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Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

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What this work says

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

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Dynamic Kinetic Resolution of α,β‐Unsaturated Lactones through Asymmetric Copper‐Catalyzed Conjugate Reduction: Application to the Total Synthesis of Eupomatilone‐3

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What points at this work

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

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Nickel/Tio2-Catalyzed Suzuki–Miyaura Cross-Coupling (Smr) of Aryl Boronic Acids with Aryl Halides in Meoh/H2o

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A Novel Porphyrin-Palladium(0) Functionalized Polyacrylonitrile Fiber as Highly Efficient and Recyclable Heterogeneous Catalyst for the Heck Reaction

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1,1′‐Bis(diphenylphosphino)ferrocene

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Dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II)

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2-(Di-tert-butylphosphino)biphenyl

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Synthesis of Amido‐N‐imidazolium Salts and their Applications as Ligands in Suzuki–Miyaura Reactions: Coupling of Hetero‐ aromatic Halides and the Synthesis of Milrinone and Irbesartan

inferred← citeshttps://doi.org/10.1002/adsc.201000879openalex-snapshot

Gold‐Catalyzed Cyclizations: A Comparative Study of ortho,ortho′‐Substituted KITPHOS Monophosphines with their Biaryl Monophosphine Counterpart SPHOS

inferred← citeshttps://doi.org/10.1002/adsc.201090010openalex-snapshot

Retraction: Iron‐Catalyzed Suzuki–Miyaura Cross‐Coupling Reaction

inferred← citeshttps://doi.org/10.1002/adsc.201100019openalex-snapshot

Oxime Palladacycle‐Catalyzed Suzuki–Miyaura Alkenylation of Aryl, Heteroaryl, Benzyl, and Allyl Chlorides under Microwave Irradiation Conditions

inferred← citeshttps://doi.org/10.1002/adsc.201100140openalex-snapshot

Mechanistic Switch via Subtle Ligand Modulation: Palladium‐Catalyzed Synthesis of α,β‐Substituted Styrenes via CH Bond Functionalization

inferred← citeshttps://doi.org/10.1002/adsc.201100141openalex-snapshot

A Mild Palladium‐Catalyzed Suzuki Coupling Reaction of Quinoline Carboxylates with Boronic Acids

inferred← citeshttps://doi.org/10.1002/adsc.201100725openalex-snapshot

Magnetic Nanoparticles‐Supported Palladium: A Highly Efficient and Reusable Catalyst for the Suzuki, Sonogashira, and Heck Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201100761openalex-snapshot

Ligand‐Free Buchwald–Hartwig Aromatic Aminations of Aryl Halides Catalyzed by Low‐Leaching and Highly Recyclable Sulfur‐Modified Gold‐Supported Palladium Material

inferred← citeshttps://doi.org/10.1002/adsc.201100942openalex-snapshot

Selective Palladium‐Catalyzed Suzuki–Miyaura Reactions of Polyhalogenated Heteroarenes

inferred← citeshttps://doi.org/10.1002/adsc.201100983openalex-snapshot

Beyond the Limits: Palladium‐N‐Heterocyclic Carbene‐Based Catalytic System Enables Highly Efficient [4+2] Benzannulation Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201200095openalex-snapshot

Highly Diastereoselective Synthesis of Atropisomeric Bridged P,N‐Ligands and Their Applications in Asymmetric Suzuki–Miyaura Coupling Reaction

inferred← citeshttps://doi.org/10.1002/adsc.201200243openalex-snapshot

Highly Active Multidentate Alkyne Metathesis Catalysts: Ligand‐Activity Relationship and Their Applications in Efficient Synthesis of Porphyrin‐Based Aryleneethynylene Polymers

inferred← citeshttps://doi.org/10.1002/adsc.201200398openalex-snapshot

An Improved Synthesis of BrettPhos‐ and RockPhos‐Type Biarylphosphine Ligands

inferred← citeshttps://doi.org/10.1002/adsc.201200418openalex-snapshot

Solid‐Supported Rhodium(0) Nano‐/Microparticles: An Efficient Ligand‐Free Heterogeneous Catalyst for Microwave‐Assisted Suzuki–Miyaura Cross‐Coupling Reaction

inferred← citeshttps://doi.org/10.1002/adsc.201200486openalex-snapshot

Catalytic CSe Bond Formation under Very Mild Conditions for the Two‐Step, One‐Pot Synthesis of Aryl Selenoacetates

inferred← citeshttps://doi.org/10.1002/adsc.201200583openalex-snapshot

2‐(1‐Benzotriazolyl)pyridine: A Robust Bidentate Ligand for the Palladium‐Catalyzed CC (Suzuki, Heck, Fujiwara–Moritani, Sonogashira), CN and CS Coupling Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201200619openalex-snapshot

The Clicked Pyridyl‐Triazole Ligand: From Homogeneous to Robust, Recyclable Heterogeneous Mono‐ and Polymetallic Palladium Catalysts for Efficient Suzuki–Miyaura, Sonogashira, and Heck Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201200678openalex-snapshot

Cross‐Coupling in Flow using Supported Catalysts: Mild, Clean, Efficient and Sustainable Suzuki–Miyaura Coupling in a Single Pass

inferred← citeshttps://doi.org/10.1002/adsc.201201085openalex-snapshot

Room Temperature Palladium‐Catalyzed Decarboxylative Acyl/Aroylation using [Fe(III)(EDTA)(η2‐O2)]3− as Oxidant at Biological pH

inferred← citeshttps://doi.org/10.1002/adsc.201201100openalex-snapshot

ortho‐(Dimesitylboryl)phenylphosphines: Positive Boryl Effect in the Palladium‐Catalyzed Suzuki–Miyaura Coupling of 2‐Chloropyridines

inferred← citeshttps://doi.org/10.1002/adsc.201300198openalex-snapshot

An Efficient Route to 3‐Amidylindoles via a Palladium‐ Catalyzed Tandem Reaction of 2‐Alkynylanilines with Isocyanides

inferred← citeshttps://doi.org/10.1002/adsc.201300207openalex-snapshot

Zheda‐Phos for General α‐Monoarylation of Acetone with Aryl Chlorides

inferred← citeshttps://doi.org/10.1002/adsc.201300294openalex-snapshot

Potassium (E)‐Alkenylaryltrifluoroborates: Orthogonal Functionalization of Haloaryltrifluoroborates via Heck–Mizoroki Reaction

inferred← citeshttps://doi.org/10.1002/adsc.201300332openalex-snapshot

Synthesis of Well‐Defined Diphenylvinyl(cyclopropyl)phosphine‐Palladium Complexes for the Suzuki–Miyaura Reaction and Buchwald–Hartwig Amination

inferred← citeshttps://doi.org/10.1002/adsc.201300499openalex-snapshot

Polymer‐Supported Electron‐Rich Oxime Palladacycle as an Efficient Heterogeneous Catalyst for the Suzuki Coupling Reaction

inferred← citeshttps://doi.org/10.1002/adsc.201300567openalex-snapshot

Efficient Synthesis of Dibenzoxaborininols from Diaryl Ethers and Their Application to Dibenzofuran Synthesis

inferred← citeshttps://doi.org/10.1002/adsc.201300776openalex-snapshot

Chemoselective Carbon‐Carbon Cross‐Coupling via Palladium‐Catalyzed Copper‐Mediated CS Cleavage of Disulfides

inferred← citeshttps://doi.org/10.1002/adsc.201300924openalex-snapshot

One‐Pot Tandem Palladium‐Catalyzed Decarboxylative Cross‐Coupling and CH Activation Route to Thienoisoquinolines

inferred← citeshttps://doi.org/10.1002/adsc.201301147openalex-snapshot

Silica‐Supported Tripod Triarylphosphane: Application to Transition Metal‐Catalyzed C(sp3)H Borylations

inferred← citeshttps://doi.org/10.1002/adsc.201400105openalex-snapshot

Palladium‐Catalysed, Directed CH Coupling with Organometallics

inferred← citeshttps://doi.org/10.1002/adsc.201400190openalex-snapshot

Palladium‐Catalyzed Hydrophosphonylation of Alkenes with Dialkyl H‐Phosphonates

inferred← citeshttps://doi.org/10.1002/adsc.201400520openalex-snapshot

Reusable, Highly Active Heterogeneous Palladium Catalyst by Convenient Self‐Encapsulation Cross‐Linking Polymerization for Multiple CarbonCarbon Cross‐Coupling Reactions at ppm to ppb Palladium Loadings

inferred← citeshttps://doi.org/10.1002/adsc.201400679openalex-snapshot

Palladium‐Catalyzed Direct α‐Arylation of Benzyl Thioethers with Aryl Bromides

inferred← citeshttps://doi.org/10.1002/adsc.201500070openalex-snapshot

A Polymer‐Bound Monodentate‐P‐Ligated Palladium Complex as a Recyclable Catalyst for the Suzuki–Miyaura Coupling Reaction of Aryl Chlorides

inferred← citeshttps://doi.org/10.1002/adsc.201500317openalex-snapshot

Diastereoselective Oxidative CN/CO and CN/CN Bond Formation Tandems Initiated by Visible Light: Synthesis of Fused N‐Arylindolines

inferred← citeshttps://doi.org/10.1002/adsc.201500460openalex-snapshot

In Situ Trapped and Immobilized Palladium Nanoparticles as Active and Clean Catalysts for Suzuki–Miyaura Reaction

inferred← citeshttps://doi.org/10.1002/adsc.201500682openalex-snapshot

Handy Protocols using Vinyl Nosylates in Suzuki–Miyaura Cross‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201500844openalex-snapshot

Miyaura Borylation and One‐Pot Two‐Step Homocoupling of Aryl Chlorides and Bromides under Solvent‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.201500846openalex-snapshot

Why Does Industry Not Use Immobilized Transition Metal Complexes as Catalysts?

inferred← citeshttps://doi.org/10.1002/adsc.201500865openalex-snapshot

Palladium‐Catalyzed Two‐Component Domino Coupling Reaction of (Z)‐β‐Bromostyrenes with Norbornenes: Synthesis of 1,5‐Enynes

inferred← citeshttps://doi.org/10.1002/adsc.201700730openalex-snapshot

Base‐Promoted [3+2]‐Annulation of Oxime Esters and Aldehydes for Rapid Isoxazoline Formation

inferred← citeshttps://doi.org/10.1002/adsc.201700810openalex-snapshot

Recent Advances in Palladium‐Catalyzed Cross‐Coupling Reactions at ppm to ppb Molar Catalyst Loadings

inferred← citeshttps://doi.org/10.1002/adsc.201701640openalex-snapshot

A Tunable Route to Prepare α,β‐Unsaturated Esters and α,β‐Unsaturated‐γ‐Keto Esters through Copper‐Catalyzed Coupling of Alkenyl Boronic Acids with Phosphorus Ylides

inferred← citeshttps://doi.org/10.1002/adsc.201800561openalex-snapshot

Heteroatom Donor‐Decorated Polymer‐Immobilized Ionic Liquid Stabilized Palladium Nanoparticles: Efficient Catalysts for Room‐Temperature Suzuki‐Miyaura Cross‐Coupling in Aqueous Media

inferred← citeshttps://doi.org/10.1002/adsc.201901023openalex-snapshot

Metal‐Free Three‐Component Selenopheno[2,3‐ b ]indole Formation through Double C−H Selenylation with Selenium Powder

inferred← citeshttps://doi.org/10.1002/adsc.202000122openalex-snapshot

Suzuki‐Miyaura Cross‐Coupling of Amides using Well‐Defined, Air‐Stable [(PR3)2Pd(II)X2] Precatalysts

inferred← citeshttps://doi.org/10.1002/adsc.202000511openalex-snapshot

Disulfide Promoted C−P Bond Cleavage of Phosphoramide: “P” Surrogates to Synthesize Phosphonates and Phosphinates

inferred← citeshttps://doi.org/10.1002/adsc.202000987openalex-snapshot

Differences in the Performance of Allyl Based Palladium Precatalysts for Suzuki‐Miyaura Reactions

inferred← citeshttps://doi.org/10.1002/adsc.202001211openalex-snapshot

Enantioselective Synthesis of Atropisomeric Biaryls using Biaryl 2,5‐Diphenylphospholanes as Ligands for Palladium‐Catalysed Suzuki‐Miyaura Reactions

inferred← citeshttps://doi.org/10.1002/adsc.202001358openalex-snapshot

Recent Advances in Cross‐Dehydrogenative Couplings (CDC) of C−H Bond in Aqueous Media

inferred← citeshttps://doi.org/10.1002/adsc.202100283openalex-snapshot

Double Ligands Enabled Ruthenium Catalyzed ortho‐C−H Arylation of Dialkyl Biarylphosphines: Straight and Economic Synthesis of Highly Steric and Electron‐Rich Aryl‐Substituted Buchwald‐Type Phosphines

inferred← citeshttps://doi.org/10.1002/adsc.202200321openalex-snapshot

Ylide‐Functionalized Diisopropyl Phosphine (prYPhos): A Ligand for Selective Suzuki‐Miyaura Couplings of Aryl Chlorides

inferred← citeshttps://doi.org/10.1002/adsc.202300650openalex-snapshot

Electrophilic C3−H Alkenylation of 2,6‐Dialkoxypyridine Derivatives via Pd(II)/Tl(III) Reaction System

inferred← citeshttps://doi.org/10.1002/adsc.202301093openalex-snapshot

Catalyst‐Free, Air‐Mediated C(sp2)−H Alkylation of Cyclic Aldimines with Alkylboronic Acids

inferred← citeshttps://doi.org/10.1002/adsc.202301255openalex-snapshot

Palladium‐Catalyzed Chemoselective Amination of Chloro(hetero)aryl Triflates Enabled by Alkyl‐Pyrazole‐Based Phosphine Ligands

inferred← citeshttps://doi.org/10.1002/adsc.202400276openalex-snapshot

Improved Palladium Catalysis in Suzuki‐Type Coupling of Benzotriazinones for o‐Aryl/Alkenyl Benzamides

inferred← citeshttps://doi.org/10.1002/adsc.202400358openalex-snapshot

Palladium (II) Precursors for Clean In Situ Formation of Ad Hoc Cross‐Coupling Catalysts. Their Application in One‐Pot/Two‐Step Catalyses with 2‐Biaryl‐Dialkylphosphine Ligands

inferred← citeshttps://doi.org/10.1002/adsc.202401334openalex-snapshot

Regioselective Cobalt‐Catalyzed Protoboration of Alkynes

inferred← citeshttps://doi.org/10.1002/adsc.202401337openalex-snapshot

Controlling Catalyst Speciation to Achieve Room Temperature Pd‐Catalyzed Aminations with Aryl and Heteroaryl Chlorides

inferred← citeshttps://doi.org/10.1002/adsc.202500270openalex-snapshot

Impact of the Substitution Pattern in N–heterocyclic Olefin‐Substituted Phosphines on Palladium Catalysis

inferred← citeshttps://doi.org/10.1002/adsc.70067openalex-snapshot

A Synthetic Approach to Sterically Hindered P‐Chiral Phosphine Ligands and Their Applications for Asymmetric Gold Catalysis

inferred← citeshttps://doi.org/10.1002/adsc.70243openalex-snapshot

Emergence of Phosphinium Radical Cations as Intermediates for Organic Radical Generation

inferred← citeshttps://doi.org/10.1002/adsc.70298openalex-snapshot

Visible Light‐Induced Disulfidation of Internal Alkynes for Stereoselective Access to ( E )‐Vinyl Sulfides

inferred← citeshttps://doi.org/10.1002/adsc.70609openalex-snapshot

Bulky Monophosphine Ligand Synthesis by Nucleophilic Addition to Peri ‐Functionalized Phosphine Isoindolium Salts

inferred← citeshttps://doi.org/10.1002/adsc.70631openalex-snapshot

Orthogonal One‐Pot Dual Catalysis Enabled by a Hybrid Chiral Diene/Phosphine Ligand

inferred← citeshttps://doi.org/10.1002/adsc.70663openalex-snapshot

High‐Throughput Experimentation‐Assisted Optimization of the Suzuki–Miyaura Coupling Using Palladium– N ‐Heterocyclic Carbene Precatalysts

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/advs.201901551openalex-snapshot

DNA‐Encoded Libraries: Aryl Fluorosulfonates as Versatile Electrophiles Enabling Facile On‐DNA Suzuki, Sonogashira, and Buchwald Reactions

inferred← citeshttps://doi.org/10.1002/advs.202201000openalex-snapshot

Synthesis of Defective Nanographenes Containing Joined Pentagons and Heptagons

inferred← citeshttps://doi.org/10.1002/advs.202519731openalex-snapshot

A Generalized Approach for Distal C–H Arylation of Organic Building Blocks: Unveiling the Role of Counter Anion

inferred← citeshttps://doi.org/10.1002/agt2.650openalex-snapshot

General method to synthesize aggregation‐induced emission molecules via carbon‐sulfur bond activation

inferred← citeshttps://doi.org/10.1002/ajoc.201402035openalex-snapshot

CC Coupling Through Intramolecular Dual CH Activation Directed by a Removable Carboxylate Group: A Method for the Synthesis of Fluorenones under Mild Reaction Conditions

inferred← citeshttps://doi.org/10.1002/ajoc.201500532openalex-snapshot

Contorted Arene‐fused Metallophthalocyanines

inferred← citeshttps://doi.org/10.1002/ajoc.201600319openalex-snapshot

Palladium‐Catalyzed Suzuki–Miyaura Coupling Reactions of Boronic Acid Derivatives with Aryl Chlorides

inferred← citeshttps://doi.org/10.1002/ajoc.201600606openalex-snapshot

Surfactant‐Assisted Suzuki–Miyaura Coupling Reaction of Unreactive Chlorobenzene over Hydrotalcite‐Supported Palladium Catalyst

inferred← citeshttps://doi.org/10.1002/ajoc.201700064openalex-snapshot

Pd(PPh3)4‐Catalyzed Buchwald–Hartwig Amination ofAryl Fluorosulfonates with Aryl Amines

inferred← citeshttps://doi.org/10.1002/ajoc.201700068openalex-snapshot

C(sp2)−C(sp2) Coupling in Water: Palladium(II) Complexes of N‐Pincer Tetradentate Porphyrins as Effective Catalysts

inferred← citeshttps://doi.org/10.1002/ajoc.201700323openalex-snapshot

Robust Palladium‐Catalyzed Arylation of Catalyst‐Poisoning ortho‐Sulfanyl Aryl Halides with Tetraarylborates and Its Application to Synthesis of π‐Extended Dibenzothiophenes

inferred← citeshttps://doi.org/10.1002/ajoc.201800001openalex-snapshot

Synthesis of N‐Heterocyclic Carbene–PdII–2‐Methyl‐4,5‐dihydrooxazole Complexes and Their Application Toward Highly Chemoselective Mono‐Suzuki–Miyaura Coupling of Dichlorobenzenes

inferred← citeshttps://doi.org/10.1002/ajoc.201800002openalex-snapshot

Copper‐Catalyzed Direct C−H Bond Arylation of Benzoxazoles with Anilines

inferred← citeshttps://doi.org/10.1002/ajoc.201900163openalex-snapshot

Catalytic Strategies to Convert 2‐Halopyridines to 2‐Alkylpyridines

inferred← citeshttps://doi.org/10.1002/ajoc.201900615openalex-snapshot

Hydroboration of Alkenes and Alkynes Employing Earth‐Abundant Metal Catalysts

inferred← citeshttps://doi.org/10.1002/ajoc.202000308openalex-snapshot

Recent Advances in the Synthesis of Tamoxifen and Analogues in Medicinal Chemistry

inferred← citeshttps://doi.org/10.1002/ajoc.202100161openalex-snapshot

Solvent‐Free Ruthenium‐Catalyzed Direct Coupling of Phosphines and Aryl Chlorides via C−H Activation: An Efficient and Straight Access to Aryl‐Substituted Biarylphosphines

inferred← citeshttps://doi.org/10.1002/ajoc.202100223openalex-snapshot

The Chemistry and Biological Applications of 3H‐Pyrrolo[2,3‐c]quinolines and Marinoquinolines

inferred← citeshttps://doi.org/10.1002/ajoc.202400011openalex-snapshot

Highly Ordered Mesoporous Polymer‐Supported Phosphine as the Ligand for Organometallic Reaction: Suzuki‐Miyaura Cross‐Coupling of Aryl Chlorides at Room Temperature

inferred← citeshttps://doi.org/10.1002/ange.200804517openalex-snapshot

Palladiumkatalysierte direkte Arylierungen von Heteroarenen mit Tosylaten und Mesylaten

inferred← citeshttps://doi.org/10.1002/ange.200900435openalex-snapshot

Structure and Reactivity of a Unique Y‐Shaped Tricoordinate Bis(silyl)platinum(II)–NHC Complex

inferred← citeshttps://doi.org/10.1002/ange.200902148openalex-snapshot

Palladium‐Catalyzed Hydroxylation of Aryl Halides under Ambient Conditions

inferred← citeshttps://doi.org/10.1002/ange.200902617openalex-snapshot

Selective Synthesis of [12]Cycloparaphenylene

inferred← citeshttps://doi.org/10.1002/ange.200903158openalex-snapshot

Room‐Temperature Copper‐Catalyzed Carbon–Nitrogen Coupling of Aryl Iodides and Bromides Promoted by Organic Ionic Bases

inferred← citeshttps://doi.org/10.1002/ange.200903500openalex-snapshot

Rhodium/N‐Heterocyclic Carbene Catalyzed Direct Intermolecular Arylation of sp2 and sp3 CH Bonds with Chelation Assistance

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.200904306openalex-snapshot

Organotrifluorborate und einfach koordinierte Palladiumkomplexe als Katalysatoren – die perfekte Kombination für die Suzuki‐Miyaura‐Kupplung

inferred← citeshttps://doi.org/10.1002/ange.200904615openalex-snapshot

Stereoselektive Synthese von β‐Chlorvinyl‐substituierten Ketonen und Arenen durch katalytische Addition von Säurechloriden an Alkine

inferred← citeshttps://doi.org/10.1002/ange.200905402openalex-snapshot

Rhodium‐Catalyzed Asymmetric Intramolecular Hydroamination of Unactivated Alkenes

inferred← citeshttps://doi.org/10.1002/ange.200905626openalex-snapshot

A Practical Heterogeneous Catalyst for the Suzuki, Sonogashira, and Stille Coupling Reactions of Unreactive Aryl Chlorides

inferred← citeshttps://doi.org/10.1002/ange.200905953openalex-snapshot

Decarboxylative Cross‐Coupling of Aryl Tosylates with Aromatic Carboxylate Salts

inferred← citeshttps://doi.org/10.1002/ange.201000460openalex-snapshot

Palladium‐Catalyzed Aerobic Oxidative Carbonylation of Arylboronate Esters under Mild Conditions

inferred← citeshttps://doi.org/10.1002/ange.201000576openalex-snapshot

A Highly Active Heterogeneous Palladium Catalyst for the Suzuki–Miyaura and Ullmann Coupling Reactions of Aryl Chlorides in Aqueous Media

inferred← citeshttps://doi.org/10.1002/ange.201001522openalex-snapshot

Aryl Trifluoroborates in Suzuki–Miyaura Coupling: The Roles of Endogenous Aryl Boronic Acid and Fluoride

inferred← citeshttps://doi.org/10.1002/ange.201001787openalex-snapshot

Wiederverwendbare Katalysatoren für palladiumkatalysierte C‐O‐Kupplungen, Buchwald‐Hartwig‐Aminierungen und Sonogashira‐Reaktionen

inferred← citeshttps://doi.org/10.1002/ange.201002404openalex-snapshot

A General and Special Catalyst for Suzuki–Miyaura Coupling Processes

inferred← citeshttps://doi.org/10.1002/ange.201004051openalex-snapshot

Übergangsmetallkatalysierte Trifluormethylierung von Arylhalogeniden

inferred← citeshttps://doi.org/10.1002/ange.201004911openalex-snapshot

A Simple and General Platform for Generating Stereochemically Complex Polyene Frameworks by Iterative Cross‐Coupling

inferred← citeshttps://doi.org/10.1002/ange.201005142openalex-snapshot

Passive F+‐Oxidationsmittel ermöglichen die selektive reduktive Eliminierung hochvalenter Metallzentren in der Katalyse

inferred← citeshttps://doi.org/10.1002/ange.201005734openalex-snapshot

A Modular and Size‐Selective Synthesis of [n]Cycloparaphenylenes: A Step toward the Selective Synthesis of [n,n] Single‐Walled Carbon Nanotubes

inferred← citeshttps://doi.org/10.1002/ange.201100763openalex-snapshot

Oxidative Carbonylierungen: Organometallverbindungen (RM) oder Kohlenwasserstoffe (RH) als Nucleophile

inferred← citeshttps://doi.org/10.1002/ange.201101191openalex-snapshot

Nickel‐Catalyzed Cross‐Coupling of Styrenyl Epoxides with Boronic Acids

inferred← citeshttps://doi.org/10.1002/ange.201101480openalex-snapshot

Suzuki–Miyaura Cross‐Coupling Reactions in Flow: Multistep Synthesis Enabled by a Microfluidic Extraction

inferred← citeshttps://doi.org/10.1002/ange.201103074openalex-snapshot

Lewis‐Säure‐vermittelte benzylische Kreuzkupplungen von Pyridinen mit Arylbromiden

inferred← citeshttps://doi.org/10.1002/ange.201105223openalex-snapshot

Continuous‐Flow Synthesis of Biaryls Enabled by Multistep Solid‐Handling in a Lithiation/Borylation/Suzuki–Miyaura Cross‐Coupling Sequence

inferred← citeshttps://doi.org/10.1002/ange.201106742openalex-snapshot

Palladium‐Catalyzed 2,2,2‐Trifluoroethylation of Organoboronic Acids and Esters

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.201108511openalex-snapshot

Chirale einzähnige Phosphine und sperrige Carbonsäuren: kooperative Effekte in Pd‐katalysierten enantioselektiven C(sp3)‐H‐Funktionalisierungen

inferred← citeshttps://doi.org/10.1002/ange.201200153openalex-snapshot

A General Pd‐Catalyzed Decarboxylative Cross‐Coupling Reaction between Aryl Carboxylic Acids: Synthesis of Biaryl Compounds

inferred← citeshttps://doi.org/10.1002/ange.201201529openalex-snapshot

Copper‐Catalyzed Tandem CN Bond Formation: An Efficient Annulative Synthesis of Functionalized Cinnolines

inferred← citeshttps://doi.org/10.1002/ange.201203093openalex-snapshot

Concise Total Synthesis of (−)‐Myxalamide A

inferred← citeshttps://doi.org/10.1002/ange.201203180openalex-snapshot

Total Synthesis of Neurymenolide A Based on a Gold‐Catalyzed Synthesis of 4‐Hydroxy‐2‐pyrones

inferred← citeshttps://doi.org/10.1002/ange.201207428openalex-snapshot

Highly Reactive, Single‐Component Nickel Catalyst Precursor for Suzuki–Miyuara Cross‐Coupling of Heteroaryl Boronic Acids with Heteroaryl Halides

inferred← citeshttps://doi.org/10.1002/ange.201208025openalex-snapshot

Decarboxylierende Kreuzkupplung von Mesylaten katalysiert durch ein Kupfer/Palladium‐System mit maßgeschneiderten Imidazolylphosphanliganden

inferred← citeshttps://doi.org/10.1002/ange.201303188openalex-snapshot

Water‐Stabilized Three‐ and Four‐Atom Palladium Clusters as Highly Active Catalytic Species in Ligand‐Free CC Cross‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/ange.201306007openalex-snapshot

Cascade Palladium Catalysis: A Predictable and Selectable Regiocontrolled Synthesis of N‐Arylbenzimidazoles

inferred← citeshttps://doi.org/10.1002/ange.201306769openalex-snapshot

Threefold Cross‐Linked Polystyrene–Triphenylphosphane Hybrids: Mono‐P‐Ligating Behavior and Catalytic Applications for Aryl Chloride Cross‐Coupling and C(sp3)H Borylation

inferred← citeshttps://doi.org/10.1002/ange.201309546openalex-snapshot

Site‐Differentiated Polyboron Arenes Prepared by Direct CH Borylation and Their Highly Selective Suzuki–Miyaura Cross‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/ange.201310275openalex-snapshot

Copper‐Catalyzed Cross‐Coupling of Boronic Esters with Aryl Iodides and Application to the Carboboration of Alkynes and Allenes

inferred← citeshttps://doi.org/10.1002/ange.201403793openalex-snapshot

Palladium‐Catalyzed Cascade CH Trifluoroethylation of Aryl Iodides and Heck Reaction: Efficient Synthesis of ortho‐Trifluoroethylstyrenes

inferred← citeshttps://doi.org/10.1002/ange.201404912openalex-snapshot

A Polyphenylene Support for Pd Catalysts with Exceptional Catalytic Activity

inferred← citeshttps://doi.org/10.1002/ange.201406479openalex-snapshot

Dehydrogenative N‐Incorporation: A Direct Approach to Quinoxaline N‐Oxides under Mild Conditions

inferred← citeshttps://doi.org/10.1002/ange.201407586openalex-snapshot

Copper‐Catalyzed Coupling of Triaryl‐ and Trialkylindium Reagents with Aryl Iodides and Bromides through Consecutive Transmetalations

inferred← citeshttps://doi.org/10.1002/ange.201408121openalex-snapshot

Iron‐Induced Regio‐ and Stereoselective Addition of Sulfenyl Chlorides to Alkynes by a Radical Pathway

inferred← citeshttps://doi.org/10.1002/ange.201411518openalex-snapshot

Efficient Synthesis of Sterically Hindered Arenes Bearing Acyclic Secondary Alkyl Groups by Suzuki–Miyaura Cross‐Couplings

inferred← citeshttps://doi.org/10.1002/ange.201500201openalex-snapshot

Palladium‐Catalyzed Enantioselective CH Arylation for the Synthesis of P‐Stereogenic Compounds

inferred← citeshttps://doi.org/10.1002/ange.201502502openalex-snapshot

Nickel‐Catalyzed Cross‐Coupling Reactions of o‐Carboranyl with Aryl Iodides: Facile Synthesis of 1‐Aryl‐o‐Carboranes and 1,2‐Diaryl‐o‐Carboranes

inferred← citeshttps://doi.org/10.1002/ange.201503476openalex-snapshot

London’sche Dispersionswechselwirkungen in der Molekülchemie – eine Neubetrachtung sterischer Effekte

inferred← citeshttps://doi.org/10.1002/ange.201504481openalex-snapshot

Palladium‐Catalyzed Direct Dialkenylation of Cage BH Bonds in o‐Carboranes through Cross‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/ange.201504993openalex-snapshot

Imidazolin‐2‐ylidenaminophosphane als sehr elektronenreiche Liganden für Übergangsmetallkatalysatoren

inferred← citeshttps://doi.org/10.1002/ange.201505699openalex-snapshot

Comparison of dppf‐Supported Nickel Precatalysts for the Suzuki–Miyaura Reaction: The Observation and Activity of Nickel(I)

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