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The synthesis of 3,3‐dimethyl‐2‐(1‐aryl‐1h‐pyrazol‐4‐yl)‐3h‐indoles

https://doi.org/10.1002/jhet.5570430624
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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/cber.19270600118openalex-snapshot
Über die Einwirkung von Halogenphosphor auf Alkyl‐formanilide. Eine neue Methode zur Darstellung sekundärer und tertiärer p ‐Alkylamino‐benzaldehyde
inferredcites →https://doi.org/10.1002/cber.19590920811openalex-snapshot
Über α.β‐ungesättigte β‐Anilino‐carbonyl‐Verbindungen als Modellsubstanzen für den Chromophor von C‐Curarin‐III (C‐Fluorocurarin)
inferredcites →https://doi.org/10.1002/prac.19251090104openalex-snapshot
II. Über die Einwirkung von Phosphoroxychlorid auf Methyl‐ (Äthyl‐) acetanilid. Synthesen von γ‐Chlorisochinocyaninen
inferredcites →https://doi.org/10.1016/s0040-4039(99)01340-4openalex-snapshot
Pseudo Vilsmeier reagents a new protocol for regiospecific CC bond formation in pyridines
inferredcites →https://doi.org/10.1055/s-1999-3643openalex-snapshot
Synthesis of 2-Aryl- and 2-Hetaryl-4,6-dinitroindoles from 2,4,6-Trinitrotoluene
inferredcites →https://doi.org/10.1107/s1600536806002261openalex-snapshot
Formylation of an indolenine: 2-(diformylmethylidene)-3,3-dimethyl-2,3-dihydro-1H-indole

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.4648479openalex-extracted
The Effect of Π-Extended Indoleninyl-Dibenzotetraaza[14]Annulenes on the Third-Order Nonlinear Optical Properties
inferred← citeshttps://doi.org/10.1002/chin.200715112openalex-snapshot
The Synthesis of 3,3‐Dimethyl‐2‐(1‐aryl‐1H‐pyrazol‐4‐yl)‐3H‐indoles.
inferred← citeshttps://doi.org/10.1002/ejic.201402745openalex-snapshot
A Tetradentate β‐Diiminato Ligand Containing Phenolate Substituents: Flexivalent Coordination to MnIII, CoIII, NiII, and CuII
inferred← citeshttps://doi.org/10.1002/jhet.1626openalex-snapshot
The Synthesis of New Heterocycles Using 2‐(4‐Chloro‐1,3‐dihydro‐3,3,7‐trimethyl‐2H‐indol‐2‐ylidene) Propanedial
inferred← citeshttps://doi.org/10.1002/jhet.1735openalex-snapshot
Synthesis of New Heterocyclic Compounds Using 2‐(3,3‐dimethyl‐1H‐pyrroloisoquinolin‐2(3H)‐ylidene)malonaldehydes
inferred← citeshttps://doi.org/10.1002/jhet.18openalex-snapshot
The synthesis of 4‐(3,3‐dimethyl‐3H‐pyrrolo[2,3‐f]quinolin‐2‐yl)pyrazoles and 4‐(3,3‐dimethyl‐3H‐pyrrolo[3,2‐h]quinolin‐2‐yl)pyrazoles
inferred← citeshttps://doi.org/10.1002/jhet.2102openalex-snapshot
The Synthesis of 6‐Substituted Pyrido[2,3‐d]pyrimidine‐2,4(1H,3H)‐diones Using Aminomethylene Malondialdehydes and 6‐Aminouracils
inferred← citeshttps://doi.org/10.1002/jhet.2772openalex-snapshot
Indole‐Fused Epoxy‐1,5‐Diazocines as Cancer‐Selective Cytotoxic Agents
inferred← citeshttps://doi.org/10.1002/jhet.3075openalex-snapshot
A Simple and Efficient Regioselective and Chemoselective Synthesis of New Substituted 3‐Methyl‐6‐arylpyridazine‐4‐carboxamides and 5‐Oxo‐3‐aryl‐5,6‐dihydropyrido[4,3‐c]pyridazine‐8‐carbaldehydes
inferred← citeshttps://doi.org/10.1002/jhet.575openalex-snapshot
Reactions of 2‐(diformylmethylidene)‐3,3‐dimethylindole with hydrazides: Synthesis of new pyrazolylindolenine derivatives—the unprecedented one‐pot pyrazole–thiadiazole double annulation
inferred← citeshttps://doi.org/10.1007/s11030-023-10662-2openalex-snapshot
Structural insights and cytotoxicity evaluation of benz[e]indole pyrazolyl-substituted amides
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107256openalex-snapshot
Discovery of indoleninyl-pyrazolo[3,4-b]pyridines as potent chemotherapeutic agents against colorectal cancer cells
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138066openalex-snapshot
The effect of π-extended indoleninyl-dibenzotetraaza[14]annulenes on their third-order nonlinear optical properties
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.084openalex-snapshot
Synthesis of substituted 2-heteroarylbenzazol-5-ol derivatives as potential ligands for estrogen receptors
inferred← citeshttps://doi.org/10.1016/j.tet.2014.01.070openalex-snapshot
Synthesis of new fluorescent building blocks via the microwave-assisted annulation reaction of 1,1,2-trimethyl-1H-benzo[e]indole with acrylic acid and its derivatives
inferred← citeshttps://doi.org/10.1039/d0nj04357eopenalex-snapshot
Supramolecular assembly and spectroscopic characterization of indolenine–barbituric acid zwitterions
inferred← citeshttps://doi.org/10.1080/14786419.2022.2101052openalex-snapshot
Potential antiplatelet aggregation metabolites from the discarded sorghum (Sorghum bicolor L.) root
inferred← citeshttps://doi.org/10.1107/s1600536809038495openalex-snapshot
A second monoclinic polymorph of 2-(diformylmethylidene)-3,3-dimethyl-2,3-dihydro-1H-indole
inferred← citeshttps://doi.org/10.1107/s1600536809052581openalex-snapshot
7-Chloro-2-[1-(4-methoxyphenyl)pyrazol-4-yl]-3,3-dimethyl-3H-indole
inferred← citeshttps://doi.org/10.1107/s1600536811053906openalex-snapshot
2-[(Z)-4,7-Dichloro-3,3-dimethyl-2,3-dihydro-1H-indol-2-ylidene]-3-oxopropanenitrile
inferred← citeshttps://doi.org/10.1107/s1600536811053918openalex-snapshot
2-(4-Chloro-3,3,7-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-2-cyanoacetamide
inferred← citeshttps://doi.org/10.1515/zkri-2025-0051openalex-snapshot
Exploring the molecular characteristics of a benzoindoleninyl-pyrazolo[3,4- b ]pyridine
inferred← citeshttps://doi.org/10.29409/cfswjb94openalex-snapshot
Synthesis, characterization and cytotoxic effect of 2-((E)-((E)-2-(5-chloro-3,3-dimethylindolin-2-ylidene)-3-oxopropylidene) amino) benzoic acid on the MCF7 cancer cell line
inferred← citeshttps://doi.org/10.3390/molecules26133897openalex-snapshot
5-(Indol-2-yl)pyrazolo[3,4-b]pyridines as a New Family of TASK-3 Channel Blockers: A Pharmacophore-Based Regioselective Synthesis
inferred← citeshttps://doi.org/10.5267/j.ccl.2012.10.001openalex-snapshot
Synthesis of new heterocyclic compounds using 2-(4,7-dichloro-3,3-dimethyl-indolin-2-ylidene)malonaldehyde
inferred← citeshttps://doi.org/10.5267/j.ccl.2013.07.003openalex-snapshot
Vilsmeier-Haack reagent: A facile synthesis of 2-(4-chloro-3,3-dimethyl-7-phenoxyindolin-2-ylidene)malonaldehyde and transformation into different heterocyclic compounds
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