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Palladium-Catalyzed Methylation of Aryl and Vinyl Halides by Stabilized Methylaluminum and Methylgallium Complexes
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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/anie.198307791openalex-snapshot
27AI‐NMR Spectroscopy: A Probe for Three‐, Four‐, Five‐, and Sixfold Coordinated Al Atoms in Organoaluminum Compounds
inferredcites →https://doi.org/10.1002/anie.198810771openalex-snapshot
Intramolecularly Stabilized Organogallium Compounds
inferredcites →https://doi.org/10.1002/cber.19580910637openalex-snapshot
Trimethylnaphthaline durch Chlormethylierung von Dimethylnaphthalinen
inferredcites →https://doi.org/10.1002/cber.19911240520openalex-snapshot
Intramolecular, Metallacyclic Organoaluminium, ‐gallium and ‐indium Addition Compounds Crystal Structure of 1‐Galla‐5‐azabicyclo[3.3.3]undecane
inferredcites →https://doi.org/10.1002/cber.19951280510openalex-snapshot
Syntheses and Structures of Intramolecularly Stabilized Organoaluminium Compounds
inferredcites →https://doi.org/10.1002/jlac.19043320104openalex-snapshot
Ueber symmetrische Biphenylderivate
inferredcites →https://doi.org/10.1002/jlac.19677050103openalex-snapshot
Metallorganische Verbindungen, XLV. Komplex‐Bildung und Reaktionen von Methylaluminium‐Verbindungen mit Diglyme
inferredcites →https://doi.org/10.1002/zaac.19804620116openalex-snapshot
Koordinationschemische Untersuchungen an Zinkdialkylen. XIV. Über Lithium‐ und Zink‐3‐(N, N‐dialkylamino)‐propyl‐Verbindungen
inferredcites →https://doi.org/10.1016/0022-0248(91)90475-kopenalex-snapshot
Physical properties of non-pyrophoric group III precursors for MOVPE
inferredcites →https://doi.org/10.1016/0022-328x(95)05917-eopenalex-snapshot
Intramolecularly stabilized organoaluminium and organogallium compounds: synthesis and X-ray crystal structures of some dimethylaluminium and -gallium alkoxides Me2MOROR′ and amides Me2MNHROR′
inferredcites →https://doi.org/10.1016/0022-4073(79)90030-xopenalex-snapshot
Comprehensive organic chemistry
inferredcites →https://doi.org/10.1016/s0022-328x(00)99320-3openalex-snapshot
Pentacoordinate [8-(dimethylamino)naphthyl]diorganotin halides containing a rigid, flat chelate ring. An unexpected redistribution reaction between [8-(dimethylamino)naphthyl]trimethyltin and trimethyltin halide
inferredcites →https://doi.org/10.1016/s0277-5387(00)80590-2openalex-snapshot
Novel intramolecularly stabilized organogallium and organoindium compounds and their use in MOVPE
inferredcites →https://doi.org/10.1021/ar00049a001openalex-snapshot
Recent Developments and New Perspectives in the Heck Reaction
inferredcites →https://doi.org/10.1021/cen-v060n019.p050openalex-snapshot
Comprehensive Organometallic Chemistry
inferredcites →https://doi.org/10.1021/ic50163a020openalex-snapshot
Chelation in organoaluminum-nitrogen chemistry
inferredcites →https://doi.org/10.1021/ja00400a074openalex-snapshot
Selective carbon-carbon bond formation via transition-metal catalysis. Part 18. Palladium-catalyzed stereo- and regiospecific coupling of allylic derivatives with alkenyl- and arylmetals. A highly selective synthesis and 1,4-dienes
inferredcites →https://doi.org/10.1021/ja00437a067openalex-snapshot
A novel stereospecific alkenyl-alkenyl cross-coupling by a palladium- or nickel-catalyzed reaction of alkenylalanes with alkenyl halides
inferredcites →https://doi.org/10.1021/ja00475a059openalex-snapshot
Selective carbon-carbon bond formation via transition metal catalysts. 9. Double metal catalysis in the cross-coupling reaction and its application to the stereo- and regioselective synthesis of trisubstituted olefins
inferredcites →https://doi.org/10.1021/ja01160a089openalex-snapshot
Alkenylbiphenyls. I. o-Substituted
inferredcites →https://doi.org/10.1021/ja01302a066openalex-snapshot
The Reaction of Potassium Amide in Liquid Ammonia with Diarylbromoethenes
inferredcites →https://doi.org/10.1021/jo00045a051openalex-snapshot
Convenient method for the synthesis of C-alkylated purine nucleosides: palladium-catalyzed cross-coupling reaction of halogenopurine nucleosides with trialkylaluminums
inferredcites →https://doi.org/10.1021/jo01362a041openalex-snapshot
Formation of Naphthalenes from Indenes. IV.1 The Effect of Substitution at the Ethylenic Double Bond*
inferredcites →https://doi.org/10.1021/om00055a057openalex-snapshot
Synthesis and characterization of alkylaluminum and -gallium derivatives of 2-(methylthio)- and 2-methoxyphenol. Crystal structures of the dimeric complexes [R2M(.mu.-OC6H4-2-ECH3)]2 (M = aluminum, E = S, R = Me, iso-Bu; M = Al, E = O, R = Et, iso-Bu; M = gallium, E = O, R = Me) featuring five…
inferredcites →https://doi.org/10.1039/jr9480001395openalex-snapshot
284. Syntheses of some asymmetric naphthalene and acenaphthene hydrocarbons
inferredcites →https://doi.org/10.1055/s-1996-4334openalex-snapshot
[(3-Dimethylamino)propyl]dimethylaluminum: A Convenient Reagent for Methylation and Ethynylation of Carbonyl Compounds
inferredcites →https://doi.org/10.1071/ch9890279openalex-snapshot
Palladium-Mediated Transformations of Heteroaromatic Triflates
inferredcites →https://doi.org/10.1139/v75-007openalex-snapshot
Synthesis and Crystal and Molecular Structures of the N,N-Dimethylethanol-aminogallane and N,N-Dimethylethanolaminogallium Dimethyl Dimers
inferredcites →https://doi.org/10.15227/orgsyn.062.0031openalex-snapshot
PALLADIUM-CATALYZED SYNTHESIS OF 1,4-DIENES BY ALLYLATION OF ALKENYLALANES:a-FARNESENE
inferredcites →https://doi.org/10.3891/acta.chem.scand.16-0155openalex-snapshot
On a New Type of Rearrangement during Ring-closure.
inferredcites →https://doi.org/10.3987/r-1984-10-2317openalex-snapshot
Introduction of the Methyl Group into the Pyrazine Ring
inferredcites →https://doi.org/10.3987/s(b)-1982-01-0117openalex-snapshot
A Regiospecific Synthesis of Carbosubstituted Heteroaromatic Derivatives via Pd-Catalyzed Cross Coupling
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/10.1002/1099-0690(200104)2001:8<1483::aid-ejoc1483>3.0.co;2-uopenalex-snapshot
Extending the Chemistry of [5.5.5.5]Fenestranes − Eightfold Peripheral Functionalization of Fenestrindanes
inferred← citeshttps://doi.org/10.1002/1099-0690(200205)2002:10<1628::aid-ejoc1628>3.0.co;2-copenalex-snapshot
Palladium-Catalyzed Cross-Methylation of Haloarenes Possessing Active Hydrogen Atoms by Intramolecularly Stabilized Dimethylindium and Dimethylaluminum Reagents
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.ch11openalex-snapshot
Group 13 Metal‐Mediated Organic Reactions
inferred← citeshttps://doi.org/10.1002/9780471264194.fos04307openalex-snapshot
(3‐Dimethylaminopropyl)dimethylgallium
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07712openalex-snapshot
Palladium(II) chloride–Phosphine
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07712.pub2openalex-snapshot
Palladium(II) chloride–Phosphine
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07712.pub3openalex-snapshot
Palladium(II) chloride–Phosphine
inferred← citeshttps://doi.org/10.1002/adsc.200505405openalex-snapshot
User‐Friendly Methylation of Aryl and Vinyl Halides and Pseudohalides with DABAL‐Me 3
inferred← citeshttps://doi.org/10.1002/adsc.201400984openalex-snapshot
Recent Advances in Transition Metal‐Catalyzed Methylation Reactions
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.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/ange.201706064openalex-snapshot
LiTMP Trans‐Metal‐Trapping of Fluorinated Aromatic Molecules: A Comparative Study of Aluminum and Gallium Carbanion Traps
inferred← citeshttps://doi.org/10.1002/ange.202508710openalex-snapshot
Rapid Methylation of Aryl Bromides Using Air‐Stable DABCO‐Bis(Trimethylaluminum) via Nickel Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202511648openalex-snapshot
Acetone Derivatives for Nickel‐Catalyzed Methylation, Trideuteromethylation, and 13C‐Methylation of (Hetero)Aryl Chlorides
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/anie.201706064openalex-snapshot
LiTMP Trans‐Metal‐Trapping of Fluorinated Aromatic Molecules: A Comparative Study of Aluminum and Gallium Carbanion Traps
inferred← citeshttps://doi.org/10.1002/anie.202508710openalex-snapshot
Rapid Methylation of Aryl Bromides Using Air‐Stable DABCO‐Bis(Trimethylaluminum) via Nickel Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202511648openalex-snapshot
Acetone Derivatives for Nickel‐Catalyzed Methylation, Trideuteromethylation, and 13 C‐Methylation of (Hetero)Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/chem.201801806openalex-snapshot
Dodecabromo‐ and Dodecaiodocentrohexaindane: Td‐Symmetrical Key Building Blocks for Twelve‐Fold Cross‐Coupling Reactions and Six‐Fold Orthogonal Extension
inferred← citeshttps://doi.org/10.1002/chin.199821062openalex-snapshot
ChemInform Abstract: Palladium‐Catalyzed Methylation of Aryl and Vinyl Halides by Stabilized Methylaluminum and Methylgallium Complexes.
inferred← citeshttps://doi.org/10.1002/ejic.200390179openalex-snapshot
Five‐ and Six‐Membered Cobaltocycles with C,P‐Chelating Ligands through Regiospecific Cyclometalation of Mono(2‐Substituted) Triphenylphosphane
inferred← citeshttps://doi.org/10.1002/ejoc.200900104openalex-snapshot
New and Efficient Iron Halide Mediated Synthesis of Alkenyl Halides through Coupling of Alkynes and Alcohols
inferred← citeshttps://doi.org/10.1002/jhet.5570400402openalex-snapshot
Palladium catalyzed cross‐methylation of bromoheterocycles with intramolecularly stabilized dimethyl indium reagents
inferred← citeshttps://doi.org/10.1002/zaac.200400033openalex-snapshot
Intramolekular stickstoffstabilisierte Organoaluminiumverbindungen mit Naphthyl‐, Benzyl‐ und Phenylliganden
inferred← citeshttps://doi.org/10.1002/zaac.200400236openalex-snapshot
1‐Aminoindan‐2‐ol, a Suitable Ligand for the Synthesis of Chiral, Intramolecularly Stabilized Compounds of Aluminum, Gallium, and Indium
inferred← citeshttps://doi.org/10.1002/zaac.200600033openalex-snapshot
Monoalkylaluminium Complexes Stabilized by a Rigid Dianionic Diimine Ligand: Synthesis, Solid State Structure, and Dynamic Solution Behaviour of (dpp‐BIAN)AlR (R = Me, Et, iBu)
inferred← citeshttps://doi.org/10.1002/zaac.200700154openalex-snapshot
Synthese und Charakterisierung neuer intramolekular phosphorstabilisierter Aluminium‐, Gallium‐ und Indiumorganyle
inferred← citeshttps://doi.org/10.1002/zaac.200700411openalex-snapshot
C‐O Bond Cleavage of Diethyl Ether and Tetrahydrofurane by [(dpp‐BIAN)AlI(Et2O)] [dpp‐BIAN = 1,2‐bis[(2,6‐di‐iso‐propylphenyl)‐imino]acenaphthene]
inferred← citeshttps://doi.org/10.1002/zaac.201300272openalex-snapshot
Peri‐Interactions in 8‐Diphenylphosphino‐1‐bromonaphthalene, 6‐Diphenylphosphino‐5‐bromoacenaphthene, and Derivatives
inferred← citeshttps://doi.org/10.1007/3418_2012_39openalex-snapshot
Organoaluminum Couplings to Carbonyls, Imines, and Halides
inferred← citeshttps://doi.org/10.1007/978-3-319-18690-0_5openalex-snapshot
Gold: Oxidative Addition to Au(I)
inferred← citeshttps://doi.org/10.1007/s42250-020-00172-1openalex-snapshot
C-Methylation of Organic Substrates: A Comprehensive Overview. Part II—Methyl Metals as Methylating Agents
inferred← citeshttps://doi.org/10.1016/b0-08-043748-6/09089-7openalex-snapshot
Metal Complexes as Catalysts for CC Cross-coupling Reactions
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00004-0openalex-snapshot
One or More CC Bond(s) Formed by Substitution: Substitution of Halogen
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00011-8openalex-snapshot
One or More CC Bond(s) Formed by Substitution or Addition
inferred← citeshttps://doi.org/10.1016/b978-0-323-99492-7.00005-6openalex-snapshot
Miscellaneous use of Raney nickel for the synthesis of heterocycles
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00064-3openalex-snapshot
One or More CC Bond(s) Formed by Substitution: Substitution of Halogen
inferred← citeshttps://doi.org/10.1016/j.apcata.2010.04.005openalex-snapshot
Palladium-catalysed methylation of aryl halides in ionic liquids with stabilized AlMe3
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.05.028openalex-snapshot
Gallium(III) and indium(III) alkoxides and aryloxides
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.12.023openalex-snapshot
Synthesis, biological evaluation and molecular modeling of a novel series of 7-azaindole based tri-heterocyclic compounds as potent CDK2/Cyclin E inhibitors
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Nickel-catalyzed cross-coupling of aryl or 2-menaphthyl quaternary ammonium triflates with organoaluminum reagents
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.tetlet.2005.12.133openalex-snapshot
α-Ethynylation reaction of ketones using catalytic amounts of trialkylgallium base
inferred← citeshttps://doi.org/10.1016/s0020-1693(02)00743-0openalex-snapshot
2,2′-Bipyridine, 2-(2-oxazolyl)pyridine and 2,2′-bisoxazole derived nickel(0) complexes as selective catalysts for cross-coupling of aryl chlorides by intramolecularly stabilized dialkylaluminum reagents
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)00767-1openalex-snapshot
Synthese und Charakterisierung chiraler Organogallium- und -aluminiumalkoholate mit intramolekularer Stickstoffstabilisierung. Röntgenstrukturanalyse von Dimethylgallium-(S)-2-dimethylamino-3-methyl-1-butanolat, Dimethylgallium-(S)-2-dimethylamino-3-phenyl-1-propanolat und…
inferred← citeshttps://doi.org/10.1016/s0022-328x(01)00738-0openalex-snapshot
Monomeric Group 13 compounds with bidentate (N,O) ligands
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00246-0openalex-snapshot
Multiply bridgehead- and periphery-substituted tribenzotriquinacenes—highly versatile rigid molecular building blocks with C3v or C3 symmetry
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01038-8openalex-snapshot
Practical methylation of aryl halides by Suzuki–Miyaura coupling
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01295-8openalex-snapshot
Dichlorobis(triphenylphosphine)nickel-catalyzed cross-coupling of aryl chlorides with intramolecularly stabilized group 13 metal alkylating reagents
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01054-5openalex-snapshot
Kinetic resolution of racemic 2,2′-bis(trifluoromethane-sulfonyloxy)-1,1′-binaphthalene by chiral dimethylaluminum complexes and an achiral Pd catalyst, as well as by achiral dimethylaluminum reagents in the presence of a chiral Pd catalyst
inferred← citeshttps://doi.org/10.1016/s1381-1169(00)00442-8openalex-snapshot
Palladium-catalyzed cross-methylation of aryl triflates by intramolecularly stabilized dialkyl-aluminum, -gallium and -indium reagents
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00767openalex-snapshot
Copper-Catalyzed Electrophilic Amination of Organoaluminum Nucleophiles with O-Benzoyl Hydroxylamines
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.joc.5c01924openalex-snapshot
Copper Catalyzed the Cross-Coupling Reaction of Arylthioaluminum Reagents with Alkynyl Bromides/Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00304openalex-snapshot
Enantioselective Suzuki–Miyaura Chemistry: Route Evolution for the Synthesis of PKMYT1 Inhibitor XL495
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00027openalex-snapshot
Synthesis of 1,1′-Diarylethanes and Related Systems by Displacement of Trichloroacetimidates with Trimethylaluminum
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.5b02472openalex-snapshot
Fe-Promoted Chlorobenzylation of Terminal Alkynes through Benzylic C(sp3)–H Bond Functionalization
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/jo020169qopenalex-snapshot
Palladium-Catalyzed Cross-Alkynylation of Aryl Bromides by Sodium Tetraalkynylaluminates
inferred← citeshttps://doi.org/10.1021/jo061346gopenalex-snapshot
A Mild Synthesis of Vinyl Halides and gem -Dihalides Using Triphenyl Phosphite−Halogen-Based Reagents
inferred← citeshttps://doi.org/10.1021/jo4024123openalex-snapshot
Synthesis of Heteroaryl Compounds through Cross-Coupling Reaction of Aryl Bromides or Benzyl Halides with Thienyl and Pyridyl Aluminum Reagents
inferred← citeshttps://doi.org/10.1021/jo502839eopenalex-snapshot
β-Selective C-Arylation of Silyl Protected 1,6-Anhydroglucose with Arylalanes: The Synthesis of SGLT2 Inhibitors
inferred← citeshttps://doi.org/10.1021/ol061231zopenalex-snapshot
Regioselective Pd-Catalyzed Synthesis and Application of 3-Methyl-5-bromo-2-pyrone toward Keto-phomactin A
inferred← citeshttps://doi.org/10.1021/ol401952kopenalex-snapshot
Lewis Base Directed Cycloaddition Reactions of 2-Pyrones and Alkynylaluminum Reagents
inferred← citeshttps://doi.org/10.1021/om0491037openalex-snapshot
Monomeric Alkylaluminum Complexes (dpp-BIAN)AlR2 (R = Me, Et, iBu) Supported by the Rigid Chelating Radical-Anionic 1,2-Bis[(2,6-diisopropylphenyl)imino]acenaphthene Ligand (dpp-BIAN)
inferred← citeshttps://doi.org/10.1021/om200854nopenalex-snapshot
Selective Dialkylation of a Doubly Linked Dicyclopentadiene Ligand and the Ensuing Ruthenium Complexes
inferred← citeshttps://doi.org/10.1021/om3009469openalex-snapshot
Co-complexation Syntheses, Structural Characterization, and DFT Studies of a Novel Series of Polymeric Alkali-Metal Tetraorganogallates
inferred← citeshttps://doi.org/10.1021/om900460uopenalex-snapshot
Synthesis, Structures, and Characterizations of [ArTi(O-i-Pr)3]2and Efficient Room-Temperature Aryl−Aryl Coupling of Aryl Bromides with [ArTi(O-i-Pr)3]2Catalyzed by the Economic Pd(OAc)2/PCy3System
inferred← citeshttps://doi.org/10.1038/nchem.2587openalex-snapshot
New ligands for nickel catalysis from diverse pharmaceutical heterocycle libraries
inferred← citeshttps://doi.org/10.1038/s41467-026-69467-0openalex-snapshot
Formaldehyde hydrazone as a methyl reagent for nickel-catalyzed cross-coupling methylation of aryl and heteroaryl electrophiles
inferred← citeshttps://doi.org/10.1039/a802867bopenalex-snapshot
Main group organometallics in organic synthesis
inferred← citeshttps://doi.org/10.1039/b707703copenalex-snapshot
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/10.1039/b718998bopenalex-snapshot
Methylation of arenes via Ni-catalyzed aryl C–O/F activation
inferred← citeshttps://doi.org/10.1039/c4ob01594kopenalex-snapshot
Direct C–H bond arylation of fluorenes with aryl chlorides catalyzed by N-heterocyclic carbene–palladium( ii )–1-methylimidazole complex and further transformation of the products in a one-pot procedure
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/d0ra02984jopenalex-snapshot
Palladium-catalyzed cross-coupling reaction of alkenyl aluminums with 2-bromobenzo[ b ]furans
inferred← citeshttps://doi.org/10.1039/d2sc03294eopenalex-snapshot
Palladium-catalyzed nucleomethylation of alkynes for synthesis of methylated heteroaromatic compounds
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
inferred← citeshttps://doi.org/10.1039/d4cc02112fopenalex-snapshot
Facile methyl group transfer from Pt II to gallium and indium
inferred← citeshttps://doi.org/10.1055/s-0036-1589107openalex-snapshot
Sixfold Peripheral Halogenation of Tribenzotriquinacenes: An Alternative Access to Useful TBTQ Building Blocks
inferred← citeshttps://doi.org/10.1080/00397911.2010.526282openalex-snapshot
Synthesis of 2-(3′Bromo-3′-phenylallyl)indoles via ZnBr2-Mediated Addition of Bromomethylindoles/Indolylmethylacetates with Phenylacetylene
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-4bc19openalex-snapshot
Nickel-Catalyzed Cross-Coupling Methylation of Aryl and Heteroaryl Electrophiles via Hydrazone Umpolung
inferred← citeshttps://doi.org/10.3184/030823407x208319openalex-snapshot
Synthesis and Characterisation of Dialkyl[2-(2-phenolato)Oxazolines] of Gallium(III) and Indium(III): Crystal Structure of [{InMe 2 (OC 6 H 4 -OxMe 2 )} 2 ]
inferred← citeshttps://doi.org/10.3762/bjoc.11.261openalex-snapshot
Copper-catalyzed arylation of alkyl halides with arylaluminum reagents
inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.11.3382openalex-snapshot
Total Synthesis of (±)-Aspidospermidine Starting from 3-Ethyl-5-bromo-2-pyrone
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