On the public citation graph

One-Pot Reaction between N-Tosylhydrazones and 2-Nitrobenzyl Bromide: Route to NH-Free C2-Arylindoles

https://doi.org/10.1021/acs.joc.8b02623

0 signed · 100 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/adsc.201000512openalex-snapshot

“On Water” Direct and Site‐Selective Pd‐Catalysed CH Arylation of (NH)‐Indoles

inferredcites →https://doi.org/10.1002/adsc.201300466openalex-snapshot

Copper Acetoacetonate [Cu(acac)2]/BINAP‐Promoted Csp3N Bond Formation via Reductive Coupling of N‐Tosylhydrazones with Anilines

inferredcites →https://doi.org/10.1002/ajoc.201500289openalex-snapshot

Transition‐Metal‐Free Synthesis of Polysubstituted Cyclopropane Derivatives from N‐Tosylhydrazones and their Cytotoxic Activities

inferredcites →https://doi.org/10.1002/anie.200701815openalex-snapshot

N ‐Tosylhydrazones as Reagents for Cross‐Coupling Reactions: A Route to Polysubstituted Olefins

inferredcites →https://doi.org/10.1002/anie.201001704openalex-snapshot

Straightforward Synthesis of Ethers: Metal‐Free Reductive Coupling of Tosylhydrazones with Alcohols or Phenols

inferredcites →https://doi.org/10.1002/anie.201007961openalex-snapshot

Tosylhydrazones: New Uses for Classic Reagents in Palladium‐Catalyzed Cross‐Coupling and Metal‐Free Reactions

inferredcites →https://doi.org/10.1002/anie.201103014openalex-snapshot

Umpolung Reactivity of Indole through Gold Catalysis

inferredcites →https://doi.org/10.1002/anie.201508818openalex-snapshot

Scaffold Diversity Synthesis and Its Application in Probe and Drug Discovery

inferredcites →https://doi.org/10.1002/cctc.200900074openalex-snapshot

Palladium‐Catalyzed C3 or C4 Direct Arylation of Heteroaromatic Compounds with Aryl Halides by CH Bond Activation

inferredcites →https://doi.org/10.1002/cmdc.200900290openalex-snapshot

Synthesis, Biological Evaluation of 1,1‐Diarylethylenes as a Novel Class of Antimitotic Agents

inferredcites →https://doi.org/10.1002/ejoc.201001492openalex-snapshot

Synthesis of Sulfones by Iron‐Catalyzed Decomposition of Sulfonylhydrazones

inferredcites →https://doi.org/10.1007/s00044-016-1543-9openalex-snapshot

Synthesis and antimicrobial evaluation of hydrazones derived from 4-methylbenzenesulfonohydrazide in aqueous medium

inferredcites →https://doi.org/10.1016/j.bmcl.2009.07.091openalex-snapshot

The synthesis of 2- and 3-aryl indoles and 1,3,4,5-tetrahydropyrano[4,3-b]indoles and their antibacterial and antifungal activity

inferredcites →https://doi.org/10.1016/j.ejmech.2017.04.003openalex-snapshot

Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

inferredcites →https://doi.org/10.1016/j.jcat.2017.06.021openalex-snapshot

Enhancement of gold catalytic activity and stability by immobilization on the surface of graphene

inferredcites →https://doi.org/10.1016/j.tet.2011.07.056openalex-snapshot

Solvent-free synthesis of hydrazones and their subsequent N-alkylation in a Ball-mill

inferredcites →https://doi.org/10.1016/j.tetlet.2017.04.066openalex-snapshot

Palladium-catalyzed direct C2-arylation of free (N H) indoles via norbornene-mediated regioselective C H activation

inferredcites →https://doi.org/10.1016/s0022-328x(00)82974-5openalex-snapshot

Purification of Laboratory Chemicals

inferredcites →https://doi.org/10.1016/s0040-4039(99)01080-1openalex-snapshot

Synthesis of indoles: selenium-catalyzed reductive N-heterocyclization of 2-nitrostyrenes with carbon monoxide

inferredcites →https://doi.org/10.1021/acs.joc.5b00500openalex-snapshot

Palladium-Catalyzed Tandem Carbene Migratory Insertion and Intramolecular Cyclization: Synthesis of Chromeno[4,3-b]chromene Compounds

inferredcites →https://doi.org/10.1021/acs.joc.7b00148openalex-snapshot

The Development of a Palladium-Catalyzed Tandem Addition/Cyclization for the Construction of Indole Skeletons

inferredcites →https://doi.org/10.1021/acs.joc.7b02728openalex-snapshot

Palladium-Catalyzed Sequential Vinylic C–H Arylation/Amination of 2-Vinylanilines with Aryl boronic Acids: Access to 2-Arylindoles

inferredcites →https://doi.org/10.1021/acs.organomet.6b00879openalex-snapshot

Developing P-Stereogenic, Planar–Chiral P-Alkene Ligands: Monodentate, Bidentate, and Double Agostic Coordination Modes on Ru(II)

inferredcites →https://doi.org/10.1021/acs.orglett.7b00101openalex-snapshot

One-Pot Acid-Catalyzed Ring-Opening/Cyclization/Oxidation of Aziridines with N -Tosylhydrazones: Access to 1,2,4-Triazines

inferredcites →https://doi.org/10.1021/acs.orglett.7b00613openalex-snapshot

Pd-Catalyzed Autotandem Reactions with N-Tosylhydrazones. Synthesis of Condensed Carbo- and Heterocycles by Formation of a C–C Single Bond and a C═C Double Bond on the Same Carbon Atom

inferredcites →https://doi.org/10.1021/acs.orglett.7b03422openalex-snapshot

Csp2–Csp2 and Csp2–N Bond Formation in a One-Pot Reaction between N-Tosylhydrazones and Bromonitrobenzenes: An Unexpected Cyclization to Substituted Indole Derivatives

inferredcites →https://doi.org/10.1021/co500115bopenalex-snapshot

Synthesis of a 3-(α-Styryl)benzo[ b ]-thiophene Library via Bromocyclization of Alkynes and Palladium-Catalyzed Tosylhydrazones Cross-Couplings: Evaluation as Antitubulin Agents

inferredcites →https://doi.org/10.1021/cr0201068openalex-snapshot

Transition-Metal-Catalyzed Addition of Heteroatom−Hydrogen Bonds to Alkynes

inferredcites →https://doi.org/10.1021/cs5014877openalex-snapshot

Copper-Catalyzed Coupling of N-Tosylhydrazones with Amines: Synthesis of Fluorene Derivatives

inferredcites →https://doi.org/10.1021/ja029573xopenalex-snapshot

Generation of Phosphoranes Derived from Phosphites. A New Class of Phosphorus Ylides Leading to High E Selectivity with Semi-stabilizing Groups in Wittig Olefinations

inferredcites →https://doi.org/10.1021/ja034606+openalex-snapshot

A New Protocol for the In Situ Generation of Aromatic, Heteroaromatic, and Unsaturated Diazo Compounds and Its Application in Catalytic and Asymmetric Epoxidation of Carbonyl Compounds. Extensive Studies To Map Out Scope and Limitations, and Rationalization of Diastereo- and Enantioselectivities

inferredcites →https://doi.org/10.1021/ja050279popenalex-snapshot

Direct C-Arylation of Free (NH)-Indoles and Pyrroles Catalyzed by Ar−Rh(III) Complexes Assembled In Situ

inferredcites →https://doi.org/10.1021/ja0745862openalex-snapshot

Elements of Regiocontrol in Palladium-Catalyzed Oxidative Arene Cross-Coupling

inferredcites →https://doi.org/10.1021/ja710731aopenalex-snapshot

Room Temperature and Phosphine Free Palladium Catalyzed Direct C-2 Arylation of Indoles

inferredcites →https://doi.org/10.1021/jm3013097openalex-snapshot

Toward Highly Potent Cancer Agents by Modulating the C‑2 Group of the Arylthioindole Class of Tubulin Polymerization Inhibitors

inferredcites →https://doi.org/10.1021/jm900321uopenalex-snapshot

Isocombretastatins A versus Combretastatins A: The Forgotten isoCA-4 Isomer as a Highly Promising Cytotoxic and Antitubulin Agent

inferredcites →https://doi.org/10.1021/jo2018119openalex-snapshot

Gold(I)-Catalyzed Polycyclizations of Polyenyne-Type Anilines Based on Hydroamination and Consecutive Hydroarylation Cascade

inferredcites →https://doi.org/10.1021/jo202598eopenalex-snapshot

Synthesis of Substituted 1H-Indazoles from Arynes and Hydrazones

inferredcites →https://doi.org/10.1021/jo702423zopenalex-snapshot

A Ceric Ammonium Nitrate N-Dearylation of N-p-Anisylazoles Applied to Pyrazole, Triazole, Tetrazole, and Pentazole Rings: Release of Parent Azoles. Generation of Unstable Pentazole, HN5/N5-, in Solution

inferredcites →https://doi.org/10.1021/jo800464uopenalex-snapshot

InBr3-Promoted Divergent Approach to Polysubstituted Indoles and Quinolines from 2-Ethynylanilines: Switch from an Intramolecular Cyclization to an Intermolecular Dimerization by a Type of Terminal Substituent Group

inferredcites →https://doi.org/10.1021/jo801371wopenalex-snapshot

Palladium-Catalyzed Direct C-2 Arylation of Indoles with Potassium Aryltrifluoroborate Salts

inferredcites →https://doi.org/10.1021/jo802590bopenalex-snapshot

Scope of the Suzuki−Miyaura Cross-Coupling Reactions of Potassium Heteroaryltrifluoroborates

inferredcites →https://doi.org/10.1021/ol0711117openalex-snapshot

Palladium-Catalyzed C−H Activation/Intramolecular Amination Reaction: A New Route to 3-Aryl/Alkylindazoles

inferredcites →https://doi.org/10.1021/ol101147bopenalex-snapshot

Pd(OAc)2-Catalyzed Regioselective Arylation of Indoles with Arylsiloxane in Acidic Medium

inferredcites →https://doi.org/10.1021/ol101639gopenalex-snapshot

Pd-Catalyzed Reaction of Sterically Hindered Hydrazones with Aryl Halides: Synthesis of Tetra-Substituted Olefins Related to iso-Combretastatin A4

inferredcites →https://doi.org/10.1021/ol200094bopenalex-snapshot

Synthetic Studies on Indolocarbazoles: Total Synthesis of Staurosporine Aglycon

inferredcites →https://doi.org/10.1021/ol302522nopenalex-snapshot

Rhodium-Catalyzed Oxidative Annulation of Sulfonylhydrazones with Alkenes

inferredcites →https://doi.org/10.1021/ol402523xopenalex-snapshot

Traceless Directing Strategy: Efficient Synthesis of N-Alkyl Indoles via Redox-Neutral C–H Activation

inferredcites →https://doi.org/10.1021/ol901876wopenalex-snapshot

Pd-Catalyzed C═C Double-Bond Formation by Coupling of N-Tosylhydrazones with Benzyl Halides

inferredcites →https://doi.org/10.1039/b719641eopenalex-snapshot

Regiochemistry of the microwave-assisted reaction between aromatic amines and α-bromoketones to yield substituted 1H-indoles

inferredcites →https://doi.org/10.1039/c0ob00639dopenalex-snapshot

Synthesis of thioethers via metal-free reductive coupling of tosylhydrazones with thiols

inferredcites →https://doi.org/10.1039/c1cc13632aopenalex-snapshot

Regiocontrolled aerobic oxidative coupling of indoles and benzene using Pd catalysts with 4,5-diazafluorene ligands

inferredcites →https://doi.org/10.1039/c1ob05664fopenalex-snapshot

Copper-catalyzed reductive coupling of tosylhydrazones with amines: A convenient route to α-branched amines

inferredcites →https://doi.org/10.1039/c2ob26253copenalex-snapshot

Synthesis, biological evaluation, and structure–activity relationships of tri- and tetrasubstituted olefins related to isocombretastatin A-4 as new tubulin inhibitors

inferredcites →https://doi.org/10.1039/c2ob26456kopenalex-snapshot

Synthesis of 2-arylindole derivatives and evaluation as nitric oxide synthase and NFκB inhibitors

inferredcites →https://doi.org/10.1039/c2ob27125gopenalex-snapshot

2-Substituted 3-arylindoles through palladium-catalyzed arylative cyclization of 2-alkynyltrifluoroacetanilides with arylboronic acids under oxidative conditions

inferredcites →https://doi.org/10.1039/c3ob40263kopenalex-snapshot

An efficient coupling of N-tosylhydrazones with 2-halopyridines: synthesis of 2-α-styrylpyridines endowed with antitumor activity

inferredcites →https://doi.org/10.1039/c4nr00715hopenalex-snapshot

Facile preparation of Pd nanoparticles supported on single-layer graphene oxide and application for the Suzuki–Miyaura cross-coupling reaction

inferredcites →https://doi.org/10.1039/c4ra00603hopenalex-snapshot

Microwave irradiated synthesis of 2-bromo(chloro)indoles via intramolecular cyclization of 2-(gem-dibromo(chloro)vinyl)anilines in the presence of TBAF under metal-free conditions

inferredcites →https://doi.org/10.1039/c6cc07666aopenalex-snapshot

A general synthesis of arylindoles and (1-arylvinyl)carbazoles via a one-pot reaction from N-tosylhydrazones and 2-nitro-haloarenes and their potential application to colon cancer

inferredcites →https://doi.org/10.1039/c6cs00737fopenalex-snapshot

N-Tosylhydrazones: versatile synthons in the construction of cyclic compounds

inferredcites →https://doi.org/10.1039/sa9720900147openalex-snapshot

New Members of Council

inferredcites →https://doi.org/10.1055/s-0036-1588893openalex-snapshot

Synthesis of Di- and Triarylmethanes through Palladium-Catalyzed Reductive Coupling of N-Tosylhydrazones and Aryl Bromides

inferredcites →https://doi.org/10.1080/00397911.2017.1381260openalex-snapshot

Design and applications of new phosphine-free tetradentate Pd-catalyst: Regioselective C–H activation on 1-substituted 1,2,3-triazoles and indoles(NH-Free)

inferredcites →https://doi.org/10.1126/science.1141956openalex-snapshot

The Catalytic Cross-Coupling of Unactivated Arenes

inferredcites →https://doi.org/10.15227/orgsyn.064.0207openalex-snapshot

TOSYLHYDRAZONE SALT PYROLYSES: PHENYLDIAZOMETHANES

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.4598991openalex-extracted

Asymmetric Cycloadditions, Diels-Alder and Cyclopropanation Transformations, with (S)-Benzyl N-2-Trifluoroacetamidoacrylyl Oxazolidinone

inferred← citeshttps://doi.org/10.1002/0471264180.or111.02openalex-snapshot

Reductive Cyclization of 2‐Nitro‐ and β‐Nitrostyrenes, 2‐Nitrobiphenyls, and 1‐Nitro‐1,3‐Dienes to Indoles, Carbazoles, and Pyrroles

inferred← citeshttps://doi.org/10.1002/adsc.202000466openalex-snapshot

Sulfonyl Hydrazides in Organic Synthesis: A Review of Recent Studies

inferred← citeshttps://doi.org/10.1002/adsc.202300613openalex-snapshot

Synthesis of Aza‐Heterocyclic Compounds with N ‐Tosylhydrazones: Formation of Bi‐Indoles via Reductive Molybdenum Catalysis

inferred← citeshttps://doi.org/10.1002/ajoc.202300548openalex-snapshot

Palladium‐Catalyzed Synthesis of Bicyclic Derivatives from the Cyclization/1,4‐Difunctionalization of Bromoarenes with Diazo Compounds

inferred← citeshttps://doi.org/10.1002/chem.202302769openalex-snapshot

Concise Synthesis of (±)‐Fortuneicyclidins and (±)‐Cephalotine B Enabled by Pd‐Catalyzed Dearomative Spirocyclization**

inferred← citeshttps://doi.org/10.1002/ejoc.202101505openalex-snapshot

Synthesis of 2‐Substituted Indoles by Pd‐Catalyzed Reductive Cyclization of 1‐Halo‐2‐nitrobenzene with Alkynes

inferred← citeshttps://doi.org/10.1007/7081_2023_64openalex-snapshot

Heterocycles from Donor and Donor/Donor Carbenes

inferred← citeshttps://doi.org/10.1016/j.desal.2024.117594openalex-snapshot

Simultaneous selective separation and enrichment of bromine and cesium ions by electrochemically switched amphoteric ion membrane

inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112873openalex-snapshot

Cyclic bridged analogs of isoCA-4: Design, synthesis and biological evaluation

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.141926openalex-snapshot

A novel crosslinked chitosan material modified by quaternary ammonium group for efficient adsorption of bromide ions from wastewater

inferred← citeshttps://doi.org/10.1016/j.jece.2022.107946openalex-snapshot

Highly efficient recovery of bromine from shale gas wastewater by selective electrochemical oxidation

inferred← citeshttps://doi.org/10.1016/j.memsci.2025.124239openalex-snapshot

Ionic liquid-based supported liquid membranes for enhanced cesium continuous separation via crown-ether facilitated transport

inferred← citeshttps://doi.org/10.1016/j.psep.2025.107622openalex-snapshot

A novel separation process for the bromide and carbonate from the air blow-out alkali absorbed liquid and its phase equilibrium

inferred← citeshttps://doi.org/10.1016/j.tet.2021.132331openalex-snapshot

A palladium-catalyzed Barluenga cross-coupling – Reductive cyclization sequence to substituted indoles

inferred← citeshttps://doi.org/10.1016/j.tet.2025.134838openalex-snapshot

Synthesis of 2-substituted 3-acylindoles via reductive cyclization – rearrangement of β-acyl β-alkyl-substituted 2-nitrostyrenes

inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00742openalex-snapshot

The Carbene Chemistry of N -Sulfonyl Hydrazones: The Past, Present, and Future

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01835openalex-snapshot

Sequential One-Pot Synthesis of 3-Arylbenzofurans from N-Tosylhydrazones and Bromophenol Derivatives

inferred← citeshttps://doi.org/10.1021/acs.joc.0c02421openalex-snapshot

Direct Access for the Regio- and Stereoselective Synthesis of N-Alkenylpyrazoles and Chromenopyrazoles

inferred← citeshttps://doi.org/10.1021/acs.joc.1c02580openalex-snapshot

Pd-Catalyzed Coupling of N-Tosylhydrazones with Benzylic Phosphates: Toward the Synthesis of Di- or Tri-Substituted Alkenes

inferred← citeshttps://doi.org/10.1021/acs.joc.2c01574openalex-snapshot

Benzylic C(sp 3 )–H Bonds Play the Dual Role of Starting Material and Oxidation Inhibitor for Hydrazides in the Electrochemical Synthesis of Hydrazones

inferred← citeshttps://doi.org/10.1021/acs.joc.3c02676openalex-snapshot

Silver-Promoted Rapid Synthesis of 3-Arylindan-1-ones: Microwave-Assisted Reductive Coupling of N-Tosylhydrazone and Boronic Acids

inferred← citeshttps://doi.org/10.1021/acs.joc.4c01317openalex-snapshot

N–H Insertion of Anilines on N -Tosylhydrazones Induced by Visible Light Irradiation

inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01699openalex-snapshot

From Styrenes to Fluorinated Benzyl Bromides: A Photoinduced Difunctionalization via Atom Transfer Radical Addition

inferred← citeshttps://doi.org/10.1021/acscatal.9b01180openalex-snapshot

Overcoming Scope Limitations in Cross-Coupling of Diazo Nucleophiles by Manipulating Catalyst Speciation and Using Flow Diazo Generation

inferred← citeshttps://doi.org/10.1039/d0cc06236gopenalex-snapshot

Palladium-catalyzed cross-coupling reaction of sulfoxonium ylides and benzyl bromides by carbene migratory insertion

inferred← citeshttps://doi.org/10.1039/d1dt03161aopenalex-snapshot

A mechanistic investigation of the Pd-catalyzed cross-coupling between N -tosylhydrazones and aryl halides

inferred← citeshttps://doi.org/10.1039/d1ob02443dopenalex-snapshot

Regioselective synthesis of 6-nitroindole derivatives from enaminones and nitroaromatic compounds via transition metal-free C–C and C–N bond formation

inferred← citeshttps://doi.org/10.1039/d5ob00338eopenalex-snapshot

A review on indole synthesis from nitroarenes: classical to modern approaches

inferred← citeshttps://doi.org/10.2174/1385272826666220201124008openalex-snapshot

Palladium-Catalysed Intermolecular Direct C–H Bond Arylation of Heteroarenes with Reagents Alternative to Aryl Halides: Current State of the Art

inferred← citeshttps://doi.org/10.59761/rcr5167openalex-snapshot

ortho-Functionalized nitroarenes in the synthesis of heterocycles

inferred← citeshttps://doi.org/10.70675/2afd7c7bz0a8az433cza5e1z34ba26ebf1d9openalex-snapshot

Formation de liaisons C-N et C-C par photocatalyse visible

inferred← citeshttps://doi.org/10.70675/5ee153bez3730z4b9fz88b4zd2a26267a294openalex-snapshot

Synthesis of heterocycles related to indole and reactivity of TMSCl/NaI

inferred← citeshttps://doi.org/10.70675/af146110z8b0fz4a30zb66eza285a48f1d6aopenalex-snapshot

Conception, synthèse et vectorisation de molécules apparentées à l'isocombrétastatine A-4 : Exploration de nouvelles réactivites des composés diazo-précurseurs

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.