heterocycloarenes From a Common Macrocyclic Backbone.Angewandte Chemie (International ed. in English) · 2026Article
- Amplified chiroptic response in a multi-helical penta-perylene structure.Chemical science · 2026Article
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- Straightforward synthesis of Solomon-red-BAPTA as NIR fluorescent sensorsRSC advances · 2026Article
- Room-Temperature Helix-to-Disc Conversion of Thia[6]helicene S,S-Dioxides to Coronene via In Situ Phenoxide Anion Generation.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026Article
- A CJournal of the American Chemical Society · 2026Article
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- Atroposelective Suzuki-Miyaura Coupling to Form 2-Amino-2'-Hydroxybiphenyls Enabled by sRuPhos.Angewandte Chemie (International ed. in English) · 2026Article
- Electrochemical imaging of thermochemical catalysis.Nature catalysis · 2026Article
- Bilayer nanographenes: structure, properties, and synthetic challenges.Chemical Society reviews · 2025Review
- Edge-condensation to access a crystalline planar icosagen cation with σ-aromaticity.Nature communications · 2025Article
- Benzo-Extended [JACS Au · 2025Article
- Dual Excitation and Dual Emission in a 1,4-Diazepine Bearing an Extended π-System.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Total Synthesis of (-)-Dimatairesinol via Regioselective Intermolecular Oxidative Phenol Coupling.Organic letters · 2025Article
- Ring Contraction of Cyclooctatetraenes toward Non-Benzenoid Polycyclic Aromatic Hydrocarbons by Au(111)-Catalysis and Bulk Pyrolysis.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Twofold 6π-Electrocyclization as a Route Toward Multi-Heteroatom-Doped Nanographenes Built on a 1,4-Dihydropyrrolo[3,2-b]pyrrole Core.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Enantiomerically Pure Helical Bilayer Nanographenes: A Straightforward Chemical Approach.Journal of the American Chemical Society · 2024Article
- Twenty Years of Graphene: From Pristine to Chemically Engineered Nano-Sized Flakes.Journal of the American Chemical Society · 2024Review
- Phenylsulfonate as a photolabile group for intramolecular carbon-carbon cross-coupling reactions.RSC advances · 2024Article
- Water-promoted oxidative coupling of aromatics with subnanometer palladium clusters confined in zeolites.Nature communications · 2024Article
9 more citing papers are in PubMed but not listed here.
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oxidative aromatic coupling occupies a fundamental place in the modern chemistry of aromatic compounds. It is a method of choice for the assembly of large and bewildering architectures. Considerable effort was also devoted to applications of the Scholl reaction for the synthesis of chiral biphenols and natural products. The ability to form biaryl linkages without any prefunctionalization provides an efficient pathway to many complex structures. Although the chemistry of this process is only now becoming fully understood, this reaction continues to both fascinate and challenge researchers. This is especially true for heterocoupling, that is, oxidative aromatic coupling with the chemoselective formation of a C-C bond between two different arenes. Analysis of the progress achieved in this field since 2013 reveals that many groups have contributed by pushing the boundary of structural possibilities, expanding into surface-assisted (cyclo)dehydrogenation, and developing new reagents.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.