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Role of cyanuric chloride in organic synthesis: A concise overview

https://doi.org/10.1002/jhet.4661
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-3773(20011015)40:20<3726::aid-anie3726>3.0.co;2-dopenalex-snapshot
Enantioselective Organocatalysis
inferredcites →https://doi.org/10.1002/adsc.200404163openalex-snapshot
Organocatalysis: A Complementary Catalysis Strategy Advances Organic Synthesis
inferredcites →https://doi.org/10.1002/adsc.201700260openalex-snapshot
A Sequential Suzuki Coupling Approach to Unsymmetrical Aryl s‐Triazines from Cyanuric Chloride
inferredcites →https://doi.org/10.1002/anie.196306551openalex-snapshot
Syntheses of s‐Triazine and Substituted s‐Triazines
inferredcites →https://doi.org/10.1002/anie.200400650openalex-snapshot
In the Golden Age of Organocatalysis
inferredcites →https://doi.org/10.1002/cmdc.201800119openalex-snapshot
The Current Status of O‐Heterocycles: A Synthetic and Medicinal Overview
inferredcites →https://doi.org/10.1002/ejoc.202000117openalex-snapshot
Palladium‐Catalyzed Cyanation of Aryl Halides Using Formamide and Cyanuric Chloride as a New “CN” Source
inferredcites →https://doi.org/10.1002/jccs.200800141openalex-snapshot
Synthesis of Polysubstituted Quinolines Using Cyanuric Chloride as a Catalyst Under Aqueous Conditions
inferredcites →https://doi.org/10.1002/slct.202004540openalex-snapshot
Novel Annulation of Cyanuric Chloride with 2‐Aminobenzamides: A New Approach to 2‐Amino‐3‐substituted Quinazolin‐4(3 H )‐ones
inferredcites →https://doi.org/10.1007/bf03245892openalex-snapshot
Cyanuric chloride catalysed rapid conversion of β-ketoesters into β-enaminoesters under mild and solvent-free conditions
inferredcites →https://doi.org/10.1007/s10311-021-01232-9openalex-snapshot
Green synthesis of biologically active heterocycles of medicinal importance: a review
inferredcites →https://doi.org/10.1007/s11094-022-02729-5openalex-snapshot
Cyanuric Chloride Mediated One-Pot Three-Component Reaction of Benzoylhydrazinyl-N-Alkyl Acetamide Derivatives as a New Urease Inhibitor Scaffold: Docking Study and Enzyme Inhibitory Activity
inferredcites →https://doi.org/10.1007/s11705-022-2232-5openalex-snapshot
Floret-like Fe-Nx nanoparticle-embedded porous carbon superstructures from a Fe-covalent triazine polymer boosting oxygen electroreduction
inferredcites →https://doi.org/10.1007/s12039-013-0422-xopenalex-snapshot
Synthesis of spiro[pyrazolo[3,4-b] pyridine-4,3′-indoline] and spiro [benzo[h]pyrazolo[3,4-b]quinoline-4,3′-indoline] derivatives using wet cyanuric chloride under solvent-free conditionS
inferredcites →https://doi.org/10.1016/j.apcatb.2022.122067openalex-snapshot
In-situ self-templating construction of FeNi/N co-doped 3D porous carbon from bimetallic ions-coordinated porous organic polymer for rechargeable zinc-air batteries
inferredcites →https://doi.org/10.1016/j.arabjc.2017.09.016openalex-snapshot
A review on multi-component green synthesis of N-containing heterocycles using mixed oxides as heterogeneous catalysts
inferredcites →https://doi.org/10.1016/j.arabjc.2018.06.005openalex-snapshot
Multifunctionalization of cyanuric chloride for the stepwise synthesis of potential multimodal imaging chemical entities
inferredcites →https://doi.org/10.1016/j.catcom.2007.01.007openalex-snapshot
Wet cyanuric chloride catalyzed simple and efficient synthesis of 14-aryl or alkyl-14-H-dibenzo[a,j]xanthenes
inferredcites →https://doi.org/10.1016/j.cclet.2011.01.020openalex-snapshot
Cyanuric chloride-catalyzed synthesis of 10-aryl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-diones
inferredcites →https://doi.org/10.1016/j.chroma.2020.461735openalex-snapshot
Cyanuric chloride-imidazole dendrimer functionalized nanoparticles as an adsorbent for magnetic solid phase extraction of quaternary ammonium compounds from fruit and vegetable puree based infant foods
inferredcites →https://doi.org/10.1016/j.compositesa.2022.107279openalex-snapshot
Passivation of black phosphorus by triazine-based silica coating: Hierarchical BP@SiO2-N@Co(OH)2 structure for enhanced fire safety and toughness of unsaturated polyester resins
inferredcites →https://doi.org/10.1016/j.ejmech.2006.05.013openalex-snapshot
Synthesis and antibacterial activity of various substituted s-triazines
inferredcites →https://doi.org/10.1016/j.electacta.2011.07.038openalex-snapshot
Synthesis and characterization of a new hyperbranched organic–inorganic solid polymer electrolyte with cyanuric chloride as a core element
inferredcites →https://doi.org/10.1016/j.jallcom.2022.167069openalex-snapshot
COFs-Ph@CdS S-scheme heterojunctions with photocatalytic hydrogen evolution and efficient degradation properties
inferredcites →https://doi.org/10.1016/j.jnoncrysol.2008.06.035openalex-snapshot
Extended free radical network from condensed cyanuric chloride with p-phenylenediamine: An EPR/FMR study
inferredcites →https://doi.org/10.1016/j.molstruc.2017.06.042openalex-snapshot
Facile synthesis, characterization and the anchor effect on cotton fabrics of cyanuric chloride activated carbon nanotubes
inferredcites →https://doi.org/10.1016/j.mtchem.2022.101327openalex-snapshot
Gold nanoparticles decorated covalent organic polymer as a bimodal catalyst for total water splitting and nitro compound reduction
inferredcites →https://doi.org/10.1016/j.mtchem.2023.101375openalex-snapshot
Magnetite Pd-loaded nitrogen-rich porous organic polymer as a catalyst for suzuki-miyaura coupling reaction
inferredcites →https://doi.org/10.1016/j.polymer.2010.07.039openalex-snapshot
Synthesis, structure characterization and ionic conductivity of star-branched organic–inorganic hybrid electrolytes based on cyanuric chloride, diamine-capped poly(oxyalkylene) and alkoxysilane
inferredcites →https://doi.org/10.1016/j.tet.2006.07.039openalex-snapshot
Recent applications of 2,4,6-trichloro-1,3,5-triazine and its derivatives in organic synthesis
inferredcites →https://doi.org/10.1016/j.tetlet.2009.04.068openalex-snapshot
Formation of water-soluble sulfonated azacalix[4]arenes from cyanuric chloride
inferredcites →https://doi.org/10.1016/j.tetlet.2009.09.115openalex-snapshot
Cyanuric chloride: an efficient reagent for the Lossen rearrangement
inferredcites →https://doi.org/10.1016/j.tetlet.2015.03.032openalex-snapshot
Metal free organic transformation: cyanuric chloride catalyzed synthesis of 5-substituted-1H-tetrazoles
inferredcites →https://doi.org/10.1016/j.tetlet.2017.08.074openalex-snapshot
Cyanuric chloride catalyzed metal-free mild protocol for the synthesis of highly functionalized tetrahydropyridines
inferredcites →https://doi.org/10.1016/j.tetlet.2020.152707openalex-snapshot
Beckmann rearrangement of ketoximes promoted by cyanuric chloride and dimethyl sulfoxide under a mild condition
inferredcites →https://doi.org/10.1016/s0022-0728(77)80394-xopenalex-snapshot
Cyanuric chloride as a general linking agent for the attachment of redox groups to pyrolytic graphite and metal oxide electrodes
inferredcites →https://doi.org/10.1016/s0022-0728(79)80274-0openalex-snapshot
Stable attachment of redox groups for modified electrodes via cyanuric chloride
inferredcites →https://doi.org/10.1016/s0040-4039(02)00508-7openalex-snapshot
Synthesis of acyl azides from carboxylic acids using cyanuric chloride
inferredcites →https://doi.org/10.1016/s0040-4039(99)00734-0openalex-snapshot
Mild reduction of carboxylic acids to alcohols using cyanuric chloride and sodium borohydride
inferredcites →https://doi.org/10.1016/s0091-6749(98)70025-9openalex-snapshot
Immunologic cross-reactivity between respiratory chemical sensitizers: Reactive dyes and cyanuric chloride
inferredcites →https://doi.org/10.1016/s0927-7757(00)00845-1openalex-snapshot
Adsorption of cyanuric chloride-activated polyethylene glycol on liposomes
inferredcites →https://doi.org/10.1021/acsomega.2c07661openalex-snapshot
Stabilization of Palladium-Nanoparticle-Decorated Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst in C–C Coupling Reaction
inferredcites →https://doi.org/10.1021/cr0406413openalex-snapshot
Introduction: Heterocycles
inferredcites →https://doi.org/10.1021/jo5011125openalex-snapshot
Substituted 3-E-Styryl-2H-chromenes and 3-E-Styryl-2H-thiochromenes: Synthesis, Photophysical Studies, Anticancer Activity, and Exploration to Tricyclic Benzopyran Skeleton
inferredcites →https://doi.org/10.1080/00397911.2013.816736openalex-snapshot
Review of Microwave-Assisted Synthesis of Benzo-Fused Six-MemberedN,N-Heterocycles
inferredcites →https://doi.org/10.1080/00397911.2016.1192651openalex-snapshot
Use of 2,4,6-trichloro-1,3,5-triazine (TCT) as organic catalyst in organic synthesis
inferredcites →https://doi.org/10.1080/00397919408010229openalex-snapshot
Selective Mono- or Dialkoxylation of 2,4,6-Trichloro-1,3,5-triazine in Solid-Liquid Phase Transfer Conditions
inferredcites →https://doi.org/10.1080/10406638.2019.1630653openalex-snapshot
Cyanuric Chloride Catalyzed Three Component, One Pot Synthesis of Biginelli-Type Pyrimidinone Derivatives
inferredcites →https://doi.org/10.1080/10426507.2015.1054934openalex-snapshot
Cyanuric chloride-catalyzed thioacetalization for organocatalytic synthesis of thioacetals
inferredcites →https://doi.org/10.1080/17415993.2010.521940openalex-snapshot
Cyanuric chloride-catalyzed synthesis ofN-sulfonyl imines
inferredcites →https://doi.org/10.1080/17415993.2011.572971openalex-snapshot
An efficient synthesis of 1,5-benzothiazepines in the presence of sub-stoichiometric amount of cyanuric chloride
inferredcites →https://doi.org/10.1080/17415993.2015.1035273openalex-snapshot
Synthesis of alkyl thiocyanates from alcohols using a polymer-supported thiocyanate ion promoted by cyanuric chloride/dimethylformamide
inferredcites →https://doi.org/10.1080/17518250903567253openalex-snapshot
2,4,6-Trichloro[1,3,5]triazine (TCT)-catalyzed one-pot Mannich-type reaction: three component synthesis of β-amino carbonyl compounds
inferredcites →https://doi.org/10.1080/17518251003776885openalex-snapshot
Synthesis of β-amino alcohols by ring opening of epoxides with amines catalyzed by cyanuric chloride under mild and solvent-free conditions
inferredcites →https://doi.org/10.1111/cote.12631openalex-snapshot
Synthesis and properties of poly(styrene‐co‐maleic acid) macromolecular reactive dyes
inferredcites →https://doi.org/10.2174/0929867323666160809093930openalex-snapshot
A Comprehensive Review of N-Heterocycles as Cytotoxic Agents
inferredcites →https://doi.org/10.2174/1389557520666200729160720openalex-snapshot
The Chemistry of Triazine Isomers: Structures, Reactions, Synthesis and Applications
inferredcites →https://doi.org/10.22159/ajpcr.2017.v10i2.15673openalex-snapshot
A REVIEW: ANTIMICROBIAL AGENTS BASED ON NITROGEN AND SULFUR CONTAINING HETEROCYCLES
inferredcites →https://doi.org/10.3390/molecules28041941openalex-snapshot
A Promising 1,3,5-Triazine-Based Anion Exchanger for Perrhenate Binding: Crystal Structures of Its Chloride, Nitrate and Perrhenate Salts
inferredcites →https://doi.org/10.3762/bjoc.9.140openalex-snapshot
Mild and efficient cyanuric chloride catalyzed Pictet–Spengler reaction

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/14356007.a08_191.pub2openalex-snapshot
Cyanuric Acid and Cyanuric Chloride
inferred← citeshttps://doi.org/10.1002/jhet.70211openalex-snapshot
2,4,6‐Trichloro‐1,3,5‐Triazine: N , N ‐Dimethylformamide ( TCT: DMF ) Adduct as a Green Efficient Reagent for Synthetic Chemistry
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inferred← citeshttps://doi.org/10.1016/j.carbpol.2025.124826openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envpol.2024.123472openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146889openalex-snapshot
Development of triazine-piperazine hybrids as a novel class of anticancer agents: Synthesis, biological evaluation, and in silico insights
inferred← citeshttps://doi.org/10.1016/j.polymdegradstab.2025.111470openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103156openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2025.135005openalex-snapshot
TCT promoted efficient synthesis of N-sulfonyl (form)amidines from sulfonamides and (form)amides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02918openalex-snapshot
Impact of Solvent and Protonation State on Rotational Barriers in [s]-Triazines
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.5c00760openalex-snapshot
Discovery of Triazine-Based Toll-Like Receptor 9 Antagonists with Oral Activity
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5c03275openalex-snapshot
Sustainable Leather Processing: pH-Driven in Situ Self-Assembly of Biomass-Based Tanning Agents from Tea Polyphenols
inferred← citeshttps://doi.org/10.1039/d4ma00739eopenalex-snapshot
Cyanuric chloride as a linker towards the synthesis of covalent triazine polymers: a review
inferred← citeshttps://doi.org/10.1039/d4ob00683fopenalex-snapshot
Sequential nucleophilic aromatic substitutions on cyanuric chloride: synthesis of BODIPY derivatives and mechanistic insights
inferred← citeshttps://doi.org/10.1039/d5ra05849jopenalex-snapshot
A bibliometric review of triazine hybrids: synthesis, reactions, and applications spanning the last quarter-century (2000–2025)
inferred← citeshttps://doi.org/10.1039/d6cc04081kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d6ra00615aopenalex-snapshot
Recent advances in the synthesis and applications of cyanuric acid and its related analogues: a comprehensive review
inferred← citeshttps://doi.org/10.1134/s0010508225700352openalex-snapshot
Kinetic Aspects of High-Temperature Transformations of Azido-Acetylenic Derivatives of s-Triazine
inferred← citeshttps://doi.org/10.1155/joch/4469525openalex-snapshot
New s ‐Triazine–Hydrazone Hybrids Targeting EGFR: Design and Anticancer Activity Against A549 Lung Adenocarcinoma
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