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Cross-coupling of organosilanes with organic halides mediated by a palladium catalyst and tris(diethylamino)sulfonium difluorotrimethylsilicate

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inferred← citeshttps://doi.org/10.2139/ssrn.4847584openalex-extracted
Aryl/Hetero-Aryl Tosylates as Coupling Partners in Metal Mediated Suzuki and Hiyama Cross-Coupling Reactions in Ionic Liquids: Facile Synthesis of Biaryls/Heterobiaryls
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Potassium Organotrifluoroborates: New Partners in Palladium-Catalysed Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199911)1999:11<2957::aid-ejoc2957>3.0.co;2-7openalex-snapshot
Stereoselective Synthesis of (E)- and (Z)-Acetals of Pent-2-en-4-yn-1-al and Related Dienynes and Dienediynes
inferred← citeshttps://doi.org/10.1002/047084289x.ra045openalex-snapshot
Allyl Bromide
inferred← citeshttps://doi.org/10.1002/047084289x.rb098sopenalex-snapshot
Bis(allyl)di-μ-chlorodipalladium
inferred← citeshttps://doi.org/10.1002/047084289x.rb098s.pub2openalex-snapshot
Bis(allyl)di-μ-chlorodipalladium
inferred← citeshttps://doi.org/10.1002/047084289x.rn00785openalex-snapshot
2,4,6,8-Tetraethenyl-2,4,6,8-tetramethylcyclotetrasiloxane
inferred← citeshttps://doi.org/10.1002/047084289x.rn01732openalex-snapshot
1-Iodocyclohexene
inferred← citeshttps://doi.org/10.1002/047084289x.rt293openalex-snapshot
(E)-1-Trimethylsilyl-1,3-butadiene
inferred← citeshttps://doi.org/10.1002/047084289x.rt401openalex-snapshot
Tris(dimethylamino)sulfonium Difluorotrimethylsilicate
inferred← citeshttps://doi.org/10.1002/047084289x.rt401.pub2openalex-snapshot
Tris(dimethylamino)sulfonium Difluorotrimethylsilicate
inferred← citeshttps://doi.org/10.1002/0470862106.ia281openalex-snapshot
Organic Synthesis Using Metal‐Mediated Coupling Reactions
inferred← citeshttps://doi.org/10.1002/0471264180.or037.02openalex-snapshot
The Electrophilic Substitution of Allylsilanes and Vinylsilanes
inferred← citeshttps://doi.org/10.1002/0471264180.or075.03openalex-snapshot
Cross‐Coupling with Organosilicon Compounds
inferred← citeshttps://doi.org/10.1002/0471264180.or106.01openalex-snapshot
Alkene Cross‐Metathesis Reactions
inferred← citeshttps://doi.org/10.1002/0471264229.os083.07openalex-snapshot
S uzuki‐ M iyaura Cross‐Coupling: Preparation of 2′‐Vinylacetanilide
inferred← citeshttps://doi.org/10.1002/0471264229.os086.26openalex-snapshot
Vinylation with Inexpensive Silicon‐Based Reagents: Preparation of 3‐Vinylquinoline and 4‐Vinylbenzophenone
inferred← citeshttps://doi.org/10.1002/1099-0690(200112)2001:23<4391::aid-ejoc4391>3.0.co;2-dopenalex-snapshot
Pd/Ag-Catalyzed Direct Coupling of 1-Trimethylsilyl Alkynes with Vinyl Triflates
inferred← citeshttps://doi.org/10.1002/1521-3765(20010401)7:7<1455::aid-chem1455>3.0.co;2-uopenalex-snapshot
Imide-Amide Rearrangement of Cyclic Phosphorimidates: A Mechanistic Study
inferred← citeshttps://doi.org/10.1002/1521-3765(20020402)8:7<1637::aid-chem1637>3.0.co;2-7openalex-snapshot
Synthesis and Reactivity of anα-Stannylβ-Silyl Enamide
inferred← citeshttps://doi.org/10.1002/9780470126004.ch14openalex-snapshot
Preparation of Alkenes
inferred← citeshttps://doi.org/10.1002/9780470638859.conrr319openalex-snapshot
Hiyama Coupling
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0022openalex-snapshot
Reactions of Organic Halides Mediated by Transition Metal Compounds
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0192openalex-snapshot
Synthetic Applications of Allylsilanes and Vinylsilanes
inferred← citeshttps://doi.org/10.1002/9781118484722.ch3openalex-snapshot
Organosilicon and Relating Organotin Chemistry
inferred← citeshttps://doi.org/10.1002/9781118484722.ch5openalex-snapshot
Organopalladium Chemistry
inferred← citeshttps://doi.org/10.1002/9781118662083.cot02-007openalex-snapshot
Formation of Dienes and Polyenes
inferred← citeshttps://doi.org/10.1002/9781118662083.cot03-004openalex-snapshot
Alkylation, Alkenylation, and Arylation of Alkynes and Allenes
inferred← citeshttps://doi.org/10.1002/9781118681299.ch5openalex-snapshot
Transition Metal‐Mediated Carbon–Carbon Bond Forming Reactions
inferred← citeshttps://doi.org/10.1002/9781118750407.ch5openalex-snapshot
Palladium in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/9781119181286.ch5openalex-snapshot
Development of Homogeneous Catalysis and Organocatalysis
inferred← citeshttps://doi.org/10.1002/9781119942863.ch2openalex-snapshot
Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0263openalex-snapshot
Organic Synthesis Using Metal‐Mediated Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527612222.ch10openalex-snapshot
Organosilicon Compounds in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527619535.ch4openalex-snapshot
Organosilicon Compounds in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527619535.ch6openalex-snapshot
Cross‐Coupling Reactions to sp Carbon Atoms
inferred← citeshttps://doi.org/10.1002/9783527633678.ch5openalex-snapshot
Silicon‐Based Carbon–Carbon Bond Formation by Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1002/9783527635993.ch9openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527648283.ch12openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling Reactions – Industrial Applications
inferred← citeshttps://doi.org/10.1002/9783527651733.ch6openalex-snapshot
Cross Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527655588.ch7openalex-snapshot
Organosilicon Compounds in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527655588.ch9openalex-snapshot
Cross‐Coupling Reactions to sp Carbon Atoms
inferred← citeshttps://doi.org/10.1002/9783527664801.ch16openalex-snapshot
Case Study of Mechanisms in Synthetic Reactions
inferred← citeshttps://doi.org/10.1002/9783527671229.ch05openalex-snapshot
NHC Platinum(0) Complexes: Unique Catalysts for the Hydrosilylation of Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1002/9783527671403.hlc039openalex-snapshot
Designing Principles and Synthesis of Materials for Nematic Liquid Crystals
inferred← citeshttps://doi.org/10.1002/9783527672707.ch1openalex-snapshot
Cross‐Coupling Arylations: Precedents and Rapid HistoricalReview of the Field
inferred← citeshttps://doi.org/10.1002/9783527675142.ch18openalex-snapshot
Si–C – X and Si–C – EWG as Carbanion Equivalents under Lewis Base Activation ( n ?→?σ*)
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz08074openalex-snapshot
Hiyama cross‐coupling
inferred← citeshttps://doi.org/10.1002/9783527814787.ch8openalex-snapshot
Silyl‐ H eck, Silyl‐ N egishi, and Related Reactions
inferred← citeshttps://doi.org/10.1002/9783527814787.ch9openalex-snapshot
Transition‐Metal‐Catalyzed Cross‐coupling of Organosilicon Compounds
inferred← citeshttps://doi.org/10.1002/9783527828166.ch6openalex-snapshot
Pd ‐Catalyzed C C Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0170openalex-snapshot
Recent Developments on Transition Metal‐Free CC Cross‐Coupling Reactions Using Recyclable Catalysts
inferred← citeshttps://doi.org/10.1002/adsc.200303067openalex-snapshot
C(sp2)‐C(sp) and C(sp)‐C(sp) Coupling Reactions Catalyzed by Oxime‐Derived Palladacycles
inferred← citeshttps://doi.org/10.1002/adsc.200404188openalex-snapshot
Cross‐Coupling of Triallyl(aryl)silanes with Aryl Bromides and Chlorides: An Alternative Convenient Biaryl Synthesis
inferred← citeshttps://doi.org/10.1002/adsc.200404196openalex-snapshot
First Microwave‐Accelerated Hiyama Coupling of Aryl‐ and Vinylsiloxane Derivatives: Clean Cross‐Coupling of Aryl Chlorides within Minutes
inferred← citeshttps://doi.org/10.1002/adsc.200404309openalex-snapshot
Researchers in This Field Still Have Many Challenges in Front of Them, but the Future is Indeed Very Bright
inferred← citeshttps://doi.org/10.1002/adsc.200600262openalex-snapshot
The First Fluoride‐Free Hiyama Reaction of Vinylsiloxanes Promoted by Sodium Hydroxide in Water
inferred← citeshttps://doi.org/10.1002/adsc.200800118openalex-snapshot
An Electron‐Deficient Diene as Ligand for Palladium‐Catalyzed Cross‐Coupling Reactions: An Efficient Alkylation of Aryl Iodides by Primary and Secondary Alkylzinc Reagents
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.201000975openalex-snapshot
The Pyridyldiisopropylsilyl Group: A Masked Functionality and Directing Group for Monoselective ortho‐Acyloxylation and ortho‐Halogenation Reactions of Arenes
inferred← citeshttps://doi.org/10.1002/adsc.201300827openalex-snapshot
Iron‐Catalysed Chemo‐, Regio‐, and Stereoselective Hydrosilylation of Alkenes and Alkynes using a Bench‐Stable Iron(II) Pre‐Catalyst
inferred← citeshttps://doi.org/10.1002/adsc.201400178openalex-snapshot
Synthesis of Biaryls through Aromatic CH Bond Activation: A Review of Recent Developments
inferred← citeshttps://doi.org/10.1002/adsc.201500803openalex-snapshot
Regioselective Copper‐Catalyzed Oxidative Cross‐Coupling of Imidazo[1,2‐ a ]pyridines with Methyl Ketones: An Efficient Route for Synthesis of 1,2‐Diketones
inferred← citeshttps://doi.org/10.1002/adsc.201800099openalex-snapshot
A Palladium NNC‐Pincer Complex as an Efficient Catalyst Precursor for the Mizoroki−Heck Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201800343openalex-snapshot
Development of the Applications of Palladium on Charcoal in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/adsc.201801331openalex-snapshot
Recent Advances on Diverse Decarboxylative Reactions of Amino Acids
inferred← citeshttps://doi.org/10.1002/adsc.202200237openalex-snapshot
Strategic Applications of the β‐Silicon Effect
inferred← citeshttps://doi.org/10.1002/adsc.202301146openalex-snapshot
Synthesis of Styrenes and E‐Stilbenes by Palladium‐Catalyzed Vinylation of Aryl Iodides with 1,2‐Dibromoethane
inferred← citeshttps://doi.org/10.1002/adsc.202400707openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryl Alkyl Selenides with Aryl Bromides: Cross‐Coupling Between Two Electrophiles
inferred← citeshttps://doi.org/10.1002/ajoc.201600472openalex-snapshot
Highly Chemoselective DMPU‐Mediated Trialkylsilylation of Terminal Alkynes Using Trifluoromethyltrialkylsilane
inferred← citeshttps://doi.org/10.1002/ajoc.201900297openalex-snapshot
Palladium‐Catalysed Cross‐Coupling Reactions for the Synthesis of Chalcones
inferred← citeshttps://doi.org/10.1002/ajoc.202100792openalex-snapshot
Copper‐Catalyzed N‐Arylation of Indoles and Anilines with Aryltrialkoxysilanes
inferred← citeshttps://doi.org/10.1002/ajoc.202200179openalex-snapshot
Recent Advances in Microwave‐assisted Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ange.19931050309openalex-snapshot
Regiospezifische Synthese von 3,4‐disubstituierten Furanen aus 3,4‐Bis(trimethylsilyl)furan: eine neue Kupplungsreaktion mit Boroxinen vom Typ der Suzuki‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.19941062307openalex-snapshot
Kleider machen Leute: Heck‐Reaktion im neuen Gewand
inferred← citeshttps://doi.org/10.1002/ange.200463007openalex-snapshot
Organoschwefelverbindungen: elektrophile Reagentien für übergangsmetallkatalysierte C‐C‐Verknüpfungen
inferred← citeshttps://doi.org/10.1002/ange.200901884openalex-snapshot
Palladium‐Catalyzed Direct Arylation of Cyclic Enamides with Aryl Silanes by sp2 CH Activation
inferred← citeshttps://doi.org/10.1002/ange.200902471openalex-snapshot
Acid‐Catalyzed Intramolecular [2+2] Cycloaddition of Ene‐allenones: Facile Access to Bicyclo[n.2.0] Frameworks
inferred← citeshttps://doi.org/10.1002/ange.200905223openalex-snapshot
Stereoisomerically Pure Trisubstituted Vinylaluminum Reagents and their Utility in Copper‐Catalyzed Enantioselective Synthesis of 1,4‐Dienes Containing Z or E Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201006374openalex-snapshot
Vom Edelmetall zum Nobelpreis: Palladiumkatalysierte Kupplungen als Schlüsselmethode in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.201107017openalex-snapshot
Palladiumkatalysierte Kreuzkupplungen: eine historische Perspektive im Kontext der Nobel‐Preise 2010
inferred← citeshttps://doi.org/10.1002/ange.201608230openalex-snapshot
Tamejiro Hiyama
inferred← citeshttps://doi.org/10.1002/ange.201608667openalex-snapshot
Aryl(triethyl)silanes for Biaryl and Teraryl Synthesis by Copper(II)‐Catalyzed Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/ange.201702311openalex-snapshot
Synthesis of Aromatic Sulfones from SO2 and Organosilanes Under Metal‐free Conditions
inferred← citeshttps://doi.org/10.1002/ange.201708449openalex-snapshot
Experimental and Computational Exploration of para‐Selective Silylation with a Hydrogen‐Bonded Template
inferred← citeshttps://doi.org/10.1002/ange.201710866openalex-snapshot
Fluorinated Vinylsilanes from the Copper‐Catalyzed Defluorosilylation of Fluoroalkene Feedstocks
inferred← citeshttps://doi.org/10.1002/ange.201910169openalex-snapshot
Geometric E→Z Isomerisation of Alkenyl Silanes by Selective Energy Transfer Catalysis: Stereodivergent Synthesis of Triarylethylenes via a Formal anti‐Metallometallation
inferred← citeshttps://doi.org/10.1002/ange.202310851openalex-snapshot
Catalytic ipso‐Nitration of Organosilanes Enabled by Electrophilic N‐Nitrosaccharin Reagent
inferred← citeshttps://doi.org/10.1002/ange.202425256openalex-snapshot
Regio‐ and Enantioconvergent Hydroallylation of Acrylates Enabled by γ‐Silyl‐Substituted Allyl Acetates
inferred← citeshttps://doi.org/10.1002/ange.202508697openalex-snapshot
Electrochemical Deoxygenative Silylation of Alcohols
inferred← citeshttps://doi.org/10.1002/ange.202510069openalex-snapshot
Deoxygenative Functionalization of Alcohols and Carbonyl Compounds via Electrochemical Reduction
inferred← citeshttps://doi.org/10.1002/anie.199304321openalex-snapshot
Regiospecific Conversion of 3,4‐Bis(trimethylsilyl)furan to 3,4‐Disubstituted Furans: A Novel Suzuki‐Type Cross‐Coupling of Boroxines
inferred← citeshttps://doi.org/10.1002/anie.199423791openalex-snapshot
Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb
inferred← citeshttps://doi.org/10.1002/anie.200463007openalex-snapshot
Organosulfur Compounds: Electrophilic Reagents in Transition‐Metal‐Catalyzed Carbon–Carbon Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/anie.200901884openalex-snapshot
Palladium‐Catalyzed Direct Arylation of Cyclic Enamides with Aryl Silanes by sp2 CH Activation
inferred← citeshttps://doi.org/10.1002/anie.200902471openalex-snapshot
Acid‐Catalyzed Intramolecular [2+2] Cycloaddition of Ene‐allenones: Facile Access to Bicyclo[n.2.0] Frameworks
inferred← citeshttps://doi.org/10.1002/anie.200905223openalex-snapshot
Stereoisomerically Pure Trisubstituted Vinylaluminum Reagents and their Utility in Copper‐Catalyzed Enantioselective Synthesis of 1,4‐Dienes Containing Z or E Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201006374openalex-snapshot
From Noble Metal to Nobel Prize: Palladium‐Catalyzed Coupling Reactions as Key Methods in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201107017openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize
inferred← citeshttps://doi.org/10.1002/anie.201608230openalex-snapshot
Tamejiro Hiyama
inferred← citeshttps://doi.org/10.1002/anie.201608667openalex-snapshot
Aryl(triethyl)silanes for Biaryl and Teraryl Synthesis by Copper(II)‐Catalyzed Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/anie.201702311openalex-snapshot
Synthesis of Aromatic Sulfones from SO2 and Organosilanes Under Metal‐free Conditions
inferred← citeshttps://doi.org/10.1002/anie.201708449openalex-snapshot
Experimental and Computational Exploration of para‐Selective Silylation with a Hydrogen‐Bonded Template
inferred← citeshttps://doi.org/10.1002/anie.201710866openalex-snapshot
Fluorinated Vinylsilanes from the Copper‐Catalyzed Defluorosilylation of Fluoroalkene Feedstocks
inferred← citeshttps://doi.org/10.1002/anie.201910169openalex-snapshot
Geometric E→Z Isomerisation of Alkenyl Silanes by Selective Energy Transfer Catalysis: Stereodivergent Synthesis of Triarylethylenes via a Formal anti‐Metallometallation
inferred← citeshttps://doi.org/10.1002/anie.202310851openalex-snapshot
Catalytic ipso‐Nitration of Organosilanes Enabled by Electrophilic N‐Nitrosaccharin Reagent
inferred← citeshttps://doi.org/10.1002/anie.202425256openalex-snapshot
Regio‐ and Enantioconvergent Hydroallylation of Acrylates Enabled by γ‐Silyl‐Substituted Allyl Acetates
inferred← citeshttps://doi.org/10.1002/anie.202508697openalex-snapshot
Electrochemical Deoxygenative Silylation of Alcohols
inferred← citeshttps://doi.org/10.1002/aoc.1863openalex-snapshot
Application of a dimeric ortho‐palladated complex of tribenzylamine as an efficient catalyst in microwave‐assisted Hiyama coupling reactions
inferred← citeshttps://doi.org/10.1002/aoc.2921openalex-snapshot
Mechanistic study of palladium‐catalyzed decarboxylative coupling of phenylpropiolic acid and aryl iodide
inferred← citeshttps://doi.org/10.1002/aoc.3246openalex-snapshot
Pd(II) salen complex covalently anchored to multi‐walled carbon nanotubes as a heterogeneous and reusable precatalyst for Mizoroki–Heck and Hiyama cross‐coupling reactions
inferred← citeshttps://doi.org/10.1002/aoc.3494openalex-snapshot
Application of Pd‐2A3HP‐MCM‐41 to the Suzuki, Heck and Stille coupling reactions and synthesis of 5‐substituted 1H‐tetrazoles
inferred← citeshttps://doi.org/10.1002/aoc.3543openalex-snapshot
Piperazine‐ and DABCO‐bridged dinuclear N‐heterocyclic carbene palladium complexes: synthesis, structure and application to Hiyama coupling reaction
inferred← citeshttps://doi.org/10.1002/aoc.5140openalex-snapshot
Desulfinative palladium‐catalyzed cross‐coupling of arylsulfonyl hydrazides with aryl bromides under air
inferred← citeshttps://doi.org/10.1002/aoc.70617openalex-snapshot
Exclusive Hiyama‐Type C‐Si Arylation of Unactivated (E)‐β‐Trimethylsilyl Styrenes Catalyzed by Pd Nanoparticles in 1,3‐Dimethyl‐2‐Imidazolidinone (DMI)
inferred← citeshttps://doi.org/10.1002/asia.200900503openalex-snapshot
Efficient Preparation of Photoswitchable Dithienylethene‐Linker‐Conjugates by Palladium‐Catalyzed Coupling Reactions of Terminal Alkynes with Thienyl Chlorides and Other Aryl Halides
inferred← citeshttps://doi.org/10.1002/asia.201301371openalex-snapshot
Amine‐Catalyzed Direct Photoarylation of Unactivated Arenes
inferred← citeshttps://doi.org/10.1002/bkcs.11013openalex-snapshot
Magnetic Pd– Fe3O4 Heterodimer Nanocrystals as Recoverable Catalysts for Ligand‐Free Hiyama Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/bkcs.70204openalex-snapshot
A brief historical overview of organometallic chemistry in organic synthesis: From the 19th to the 20th century
inferred← citeshttps://doi.org/10.1002/cbic.200500290openalex-snapshot
Regioselective Carbon–Carbon Bond Formation in Proteins with Palladium Catalysis; New Protein Chemistry by Organometallic Chemistry
inferred← citeshttps://doi.org/10.1002/cctc.201100320openalex-snapshot
The Direct Arylation of Unactivated Arenes with Aryl Halides Catalyzed by a Magnetically Recyclable Fe‐Ni Alloy
inferred← citeshttps://doi.org/10.1002/cctc.201403057openalex-snapshot
Recent Applications of Magnetically Recoverable Nanocatalysts in CC and CX Coupling Reactions
inferred← citeshttps://doi.org/10.1002/cctc.201500068openalex-snapshot
Synthesis of Biaryls by Decarboxylative Hiyama Coupling
inferred← citeshttps://doi.org/10.1002/cctc.201800159openalex-snapshot
From Remote Alkenes to Linear Silanes or Allylsilanes depending on the Metal Center
inferred← citeshttps://doi.org/10.1002/cctc.201800161openalex-snapshot
Solution Synthesis of N,N‐Dimethylformamide‐Stabilized Iron‐Oxide Nanoparticles as an Efficient and Recyclable Catalyst for Alkene Hydrosilylation
inferred← citeshttps://doi.org/10.1002/cctc.202401190openalex-snapshot
A Highly Efficient Cross‐Coupling Mode via the Release of Small Molecules: Transition Metal‐Catalyzed Unimolecular Fragment Coupling (UFC)
inferred← citeshttps://doi.org/10.1002/cctc.202402136openalex-snapshot
A Comprehensive Review of Intramolecular Hydrosilylation of Alkynes and Alkenes
inferred← citeshttps://doi.org/10.1002/cctc.202500121openalex-snapshot
Catalytic Silylation of Alkynyl C(sp)–H Bonds with tert ‐Butyl‐Substituted Silyldiazenes
inferred← citeshttps://doi.org/10.1002/chem.200600206openalex-snapshot
A User‐Friendly, All‐Purpose Pd–NHC (NHC=N‐Heterocyclic Carbene) Precatalyst for the Negishi Reaction: A Step Towards a Universal Cross‐Coupling Catalyst
inferred← citeshttps://doi.org/10.1002/chem.200800195openalex-snapshot
Efficient Synthesis of Methylenetetrahydrofurans and Methylenepyrrolidines by Formal [3+2] Cycloadditions of Propargyl Substrates
inferred← citeshttps://doi.org/10.1002/chem.200800608openalex-snapshot
Classical Reagents: New Surprises in Palladium‐Catalyzed CC Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201102285openalex-snapshot
Aryl–Aryl Bond Formation by the Fluoride‐Free Cross‐Coupling of Aryldisiloxanes with Aryl Bromides
inferred← citeshttps://doi.org/10.1002/chem.201103360openalex-snapshot
Cross‐Coupling Reactions of Organosilicon Compounds in the Stereocontrolled Synthesis of Retinoids
inferred← citeshttps://doi.org/10.1002/chem.201200431openalex-snapshot
Palladium‐Catalysed Cross‐Coupling of Vinyldisiloxanes with Benzylic and Allylic Halides and Sulfonates
inferred← citeshttps://doi.org/10.1002/chem.201201806openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Unactivated Alkenes with Acrylates: Application to the Synthesis of the C13–C21 Fragment of Palmerolide A
inferred← citeshttps://doi.org/10.1002/chem.201203337openalex-snapshot
Site‐Selective Deuterated‐Alkene Synthesis with Palladium on Boron Nitride
inferred← citeshttps://doi.org/10.1002/chem.201403255openalex-snapshot
Synthesis of Cyclic Alkenylsiloxanes by Semihydrogenation: A Stereospecific Route to ( Z )‐Alkenyl Polyenes
inferred← citeshttps://doi.org/10.1002/chem.201600420openalex-snapshot
A General Palladium‐Catalyzed Hiyama Cross‐Coupling Reaction of Aryl and Heteroaryl Chlorides
inferred← citeshttps://doi.org/10.1002/chem.201704539openalex-snapshot
2‐(Trimethylsilyl)‐λ3‐Phosphinine: Synthesis, Coordination Chemistry, and Reactivity
inferred← citeshttps://doi.org/10.1002/chem.201802573openalex-snapshot
Pd‐Catalyzed Vinylation of Aryl Halides with Inexpensive Organosilicon Reagents Under Mild Conditions
inferred← citeshttps://doi.org/10.1002/chem.201803213openalex-snapshot
Designing Cross‐Coupling Reactions using Aryl(trialkyl)silanes
inferred← citeshttps://doi.org/10.1002/chem.201902022openalex-snapshot
Pd‐Catalyzed Synthesis of Vinyl Arenes from Aryl Halides and Acrylic Acid
inferred← citeshttps://doi.org/10.1002/chem.202001394openalex-snapshot
Electro‐Olefination—A Catalyst Free Stereoconvergent Strategy for the Functionalization of Alkenes
inferred← citeshttps://doi.org/10.1002/chem.202100084openalex-snapshot
Rhodium‐Catalyzed Intermolecular Silylation of Csp−H by Silacyclobutanes
inferred← citeshttps://doi.org/10.1002/chem.202103078openalex-snapshot
Mechanism‐Based Approach to Reagent Selection for Oxidative Carbon−Hydrogen Bond Cleavage Reactions
inferred← citeshttps://doi.org/10.1002/chem.202300798openalex-snapshot
Highly Chemoselective Zn +2 ‐Catalyzed Hydrosilylation of Alkynes
inferred← citeshttps://doi.org/10.1002/chem.202301259openalex-snapshot
Pt II −N‐Heterocyclic Carbene Complexes in Solvent‐Free Alkene Hydrosilylation
inferred← citeshttps://doi.org/10.1002/chem.202303857openalex-snapshot
An Efficient C−Si/C−H Cross‐Coupling Reaction Enabled by a Radical Pathway
inferred← citeshttps://doi.org/10.1002/chin.198830170openalex-snapshot
ChemInform Abstract: Cross‐Coupling of Organosilanes with Organic Halides Mediated by Palladium Catalyst and Tris(diethylamino)sulfonium Difluorotrimethylsilicate.
inferred← citeshttps://doi.org/10.1002/chin.201023203openalex-snapshot
ChemInform Abstract: Practical Aspects of Carbon—Carbon Cross‐Coupling Reactions Using Heteroarenes
inferred← citeshttps://doi.org/10.1002/chin.201210247openalex-snapshot
ChemInform Abstract: Synthetic Applications of Suzuki—Miyaura Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/cjoc.202100396openalex-snapshot
Oxidative Cross‐Coupling Reactions between Two Nucleophiles †
inferred← citeshttps://doi.org/10.1002/cjoc.70644openalex-snapshot
Diastereoselective Copper‐Catalyzed Defluorosilylation of Pentafluoroethyl Alkenes to Access Polyfluorinated Allylsilanes
inferred← citeshttps://doi.org/10.1002/cplu.201300131openalex-snapshot
An Unexpected Pathway for Ligand Substitution in an Aryl Halide Complex of Palladium
inferred← citeshttps://doi.org/10.1002/cplu.201402153openalex-snapshot
Synthesis of Bright Alkenyl‐1H‐1,2,4‐triazoles: A Theoretical and Photophysical Study
inferred← citeshttps://doi.org/10.1002/ejic.200900115openalex-snapshot
Fluoride‐Free Hiyama and Copper‐ and Amine‐Free Sonogashira Coupling in Air in a Mixed Aqueous Medium by a Series of PEPPSI‐Themed Precatalysts
inferred← citeshttps://doi.org/10.1002/ejic.201200622openalex-snapshot
Studies of the Electronic Properties of N‐Heterocyclic Carbene Ligands in the Context of Homogeneous Catalysis and Bioorganometallic Chemistry
inferred← citeshttps://doi.org/10.1002/ejic.201701321openalex-snapshot
Ethynyl Complexes of Gold(I) Formed by Transmetallation Using Tin(IV) or Silicon(IV) Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.201101110openalex-snapshot
(NHC)Palladium Complexes from Hydroxy‐Functionalized Imidazolium Salts as Catalyst for the Microwave‐Accelerated Fluorine‐Free Hiyama Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201201066openalex-snapshot
NHC‐Ligand Effectiveness in the Fluorine‐Free Hiyama Reaction of Aryl Halides
inferred← citeshttps://doi.org/10.1002/ejoc.201300307openalex-snapshot
Phosphane‐Free Hiyama Cross‐Coupling of Aryl and Heteroaryl Halides Catalyzed by Palladium Nanoparticles in Ionic Liquids
inferred← citeshttps://doi.org/10.1002/ejoc.201301439openalex-snapshot
1,2‐Functionalized Imidazoles as Palladium Ligands: An Efficient and Robust Catalytic System for the Fluorine‐Free Hiyama Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201301802openalex-snapshot
Sequential C3 and C5 Direct C–H Arylation of Imidazo[1,2‐a]pyrazines with (Hetero)aryl Bromides
inferred← citeshttps://doi.org/10.1002/ejoc.201501231openalex-snapshot
Desulfination as an Emerging Strategy in Palladium‐Catalyzed C–C Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201601253openalex-snapshot
Emergence of Unactivated Olefins for the Synthesis of Olefinated Arenes
inferred← citeshttps://doi.org/10.1002/ejoc.201700485openalex-snapshot
Heck‐Like Reactions Involving Heteroatomic Electrophiles
inferred← citeshttps://doi.org/10.1002/ejoc.201701533openalex-snapshot
Regioselective Construction of Functionalized Biarylols by Fe(OTf)3‐Catalyzed Direct Arylation of 1‐Diazonaphthalen‐2(1H)‐ones and Their Fluorescence Properties
inferred← citeshttps://doi.org/10.1002/ejoc.201801153openalex-snapshot
Unprecedented Mechanism of an Organocatalytic Route to Conjugated Enynes with a Junction to Cyclic Nitronates
inferred← citeshttps://doi.org/10.1002/ejoc.202000467openalex-snapshot
Polyethylene Glycol (PEG‐400) as Methylene Spacer and Green Solvent for the Synthesis of Heterodiarylmethanes under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.202200429openalex-snapshot
Ni/g‐C3N4 Photocatalysis: Aerobic Oxidative Coupling Reaction Leading to Amidation of Aldehydes with Amines and C−N, C−O, and C−C Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.202200498openalex-snapshot
Synthesis of Thioalkynes by Desilylative Sonogashira Cross‐Coupling of Aryl Iodides and 1‐Methylthio‐2‐(trimethylsilyl)ethyne
inferred← citeshttps://doi.org/10.1002/gch2.202200240openalex-snapshot
Formal Anti‐Markovnikov Addition of Water to Olefins by Titanocene‐Catalyzed Epoxide Hydrosilylation: From Stoichiometric to Sustainable Catalytic Reactions
inferred← citeshttps://doi.org/10.1002/hc.21481openalex-snapshot
Alkoxy(tetraaryl)silicates bearing 9,10‐disilatriptycene skeleton
inferred← citeshttps://doi.org/10.1002/hlca.19960790118openalex-snapshot
Synthese von ‘Push‐Pull’‐ Eninen
inferred← citeshttps://doi.org/10.1002/ijch.201900143openalex-snapshot
Shuttling Catalyst: Facilitating C−C Bond Formation via Cross‐Couplings with a Thermoresponsive Polymeric Ligand
inferred← citeshttps://doi.org/10.1002/ijch.201900167openalex-snapshot
In Praise of Basic Research as a Vehicle to Practical Applications: Palladium‐Catalyzed Coupling to Form Carbon‐Nitrogen Bonds
inferred← citeshttps://doi.org/10.1002/pola.29256openalex-snapshot
Preparation of stimulus‐responsive, polyfluorene‐wrapped carbon nanotubes via palladium cross coupling
inferred← citeshttps://doi.org/10.1002/slct.201802138openalex-snapshot
Synthesis, In Silico and In Vitro Studies of Potential Glucosamine‐6‐phosphate Synthase and Lanosterol‐14α‐demethylase Inhibitors
inferred← citeshttps://doi.org/10.1002/slct.201900946openalex-snapshot
Rational Design of Sterically Hindered and Unsymmetrical N py N im O ph Pincer‐Type Ligands and Their Palladium(II) Complexes: Catalytic Applications in Suzuki–Miyaura Reaction and Allylation of Aldehydes
inferred← citeshttps://doi.org/10.1002/slct.202103357openalex-snapshot
Recent Advances in the Functionalization of Azulene Through Pd‐Catalyzed Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/slct.202300845openalex-snapshot
Metal‐Free Oxidative Cross‐Dehydrogenative Coupling of Alkenes with Thiophenols
inferred← citeshttps://doi.org/10.1002/slct.202403925openalex-snapshot
Aryl/Hetero‐Aryl Tosylates as Coupling Partners in Metal‐Mediated Suzuki and Hiyama Cross‐Coupling Reactions in Ionic Liquids: Ligand‐Free Facile Synthesis of Biaryls/Heterobiaryls
inferred← citeshttps://doi.org/10.1002/slct.202500428openalex-snapshot
A Review of Design Strategies and Catalytic Applications of Polymer‐Bound Palladium Systems for C─C Bond Formation via Heck and Suzuki Reactions
inferred← citeshttps://doi.org/10.1002/tcr.201600086openalex-snapshot
Cooperative Catalysis of Combined Systems of Transition‐Metal Complexes with Lewis Acids: Theoretical Understanding
inferred← citeshttps://doi.org/10.1002/tcr.20162openalex-snapshot
Selective organic synthesis through generation and reactivity control of hyper‐coordinate metal species
inferred← citeshttps://doi.org/10.1002/tcr.201700022openalex-snapshot
Recent Progress in Application of Graphene Supported Metal Nanoparticles in C−C and C−X Coupling Reactions
inferred← citeshttps://doi.org/10.1002/tcr.201700056openalex-snapshot
Chemistry in Confinement: Copper and Palladium Catalyzed Ecofriendly Organic Transformations within Porous Frameworks
inferred← citeshttps://doi.org/10.1002/tcr.201700069openalex-snapshot
Combination of Tetrabutylammonium Iodide (TBAI) with tert ‐Butyl Hydroperoxide (TBHP): An Efficient Transition‐Metal‐Free System to Construct Various Chemical Bonds
inferred← citeshttps://doi.org/10.1007/3-540-45313-x_1openalex-snapshot
Introduction to Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1007/3-540-45313-x_3openalex-snapshot
Organosilicon Compounds
inferred← citeshttps://doi.org/10.1007/3418_2014_85openalex-snapshot
Ruthenium(II)-Catalysed sp2 C–H Bond Functionalization by C–C Bond Formation
inferred← citeshttps://doi.org/10.1007/7081_2015_162openalex-snapshot
Synthesis of P-, S-, Si-, B-, and Se-Heterocycles via Ring-Closing Metathesis
inferred← citeshttps://doi.org/10.1007/978-3-319-01134-9_3openalex-snapshot
Organotrifluoroborate Coupling
inferred← citeshttps://doi.org/10.1007/978-3-319-33663-3_1openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1007/978-3-642-32368-3_1openalex-snapshot
A Historic Overview of the Metal-Catalyzed Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1007/978-3-662-58104-9_1openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1007/978-981-92-0108-2_10openalex-snapshot
Synthesis and Electronic Properties of π-Conjugated Polymers
inferred← citeshttps://doi.org/10.1007/978-981-99-4121-6_1openalex-snapshot
General Introduction
inferred← citeshttps://doi.org/10.1007/s00706-012-0746-0openalex-snapshot
Recent advances in application of intramolecular Suzuki cross-coupling in cyclization and heterocyclization
inferred← citeshttps://doi.org/10.1007/s00706-012-0838-xopenalex-snapshot
Recent advances in Kumada-Tamao-Corriu cross-coupling reaction catalyzed by different ligands
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