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AlAr3(THF): highly efficient reagents for cross-couplings with aryl bromides and chlorides catalyzed by the economic palladium complex of PCy3

https://doi.org/10.1039/b707703c
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-3773(20020104)41:1<179::aid-anie179>3.0.co;2-oopenalex-snapshot
A Convenient Oxime-Carbapalladacycle-Catalyzed Suzuki Cross-Coupling of Aryl Chlorides in Water
inferredcites →https://doi.org/10.1002/1521-3773(20021104)41:21<4056::aid-anie4056>3.0.co;2-8openalex-snapshot
Palladium-Catalyzed Coupling of Alkyl Chlorides and Grignard Reagents
inferredcites →https://doi.org/10.1002/1521-3773(20021104)41:21<4120::aid-anie4120>3.0.co;2-7openalex-snapshot
Simple Mixed Tricyclohexylphosphane–Triarylphosphite Complexes as Extremely High-Activity Catalysts for the Suzuki Coupling of Aryl Chlorides
inferredcites →https://doi.org/10.1002/adsc.200404188openalex-snapshot
Cross‐Coupling of Triallyl(aryl)silanes with Aryl Bromides and Chlorides: An Alternative Convenient Biaryl Synthesis
inferredcites →https://doi.org/10.1002/adsc.200505271openalex-snapshot
Remarkable Anion and Cation Effects on Stille Reactions in Functionalised Ionic Liquids
inferredcites →https://doi.org/10.1002/anie.199523711openalex-snapshot
Metal Complexes of N‐Heterocyclic Carbenes—A New Structural Principle for Catalysts in Homogeneous Catalysis
inferredcites →https://doi.org/10.1002/anie.199607251openalex-snapshot
Nucleophilic Carbenes: An Incredible Renaissance
inferredcites →https://doi.org/10.1002/anie.200300638openalex-snapshot
The Mechanisms of the Stille Reaction
inferredcites →https://doi.org/10.1002/anie.200351325openalex-snapshot
An N‐Heterocyclic Carbene Ligand with Flexible Steric Bulk Allows Suzuki Cross‐Coupling of Sterically Hindered Aryl Chlorides at Room Temperature
inferredcites →https://doi.org/10.1002/anie.200352979openalex-snapshot
Stille Coupling Made Easier—The Synergic Effect of Copper( I ) Salts and the Fluoride Ion
inferredcites →https://doi.org/10.1002/anie.200460504openalex-snapshot
Cross‐Coupling of Alkyl Halides with Aryl Grignard Reagents Catalyzed by a Low‐Valent Iron Complex
inferredcites →https://doi.org/10.1002/chin.200637047openalex-snapshot
Amino Alcohols as Ligands for Nickel‐Catalyzed Suzuki Reactions of Unactivated Alkyl Halides, Including Secondary Alkyl Chlorides with Arylboronic Acids.
inferredcites →https://doi.org/10.1016/j.tetlet.2003.09.147openalex-snapshot
Lanthanide assisted cross-coupling of aryl bromides with triethylaluminum
inferredcites →https://doi.org/10.1016/s0040-4020(01)00998-xopenalex-snapshot
Synthesis of pinacol arylboronates via cross-coupling reaction of bis(pinacolato)diboron with chloroarenes catalyzed by palladium(0)–tricyclohexylphosphine complexes
inferredcites →https://doi.org/10.1021/ar00083a001openalex-snapshot
Palladium- or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formation
inferredcites →https://doi.org/10.1021/cr000664ropenalex-snapshot
Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
inferredcites →https://doi.org/10.1021/ja0002058openalex-snapshot
Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions
inferredcites →https://doi.org/10.1021/ja00242a024openalex-snapshot
Nickel- or palladium-catalyzed cross coupling. 31. Palladium- or nickel-catalyzed reactions of alkenylmetals with unsaturated organic halides as a selective route to arylated alkenes and conjugated dienes: scope, limitations, and mechanism
inferredcites →https://doi.org/10.1021/ja00735a029openalex-snapshot
Alkylcopper(I) in the coupling of Grignard reagents with alkyl halides
inferredcites →https://doi.org/10.1021/ja00735a030openalex-snapshot
Vinylation of Grignard reagents. Catalysis by iron
inferredcites →https://doi.org/10.1021/ja016863popenalex-snapshot
An Efficient Intermolecular Palladium-Catalyzed Synthesis of Aryl Ethers
inferredcites →https://doi.org/10.1021/ja027190topenalex-snapshot
Iron-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/ja035483wopenalex-snapshot
Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions
inferredcites →https://doi.org/10.1021/ja038631ropenalex-snapshot
A General Method for the Suzuki−Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-ortho-substituted Biaryls in 2-Propanol at Room Temperature
inferredcites →https://doi.org/10.1021/ja0393729openalex-snapshot
Cross-Couplings of Alkyl Electrophiles under “Ligandless” Conditions: Negishi Reactions of Organozirconium Reagents
inferredcites →https://doi.org/10.1021/ja042491jopenalex-snapshot
Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure
inferredcites →https://doi.org/10.1021/ja0436300openalex-snapshot
Stille Cross-Couplings of Unactivated Secondary Alkyl Halides Using Monoorganotin Reagents
inferredcites →https://doi.org/10.1021/ja0450096openalex-snapshot
Highly Active Palladium Catalysts Supported by Bulky Proazaphosphatrane Ligands for Stille Cross-Coupling: Coupling of Aryl and Vinyl Chlorides, Room Temperature Coupling of Aryl Bromides, Coupling of Aryl Triflates, and Synthesis of Sterically Hindered Biaryls
inferredcites →https://doi.org/10.1021/ja050471ropenalex-snapshot
Use of Tunable Ligands Allows for Intermolecular Pd-Catalyzed C−O Bond Formation
inferredcites →https://doi.org/10.1021/ja052547popenalex-snapshot
Preferential Oxidative Addition in Palladium(0)-Catalyzed Suzuki Cross-Coupling Reactions of Dihaloarenes with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ja056327nopenalex-snapshot
Nickel-Catalyzed Cross-Coupling Reaction of Aryl Fluorides and Chlorides with Grignard Reagents under Nickel/Magnesium Bimetallic Cooperation
inferredcites →https://doi.org/10.1021/ja0613761openalex-snapshot
Amino Alcohols as Ligands for Nickel-Catalyzed Suzuki Reactions of Unactivated Alkyl Halides, Including Secondary Alkyl Chlorides, with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ja062080yopenalex-snapshot
Remarkably Efficient Enantioselective Titanium(IV)−(R)-H8-BINOLate Catalyst for Arylations to Aldehydes by Triaryl(tetrahydrofuran)aluminum Reagents
inferredcites →https://doi.org/10.1021/ja062206ropenalex-snapshot
New Mechanistic Insights Regarding Pd/Cu Catalysts for the Sonogashira Reaction: HRMAS NMR Studies of Silica-Immobilized Systems
inferredcites →https://doi.org/10.1021/ja0662467openalex-snapshot
Enantioselective Synthesis of N1999A2
inferredcites →https://doi.org/10.1021/ja067975popenalex-snapshot
Boron-Masking Strategy for the Selective Synthesis of Oligoarenes via Iterative Suzuki−Miyaura Coupling
inferredcites →https://doi.org/10.1021/ja982250+openalex-snapshot
A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides
inferredcites →https://doi.org/10.1021/ja991703nopenalex-snapshot
Efficient Cross-Coupling of Aryl Chlorides with Aryl Grignard Reagents (Kumada Reaction) Mediated by a Palladium/Imidazolium Chloride System
inferredcites →https://doi.org/10.1021/jo025732jopenalex-snapshot
Air Stable, Sterically Hindered Ferrocenyl Dialkylphosphines for Palladium-Catalyzed C−C, C−N, and C−O Bond-Forming Cross-Couplings
inferredcites →https://doi.org/10.1021/jo035309qopenalex-snapshot
Preparation and Palladium-Catalyzed Cross-Coupling of Aryl Triethylammonium Bis(catechol) Silicates with Aryl Triflates
inferredcites →https://doi.org/10.1021/jo0505223openalex-snapshot
Novel and Efficient Access to Phenylamino-pyrimidine Type Protein Kinase C Inhibitors Utilizing a Negishi Cross-Coupling Strategy
inferredcites →https://doi.org/10.1021/jo051304copenalex-snapshot
Room-Temperature Negishi Cross-Coupling of Unactivated Alkyl Bromides with Alkyl Organozinc Reagents Utilizing a Pd/N-Heterocyclic Carbene Catalyst
inferredcites →https://doi.org/10.1021/jo0519615openalex-snapshot
Synthesis of the Benzhydryl Motif via a Suzuki−Miyaura Coupling of Arylboronic Acids and 3-Chloroacrylonitriles
inferredcites →https://doi.org/10.1021/jo052250+openalex-snapshot
Iron−Phosphine, −Phosphite, −Arsine, and −Carbene Catalysts for the Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents
inferredcites →https://doi.org/10.1021/jo0613939openalex-snapshot
Oligoindenopyrenes: A New Class of Polycyclic Aromatics
inferredcites →https://doi.org/10.1021/jo970822nopenalex-snapshot
Palladium-Catalyzed Methylation of Aryl and Vinyl Halides by Stabilized Methylaluminum and Methylgallium Complexes
inferredcites →https://doi.org/10.1021/ol0360288openalex-snapshot
Efficient Aqueous-Phase Heck and Suzuki Couplings of Aryl Bromides Using Tri(4,6-dimethyl-3- sulfonatophenyl)phosphine Trisodium Salt (TXPTS)
inferredcites →https://doi.org/10.1021/ol049779yopenalex-snapshot
Iron-Catalyzed Grignard Cross-Coupling with Alkyl Halides Possessing β-Hydrogens
inferredcites →https://doi.org/10.1021/ol0514909openalex-snapshot
The First Negishi Cross-Coupling Reaction of Two Alkyl Centers Utilizing a Pd−N-Heterocyclic Carbene (NHC) Catalyst
inferredcites →https://doi.org/10.1021/ol062339hopenalex-snapshot
1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols
inferredcites →https://doi.org/10.1021/ol0623769openalex-snapshot
Copper-Free Synthesis of Skipped Diynes via Cross-Coupling Reactions of Alkynylalanes with Propargylic Electrophiles
inferredcites →https://doi.org/10.1021/om00105a040openalex-snapshot
Synthesis and structure of the sterically crowded trimesitylaluminum-tetrahydrofuran adduct
inferredcites →https://doi.org/10.1021/om049106jopenalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions with Zinc, Boron, and Indium Exhibiting High Turnover Numbers (TONs): Use of Bidentate Phosphines and Other Critical Factors in Achieving High TONs†
inferredcites →https://doi.org/10.1039/b208609nopenalex-snapshot
Simple tricyclohexylphosphine–palladium complexes as efficient catalysts for the Stille coupling of deactivated aryl chlorides
inferredcites →https://doi.org/10.1055/s-2000-6373openalex-snapshot
Palladium-Catalyzed Cross-Methylation of Aryl Chlorides by Stabilized Dimethylaluminium and -Gallium Reagents

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.4651063openalex-extracted
Copper-Assisted Palladium Catalyzed the Cross-Coupling Reaction of Alknylalane Reagents with 2-Thiobenzo[D]Thiazoles Via C-S Bond Cleavage
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0835openalex-snapshot
The Preparation and Cross‐Coupling Reactions of Organoaluminum Compounds
inferred← citeshttps://doi.org/10.1002/9780470976548.ch3openalex-snapshot
Formal Oxidation State +3: Organometallic Chemistry
inferred← citeshttps://doi.org/10.1002/9783527655588.ch9openalex-snapshot
Cross‐Coupling Reactions to sp Carbon Atoms
inferred← citeshttps://doi.org/10.1002/adsc.200800169openalex-snapshot
A New Aspect of Magnesium Bromide‐Promoted Enantioselective Aryl Additions of Triaryl(tetrahydrofuran)aluminum to Ketones Catalyzed by a Titanium(IV) Catalyst of trans‐1,2‐Bis(hydroxycamphorsulfonylamino)cyclohexane
inferred← citeshttps://doi.org/10.1002/adsc.201000311openalex-snapshot
Extremely Efficient Cross‐Coupling of Benzylic Halides with Aryltitanium Tris(isopropoxide) Catalyzed by Low Loadings of a Simple Palladium(II) Acetate/Tris(p‐tolyl)phosphine System
inferred← citeshttps://doi.org/10.1002/adsc.201300075openalex-snapshot
A Highly Active and General Catalyst for the Stille Coupling Reaction of Unreactive Aryl, Heteroaryl, and Vinyl Chlorides under Mild Conditions
inferred← citeshttps://doi.org/10.1002/adsc.70757openalex-snapshot
Unlocking the Potential of Organoaluminum Reagents for Versatile C─C Couplings Using YPhos‐Pd Catalysts
inferred← citeshttps://doi.org/10.1002/ange.200904033openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Aryl Halides Using Organotitanium Nucleophiles
inferred← citeshttps://doi.org/10.1002/ange.201003813openalex-snapshot
Diastereoselektive Synthese von Homoallylalkoholen mit benachbarten tertiären und quartären Zentren mithilfe funktionalisierter allylischer Aluminiumreagentien
inferred← citeshttps://doi.org/10.1002/ange.201205987openalex-snapshot
Direkte Pd‐katalysierte Kreuzkupplung von funktionalisierten Organoaluminiumreagentien
inferred← citeshttps://doi.org/10.1002/ange.201412249openalex-snapshot
Organoaluminum‐Mediated Direct Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.200904033openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Aryl Halides Using Organotitanium Nucleophiles
inferred← citeshttps://doi.org/10.1002/anie.201003813openalex-snapshot
Diastereoselective Synthesis of Homoallylic Alcohols with Adjacent Tertiary and Quaternary Centers by Using Functionalized Allylic Aluminum Reagents
inferred← citeshttps://doi.org/10.1002/anie.201205987openalex-snapshot
Direct Pd‐Catalyzed Cross‐Coupling of Functionalized Organoaluminum Reagents
inferred← citeshttps://doi.org/10.1002/anie.201412249openalex-snapshot
Organoaluminum‐Mediated Direct Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chin.200806083openalex-snapshot
ChemInform Abstract: AlAr3(THF): Highly Efficient Reagents for Cross‐Couplings with Aryl Bromides and Chlorides Catalyzed by the Economic Palladium Complex of PCy3.
inferred← citeshttps://doi.org/10.1002/chir.20572openalex-snapshot
1,3‐bis[N‐sulfonyl‐(1R,2S)‐1,3‐diphenyl‐2‐aminopropanol]benzene: An excellent ligand for titanium‐catalyzed asymmetric AlPh3(THF) additions to aldehydes
inferred← citeshttps://doi.org/10.1002/chir.21018openalex-snapshot
Room temperature and highly enantioselective additions of alkyltitanium reagents to aldehydes catalyzed by a titanium catalyst of (R)‐h8‐binol
inferred← citeshttps://doi.org/10.1002/ejoc.201301757openalex-snapshot
Rhodium‐Catalyzed Cross‐Coupling of Vinylarenes with Arylaluminum Reagents in the Presence of Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.201402464openalex-snapshot
Synthesis of N , N ‐Disubstituted 3‐Amino‐1,4‐diynes and 3‐Amino‐1‐ynes by Addition of Alkynyldimethylaluminum Reagents to N , N ‐Disubstituted Formamides and N,O‐Acetals
inferred← citeshttps://doi.org/10.1002/ejoc.201403008openalex-snapshot
Highly Efficient Synthesis of Allenes from Trimethylaluminum Reagent and Propargyl Acetates Mediated by a Palladium Catalyst
inferred← citeshttps://doi.org/10.1007/3418_2012_39openalex-snapshot
Organoaluminum Couplings to Carbonyls, Imines, and Halides
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Palladium-catalyzed, ligand-free SN2’ substitution reactions of organoaluminum with propargyl acetates for the synthesis of multi-substituted allenes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.121040openalex-snapshot
Nickel-catalyzed cross-coupling of organoaluminum reagents with alkynylhalides for the synthesis of symmetrical and unsymmetrical conjugated 1,3-diynes derivatives
inferred← citeshttps://doi.org/10.1016/j.polymer.2008.01.055openalex-snapshot
Synthesis and application of polymer-supported N-sulfonylated aminoalcohols as enantioselective catalysts
inferred← citeshttps://doi.org/10.1016/j.tet.2009.04.057openalex-snapshot
The effect of ortho-substitution on the efficacy of biphenyls in mediating electron transfer from lithium
inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.072openalex-snapshot
Palladium-catalyzed coupling reactions of (ArCH2)Ti(O-i-Pr)3 with aromatic or heteroaromatic bromides
inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.004openalex-snapshot
Nickel-catalyzed cross-coupling of aryl or 2-menaphthyl quaternary ammonium triflates with organoaluminum reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2018.08.050openalex-snapshot
Highly efficient synthesis of 1,2-disubstituted acetylenes derivatives from the cross-coupling reactions of 1-bromoalkynes with organoalane reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132549openalex-snapshot
Simple and efficient nickel-catalyzed cross-coupling reaction of alkenylalanes with alkynyl halides for synthesis of conjugated enynes
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132564openalex-snapshot
Cross-coupling reaction of organoalane reagents with 2-mercaptobenzo-5-membered heterocycles for efficient synthesis of benzo-5-membered heterocycle sulfides
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133850openalex-snapshot
Copper-assisted palladium catalyzed the cross-coupling reaction of Alknylalane reagents with 2-Thiobenzo[d]thiazoles via C–S bond cleavage
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134089openalex-snapshot
Synthesis of the 2-alkynyl benzo[b]furanes/benzo[b]thiophenes from the cross-coupling reaction of benzo[b]furanyl/ benzo[b]thiophene aluminum reagents with gem-dibromoolefin derivatives catalyzed by palladium
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.05.018openalex-snapshot
Synthesis, characterization, and structures of arylaluminum reagents and asymmetric arylation of aldehydes catalyzed by a titanium complex of an N-sulfonylated amino alcohol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.091openalex-snapshot
Organoallylaluminum reagents promote easy access to trihalomethyl triazolyl homoallylic alcohols analogous to rufinamide
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02077openalex-snapshot
General Copper-Catalyzed Coupling of Alkyl-, Aryl-, and Alkynylaluminum Reagents with Organohalides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04175openalex-snapshot
A General and Selective Synthesis of Methylmonochlorosilanes from Di-, Tri-, and Tetrachlorosilanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02933openalex-snapshot
Transmetal-Catalyzed Enantioselective Cross-Coupling Reaction of Racemic Secondary Benzylic Bromides with Organoaluminum Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02923openalex-snapshot
Palladium-Catalyzed Carbonylative Coupling of Aryl Iodides with Alkenylaluminum Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04414openalex-snapshot
Palladium-Catalyzed Synthesis of 1,2-Diketones from Aryl Halides and Organoaluminum Reagents Using tert-Butyl Isocyanide as the CO Source
inferred← citeshttps://doi.org/10.1021/acscatal.2c04396openalex-snapshot
Regioselective Benzylic C–H Alumination and Further Functionalization of 2-Alkylpyridines by Yttrium Catalyst
inferred← citeshttps://doi.org/10.1021/acscatal.7b01058openalex-snapshot
Revisitation of Organoaluminum Reagents Affords a Versatile Protocol for C–X (X = N, O, F) Bond-Cleavage Cross-Coupling: A Systematic Study
inferred← citeshttps://doi.org/10.1021/jacs.1c10106openalex-snapshot
Missing Link in the Growth of Lead-Based Zintl Clusters: Isolation of the Dimeric Plumbaspherene [Cu4Pb22]4–
inferred← citeshttps://doi.org/10.1038/nchem.590openalex-snapshot
Preparation of functionalized organoaluminiums by direct insertion of aluminium to unsaturated halides
inferred← citeshttps://doi.org/10.1039/b802441copenalex-snapshot
Chiral tertiary 2-furyl alcohols: diversified key intermediates to bioactive compounds. Their enantioselective synthesis via (2-furyl)aluminium addition to ketones catalyzed by a titanium catalyst of (S)-BINOL
inferred← citeshttps://doi.org/10.1039/b917711fopenalex-snapshot
Room temperature Stille cross-coupling reaction of unreactive aryl chlorides and heteroaryl chlorides
inferred← citeshttps://doi.org/10.1039/c0cc01216eopenalex-snapshot
The first iron-catalysed aluminium-variant Negishi coupling: critical effect of co-existing salts on the dynamic equilibrium of arylaluminium species and their reactivity
inferred← citeshttps://doi.org/10.1039/c1cc14206bopenalex-snapshot
Simple and efficient nickel-catalyzed cross-coupling reaction of alkynylalanes with benzylic and aryl bromides
inferred← citeshttps://doi.org/10.1039/c2ob25303hopenalex-snapshot
An efficient nickel-catalyzed alkenylation of functionalized benzylic halides with alkenylaluminum reagents
inferred← citeshttps://doi.org/10.1039/c4ob00677aopenalex-snapshot
Nickel-catalyzed substitution reactions of propargyl halides with organotitanium reagents
inferred← citeshttps://doi.org/10.1039/c5qo00147aopenalex-snapshot
Regio- and stereoselective multisubstituted olefin synthesis via hydro/carboalumination of alkynes and subsequent iron-catalysed cross-coupling reaction with alkyl halides
inferred← citeshttps://doi.org/10.1039/c7ra02758copenalex-snapshot
Highly efficient synthesis of unsymmetrical 1,3-diynes from organoalane reagents and alkynyl bromides mediated by a nickel catalyst
inferred← citeshttps://doi.org/10.1039/c9qo01537jopenalex-snapshot
Palladium-catalyzed cross-coupling of (hetero)aryl or alkenyl sulfonates with aryl titanium as the multi-functional reagent
inferred← citeshttps://doi.org/10.1039/d3nj02026fopenalex-snapshot
The cross-coupling reaction of organoalane reagents with 2-methylthiobenzo[ d ]thiazoles via C–S bond cleavage catalyzed by nickel
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