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Copper-Catalyzed Double C–S Bonds Formation via Different Paths: Synthesis of Benzothiazoles from N-Benzyl-2-iodoaniline and Potassium Sulfide

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

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

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inferred← citeshttps://doi.org/10.1021/acs.joc.4c01611openalex-snapshot

Synthesis of Aryl Alkyl Thioethers via a Copper-Catalyzed Three-Component Reaction with DABSO, Aryldiazonium Salts, and Alkyl Bromides

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00288openalex-snapshot

Dual Roles of β-Oxodithioesters in the Copper-Catalyzed Synthesis of Benzo[e]pyrazolo[1,5-c][1,3]thiazine Derivatives

inferred← citeshttps://doi.org/10.1021/acs.joc.5b01602openalex-snapshot

Ammonium Iodide Induced Nonradical Regioselective Sulfenylation of Flavones via a C–H Functionalization Process

inferred← citeshttps://doi.org/10.1021/acs.joc.6b00692openalex-snapshot

Catalytic Sulfur-Enabled Dehydrobicyclization of 1,6-Enynes toward Arylated Indeno[1,2-c]thiophenes

inferred← citeshttps://doi.org/10.1021/acs.joc.6b02740openalex-snapshot

Domino Synthesis of Thiochromenes through Cu-Catalyzed Incorporation of Sulfur Using Xanthate Surrogate

inferred← citeshttps://doi.org/10.1021/acs.joc.6b02943openalex-snapshot

Copper-Catalyzed C(sp3)–S Bond and C(sp2)–S Bond Cross-Coupling of 2-(2-Iodobenzoyl) Substituted or 2-(2-Iodobenzyl) Substituted 1,2,3,4-Tetrahydroisoquinolines with Potassium Sulfide: Synthesis of Isoquinoline-Fused 1,3-Benzothiazine Scaffolds

inferred← citeshttps://doi.org/10.1021/acs.joc.7b03118openalex-snapshot

Selective Construction of 2-Substituted Benzothiazoles from o-Iodoaniline Derivatives S8 and N-Tosylhydrazones

inferred← citeshttps://doi.org/10.1021/acs.joc.9b03154openalex-snapshot

Iodine-Catalyzed Three-Component Cascade Reaction for the Synthesis of Substituted 2-Phenylnaphtho[1,3]selenazoles under Transition-Metal-Free Conditions

inferred← citeshttps://doi.org/10.1021/acs.joc.9b03489openalex-snapshot

Copper-Catalyzed Three-Component Redox-Neutral Ring Opening of Benzothiazoles to 1-Amino-N-(2-(phenylthio)phenyl)methanimine

inferred← citeshttps://doi.org/10.1021/acs.organomet.4c00330openalex-snapshot

Iron-Catalyzed Synthesis of Ferrocenyl–Thioether Conjugates via C–S Cross-Coupling of Thioethers and Vinylic Chlorides: Construction, Anticancer, and Computational Studies

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00994openalex-snapshot

K2S as Sulfur Source and DMSO as Carbon Source for the Synthesis of 2-Unsubstituted Benzothiazoles

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00079openalex-snapshot

Elemental Sulfur Mediated Decarboxylative Redox Cyclization Reaction of o-Chloronitroarenes and Arylacetic Acids

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00337openalex-snapshot

Direct ortho-Thiolation of Arenes and Alkenes by Nickel Catalysis

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02977openalex-snapshot

Copper-Catalyzed Domino Synthesis of 2-Arylthiochromanones through Concomitant C–S Bond Formations Using Xanthate as Sulfur Source

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03078openalex-snapshot

Transition-Metal-Free Sulfuration/Annulation of Alkenes: Economical Access to Thiophenes Enabled by the Cleavage of Multiple C–H Bonds

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01990openalex-snapshot

Synthesis of N -Formyl-2-benzoyl Benzothiazolines, 2-Substituted Benzothiazoles, and Symmetrical Disulfides from N -Phenacylbenzothiazolium Bromides

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02837openalex-snapshot

Di-tert-butyl Peroxide-Mediated Radical C(sp2/sp3)–S Bond Cleavage and Group-Transfer Cyclization

inferred← citeshttps://doi.org/10.1021/acsomega.0c01150openalex-snapshot

Catalyst- and Additive-Free Method for the Synthesis of 2-Substituted Benzothiazoles from Aromatic Amines, Aliphatic Amines, and Elemental Sulfur

inferred← citeshttps://doi.org/10.1021/acsomega.1c03410openalex-snapshot

Chemoselective Ullmann Reaction of α-Trisubstituted Thioamides: Synthesis of Novel 2-Iminobenzothiolanes

inferred← citeshttps://doi.org/10.1021/cr500410yopenalex-snapshot

Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles

inferred← citeshttps://doi.org/10.1021/jo501216hopenalex-snapshot

Organocatalytic Syntheses of Benzoxazoles and Benzothiazoles using Aryl Iodide and Oxone via C–H Functionalization and C–O/S Bond Formation

inferred← citeshttps://doi.org/10.1021/ol501752fopenalex-snapshot

Ambidextrous Catalytic Access to Dithieno[3,2-b:2′,3′-d]thiophene (DTT) Derivatives by Both Palladium-Catalyzed C–S and Oxidative Dehydro C–H Coupling

inferred← citeshttps://doi.org/10.1021/ol5025162openalex-snapshot

Sulfur Incorporation: Copper-Catalyzed Cascade Cyclization of 1,7-Enynes with Metal Sulfides toward Thieno[3,4-c]quinolin-4(5H)-ones

inferred← citeshttps://doi.org/10.1021/ol503186wopenalex-snapshot

Copper-Catalyzed Three-Component Synthesis of Benzothiazolethiones from o-Iodoanilines, Isocyanide, and Potassium Sulfide

inferred← citeshttps://doi.org/10.1039/c4cc08370aopenalex-snapshot

Palladium-catalyzed benzothieno[2,3-b]indole formation via dehydrative–dehydrogenative double C–H sulfuration using sulfur powder, indoles and cyclohexanones

inferred← citeshttps://doi.org/10.1039/c4cs00239copenalex-snapshot

Recent advances in C–S bond formation via C–H bond functionalization and decarboxylation

inferred← citeshttps://doi.org/10.1039/c4gc02156hopenalex-snapshot

Convenient synthesis of benzo[4,5]thiazolo[2,3-c][1,2,4]triazoles with 1 mol% CuCl 2 ·2H 2 O as catalyst in water

inferred← citeshttps://doi.org/10.1039/c4ra04047copenalex-snapshot

Copper-catalyzed synthesis of 2-aminobenzothiazoles from carbodiimide and sodium hydrosulfide

inferred← citeshttps://doi.org/10.1039/c5ob00742aopenalex-snapshot

Tetrabutylammonium iodide-catalyzed oxidative coupling of enamides with sulfonylhydrazides: synthesis of β-keto-sulfones

inferred← citeshttps://doi.org/10.1039/c5ob02193fopenalex-snapshot

Iodine-catalyzed thiolation of electron-rich aromatics using sulfonyl hydrazides as sulfenylation reagents

inferred← citeshttps://doi.org/10.1039/c5ob02619aopenalex-snapshot

Sulfuration of the C(sp 2 )–H bond of enaminones: a protocol for the synthesis of thioether using elemental sulfur as a sulfurating reagent

inferred← citeshttps://doi.org/10.1039/c5ob02670aopenalex-snapshot

Implications of dynamic imine chemistry for the sustainable synthesis of nitrogen heterocycles via transimination followed by intramolecular cyclisation

inferred← citeshttps://doi.org/10.1039/c5ra01342aopenalex-snapshot

Regioselective copper-catalyzed thiolation of imidazo[1,2-a]pyridines: an efficient C–H functionalization strategy for C–S bond formation

inferred← citeshttps://doi.org/10.1039/c5ra20405dopenalex-snapshot

Oxidative cross coupling reaction mediated by I 2 /H 2 O 2 : a novel approach for the construction of fused thiazole containing coumarin derivatives

inferred← citeshttps://doi.org/10.1039/c5ra21825jopenalex-snapshot

Synthesis and diverse general oxidative cyclization catalysis of high-valent Mo VI O 2 (HL) to ubiquitous heterocycles and their chiral analogues with high selectivity

inferred← citeshttps://doi.org/10.1039/c6ob02731hopenalex-snapshot

N-Iodosuccinimide involved one-pot metal-free synthesis of 2-heteroaromatic benzothiazole compounds

inferred← citeshttps://doi.org/10.1039/c6ra18510jopenalex-snapshot

N-Heterocyclic carbene copper( i ) complex-catalyzed synthesis of 2-aryl benzoxazoles and benzothiazoles

inferred← citeshttps://doi.org/10.1039/c7cc03273kopenalex-snapshot

Chemoselective Ullmann coupling at room temperature: a facile access to 2-aminobenzo[b]thiophenes

inferred← citeshttps://doi.org/10.1039/c7cc07366fopenalex-snapshot

Double C–S bond formation via C–H bond functionalization: synthesis of benzothiazoles and naphtho[2,1-d]thiazoles from N-substituted arylamines and elemental sulfur

inferred← citeshttps://doi.org/10.1039/c7cc09855copenalex-snapshot

Controllable assembly of the benzothiazole framework using a CC triple bond as a one-carbon synthon

inferred← citeshttps://doi.org/10.1039/c7ob02585hopenalex-snapshot

Copper-catalyzed highly selective synthesis of 2-benzyl- and 2-benzylidene-substituted benzo[ b ]thiazinones from 2-iodophenylcinnamamides and potassium sulfide

inferred← citeshttps://doi.org/10.1039/c8ob02018copenalex-snapshot

Copper-catalyzed synthesis of 2-aminophenyl benzothiazoles: a novel approach

inferred← citeshttps://doi.org/10.1039/c8ob02315hopenalex-snapshot

Copper-catalyzed synthesis of 2-acylbenzo[ b ]thiophenes from 3-(2-iodophenyl)-1-arylpropan-1-ones and potassium sulfide under aerobic conditions

inferred← citeshttps://doi.org/10.1039/d0nj05904hopenalex-snapshot

Metal-free efficient thiolation of C(sp 2 ) functionalization via in situ -generated NHTS for the synthesis of novel sulfenylated 2-aminothiazole and imidazothiazole

inferred← citeshttps://doi.org/10.1039/d0ob02320eopenalex-snapshot

Metal-catalyzed C–S bond formation using sulfur surrogates

inferred← citeshttps://doi.org/10.1039/d0ra00570copenalex-snapshot

Efficient Cu-catalyzed intramolecular O -arylation for synthesis of benzoxazoles in water

inferred← citeshttps://doi.org/10.1039/d1cc00998bopenalex-snapshot

Relieving the stress together: annulation of two different strained rings towards the formation of biologically significant heterocyclic scaffolds

inferred← citeshttps://doi.org/10.1039/d1ob01989aopenalex-snapshot

Double C–S bond formation via multiple Csp 3 –H bond cleavage: synthesis of 4-hydroxythiazoles from amides and elemental sulfur under metal-free conditions

inferred← citeshttps://doi.org/10.1039/d3qo00496aopenalex-snapshot

Applications of trisulfide radical anion S 3 ˙ − in organic synthesis

inferred← citeshttps://doi.org/10.1039/d4ob00358fopenalex-snapshot

Rapid in situ generation of 2-(halomethyl)-5-phenylfuran and nucleophilic addition in a microflow reactor

inferred← citeshttps://doi.org/10.1039/d5ob00339copenalex-snapshot

Unconventional approaches for synthesis of 2-substituted benzothiazoles

inferred← citeshttps://doi.org/10.1055/a-1914-1231openalex-snapshot

Recent Metal-Catalyzed Methods for Thioether Synthesis

inferred← citeshttps://doi.org/10.1055/a-2193-5436openalex-snapshot

An Efficient Copper-Mediated Route for the Synthesis of 2-Substituted Benzothiazoles from Dithioesters and Investigation of Their Antibacterial Activities

inferred← citeshttps://doi.org/10.1055/s-0040-1707208openalex-snapshot

Recent Advances in the Synthesis and Applications of 2-Arylbenzothiazoles

inferred← citeshttps://doi.org/10.1080/00397911.2020.1723640openalex-snapshot

Palladium acetate assisted synthesis of five-membered N- polyheterocycles

inferred← citeshttps://doi.org/10.1080/00397911.2025.2496696openalex-snapshot

Preparation of 2-( N -aroylamino)benzothiazoles via intramolecular C-S cyclization approach

inferred← citeshttps://doi.org/10.1080/10426507.2014.978323openalex-snapshot

Synthesis of Benzothiazoles by the Reaction of Disulfide and Aromatic Carboxylic Acid Promoted by PCL3 and DBU

inferred← citeshttps://doi.org/10.1080/17458080.2015.1038659openalex-snapshot

TiO2nanoparticles catalysed synthesis of 2-arylbenzimidazoles and 2-arylbenzothiazoles using hydrogen peroxide under ambient light

inferred← citeshttps://doi.org/10.14233/ajomc.2022.ajomc-p383openalex-snapshot

Recent Developments in Synthesis of Sulfur Heterocycles via Copper-Catalyzed C-S Bond Formation Reaction: A Review

inferred← citeshttps://doi.org/10.2174/1389557522666220523110521openalex-snapshot

Insight into the Synthesis, Biological Activity, and Structure-activity Relationship of Benzothiazole and Benzothiazole-hydrazone Derivatives: A Comprehensive Review

inferred← citeshttps://doi.org/10.3987/com-15-13256openalex-snapshot

Metal-Free Synthesis of Benzothiazoles from Disulfides of 2-Aminobenzenethiol and Carboxylic Acid via PCl3-Promoted Tandem Reaction

inferred← citeshttps://doi.org/10.70675/c0583415z0262z400aza0eazd18a987dbdcdopenalex-snapshot

Green construction of fused heterocycles & synthesis of carbo-benzenic phosphine derivatives

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