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Planar Tetraindolodipleiadiene via Zirconium-Promoted Intramolecular Indolyl C4–H Homocoupling
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.198510461openalex-snapshot
Synthesis of Dipleiadiene by “Serendipity”
inferredcites →https://doi.org/10.1002/anie.201206699openalex-snapshot
A Boron‐Containing PAH as a Substructure of Boron‐Doped Graphene
inferredcites →https://doi.org/10.1002/anie.201707505openalex-snapshot
From Fenestrindane towards Saddle‐Shaped Nanographenes Bearing a Tetracoordinate Carbon Atom
inferredcites →https://doi.org/10.1002/anie.201711437openalex-snapshot
A Dipleiadiene‐Embedded Aromatic Saddle Consisting of 86 Carbon Atoms
inferredcites →https://doi.org/10.1002/anie.201904153openalex-snapshot
Stable Cross‐Conjugated Tetrathiophene Diradical
inferredcites →https://doi.org/10.1002/anie.201914416openalex-snapshot
Dicyclohepta[ijkl,uvwx]rubicene with Two Pentagons and Two Heptagons as a Stable and Planar Non‐benzenoid Nanographene
inferredcites →https://doi.org/10.1002/anie.202010077openalex-snapshot
Conformation and Aromaticity Switching in a Curved Non‐Alternant sp 2 Carbon Scaffold
inferredcites →https://doi.org/10.1002/anie.202017328openalex-snapshot
Indolo[3,2,1‐ jk ]carbazole Embedded Multiple‐Resonance Fluorophors for Narrowband Deep‐blue Electroluminescence with EQE≈34.7 % and CIE y ≈0.085
inferredcites →https://doi.org/10.1002/anie.202100260openalex-snapshot
Construction of Heptagon‐Containing Molecular Nanocarbons
inferredcites →https://doi.org/10.1002/anie.202110538openalex-snapshot
Azepine‐ or Azocine‐Embedded Hexabenzocoronene Derivatives as Nitrogen‐Doped Saddle or Saddle‐Helix Nanographenes
inferredcites →https://doi.org/10.1002/hlca.19960790613openalex-snapshot
The Radical Ions of Dipleiadiene (Dicyclohepta[de,ij]naphthalene) and Its 12b,12c‐Homo Derivative. An ESR and ENDOR study
inferredcites →https://doi.org/10.1002/jcc.22885openalex-snapshot
Multiwfn: A multifunctional wavefunction analyzer
inferredcites →https://doi.org/10.1016/j.cclet.2012.10.003openalex-snapshot
Fluphenazine hydrochloride radical cation assay: A new, rapid and precise method to determine in vitro total antioxidant capacity of fruit extracts
inferredcites →https://doi.org/10.1016/j.cclet.2016.06.014openalex-snapshot
BN-embedded aromatics for optoelectronic applications
inferredcites →https://doi.org/10.1016/j.cclet.2017.09.038openalex-snapshot
Recent advances in the design of dopant-free hole transporting materials for highly efficient perovskite solar cells
inferredcites →https://doi.org/10.1021/acs.accounts.8b00140openalex-snapshot
Toward Negatively Curved Carbons
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00076openalex-snapshot
Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds: Synthetic Routes, Properties, and Applications
inferredcites →https://doi.org/10.1021/acs.joc.5b01559openalex-snapshot
Scholl Cyclizations of Aryl Naphthalenes: Rearrangement Precedes Cyclization
inferredcites →https://doi.org/10.1021/acs.joc.6b01798openalex-snapshot
Regioselectivity in the Controversial Scholl Reaction of 1-Benzoylpyrene: Formation of a Five-Member Ring Is Not Unexpected
inferredcites →https://doi.org/10.1021/acs.orglett.0c02305openalex-snapshot
Condensed Phenoxazine Dimer and Its Radical Cation
inferredcites →https://doi.org/10.1021/acs.orglett.8b04059openalex-snapshot
Synthesis of a Double-Helical Naphthotetraindole Core via an Intramolecular Dehydrogenative Homocoupling Reaction
inferredcites →https://doi.org/10.1021/ar500278wopenalex-snapshot
Unconventional, Chemically Stable, and Soluble Two-Dimensional Angular Polycyclic Aromatic Hydrocarbons: From Molecular Design to Device Applications
inferredcites →https://doi.org/10.1021/cr0300901openalex-snapshot
Anisotropy of the Induced Current Density (ACID), a General Method To Quantify and Visualize Electronic Delocalization
inferredcites →https://doi.org/10.1021/cr100380zopenalex-snapshot
Semiconducting π-Conjugated Systems in Field-Effect Transistors: A Material Odyssey of Organic Electronics
inferredcites →https://doi.org/10.1021/cr500023copenalex-snapshot
Electrochemistry of Graphene and Related Materials
inferredcites →https://doi.org/10.1021/ja036732jopenalex-snapshot
Nanosized Molecular Propellers by Cyclodehydrogenation of Polyphenylene Dendrimers
inferredcites →https://doi.org/10.1021/ja046513dopenalex-snapshot
A Slippery Slope: Mechanistic Analysis of the Intramolecular Scholl Reaction of Hexaphenylbenzene
inferredcites →https://doi.org/10.1021/jacs.8b06079openalex-snapshot
Synthesis, Structures, and Properties of Core-Expanded Azacoronene Analogue: A Twisted π-System with Two N-Doped Heptagons
inferredcites →https://doi.org/10.1021/jacs.9b04080openalex-snapshot
Open-Shell and Antiaromatic Character Induced by the Highly Symmetric Geometry of the Planar Heptalene Structure: Synthesis and Characterization of a Nonalternant Isomer of Bisanthene
inferredcites →https://doi.org/10.1021/ol060333mopenalex-snapshot
Direct Synthesis of Bipyrroles Using Phenyliodine Bis(trifluoroacetate) with Bromotrimethylsilane
inferredcites →https://doi.org/10.1021/ol200069copenalex-snapshot
Sequential Oxidative Transformation of Tetraarylethylenes to 9,10-Diarylphenanthrenes and Dibenzo[g,p]chrysenes using DDQ as an Oxidant
inferredcites →https://doi.org/10.1038/s41598-018-35839-wopenalex-snapshot
Antiaromatic character of cycloheptatriene-bis-annelated indenofluorene framework mainly originated from heptafulvene segment
inferredcites →https://doi.org/10.1039/c5cp06471fopenalex-snapshot
Magnetic resonance energy and topological resonance energy
inferredcites →https://doi.org/10.1039/c7cs00508copenalex-snapshot
Recent advances in spirocyclization of indole derivatives
inferredcites →https://doi.org/10.1039/c8cc09448aopenalex-snapshot
Computational and experimental studies on the index of antiaromaticity for 4 n π-systems ( n ≥ 2)
inferredcites →https://doi.org/10.1039/c8cs00454dopenalex-snapshot
Metamorphosis of cycloalkenes for the divergent total synthesis of polycyclic indole alkaloids
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4651172openalex-extracted
Synthesis of Cyanated Naphthalene Diimide−Hydroazaacenes: Amphoteric-Redox, Low-Lying Lumo, Bright-Red Emission, Aggregation and Aromaticity Evaluation
inferred← citeshttps://doi.org/10.1002/ange.202410759openalex-snapshot
Non‐Alternant Nanographenes Bearing N‐Doped Non‐Hexagonal Pairs: Synthesis, Structural Analysis and Photophysical Properties
inferred← citeshttps://doi.org/10.1002/ange.202508785openalex-snapshot
Polycyclic Heteroaromatics with Planar‐Curved Hybrid Skeletons for High‐Performance Photocatalytic Hydrogen Peroxide Evolution
inferred← citeshttps://doi.org/10.1002/anie.202410759openalex-snapshot
Non‐Alternant Nanographenes Bearing N‐Doped Non‐Hexagonal Pairs: Synthesis, Structural Analysis and Photophysical Properties
inferred← citeshttps://doi.org/10.1002/anie.202508785openalex-snapshot
Polycyclic Heteroaromatics with Planar‐Curved Hybrid Skeletons for High‐Performance Photocatalytic Hydrogen Peroxide Evolution
inferred← citeshttps://doi.org/10.1016/j.dyepig.2024.111955openalex-snapshot
Synthesis of cyanated Naphthalene diimide−Hydroazaacenes: Amphoteric-redox, low-lying LUMO, bright-red emission, aggregation and aromaticity evaluation
inferred← citeshttps://doi.org/10.1039/d2ra05849aopenalex-snapshot
Synthesis of 5-aryl-3,3′-bis-indolyl and bis-7-aza-indolyl methanone derivatives from 5-bromo-7-azaindoles via sequential methylenation using microwave irradiation, CAN oxidation, and Suzuki coupling reactions
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