On the public citation graph
Alkyl−Alkyl Suzuki Cross-Couplings of Unactivated Secondary Alkyl Halides at Room Temperature
0 signed · 269 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200461432openalex-snapshot
Catalysts for Cross‐Coupling Reactions with Non‐activated Alkyl Halides
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/10.1021/ja0389366openalex-snapshot
Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides
inferredcites →https://doi.org/10.1021/ja039889kopenalex-snapshot
Suzuki Cross-Couplings of Unactivated Secondary Alkyl Bromides and Iodides
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/jo971681sopenalex-snapshot
Alkylboranes in the Suzuki−Miyaura Coupling: Stereochemical and Mechanistic Studies
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.4686085openalex-extracted
Evaluation of Hemilabile Pd(Ii) Nns and Nnse Non-Symmetric Pincers in Suzuki-Miyaura Cross-Coupling: Unexpected Selective Nitrile Hydration of 4-Bromonitrobenzene in Mild Conditions
inferred← citeshttps://doi.org/10.1002/047084289x.rn01428openalex-snapshot
Nickel(II) Chloride Ethylene Glycol Dimethyl Ether Complex
inferred← citeshttps://doi.org/10.1002/047084289x.rn02388openalex-snapshot
trans ‐ N 1 , N 2 ‐Dimethyl‐1,2‐Cyclohexanediamine
inferred← citeshttps://doi.org/10.1002/0471264180.or100.08openalex-snapshot
Carbon–Carbon Bond Formation by Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1002/0471264180.or113.01openalex-snapshot
Transition‐Metal‐Catalyzed Alkyl–Alkyl Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527628698.hgc052openalex-snapshot
Coupling Reactions in Water
inferred← citeshttps://doi.org/10.1002/9783527639328.ch4openalex-snapshot
The Contemporary Suzuki–Miyaura Reaction
inferred← citeshttps://doi.org/10.1002/9783527655588.ch2openalex-snapshot
State‐of‐the‐Art in Metal‐Catalyzed Cross‐Coupling Reactions of Organoboron Compounds with Organic Electrophiles
inferred← citeshttps://doi.org/10.1002/9783527664801.ch9openalex-snapshot
An Overview of Recent Developments in Metal‐Catalyzed Asymmetric Transformations
inferred← citeshttps://doi.org/10.1002/9783527826445.ch3openalex-snapshot
Copper‐Catalyzed Cross‐Coupling Reactions of Organoboron Compounds
inferred← citeshttps://doi.org/10.1002/adsc.200800166openalex-snapshot
Cobalt‐Catalyzed Cross‐Coupling Reaction between Functionalized Primary and Secondary Alkyl Halides and Aliphatic Grignard Reagents
inferred← citeshttps://doi.org/10.1002/adsc.201100134openalex-snapshot
A Highly Active and Recyclable Catalyst: Phosphine Dendrimer‐Stabilized Nickel Nanoparticles for the Suzuki Coupling Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201200136openalex-snapshot
Alkylboronic Esters from Palladium‐ and Nickel‐Catalyzed Borylation of Primary and Secondary Alkyl Bromides
inferred← citeshttps://doi.org/10.1002/adsc.201200821openalex-snapshot
Rhodium(I)‐Catalyzed Arylation of β‐Chloro Ketones and Related Derivatives through Domino Dehydrochlorination/ Conjugate Addition
inferred← citeshttps://doi.org/10.1002/adsc.201800826openalex-snapshot
Mild Base Promoted Nucleophilic Substitution of Unactivated sp3‐Carbon Electrophiles with Alkenylboronic Acids
inferred← citeshttps://doi.org/10.1002/ange.200801447openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryl Methyl Ethers with Aryl Boronic Esters
inferred← citeshttps://doi.org/10.1002/ange.200803509openalex-snapshot
Asymmetrische Kreuzkupplung von nicht‐aktivierten sekundären Alkylhalogeniden
inferred← citeshttps://doi.org/10.1002/ange.200803611openalex-snapshot
Sekundäre Alkylhalogenide in übergangsmetallkatalysierten Kreuzkupplungen
inferred← citeshttps://doi.org/10.1002/ange.200806138openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Non‐activated and Functionalized Alkyl Halides with Alkyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/ange.200806273openalex-snapshot
Palladium(II)‐katalysierte C‐H‐Aktivierung/C‐C‐Kreuzkupplung: Vielseitigkeit und Anwendbarkeit
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.201001787openalex-snapshot
Wiederverwendbare Katalysatoren für palladiumkatalysierte C‐O‐Kupplungen, Buchwald‐Hartwig‐Aminierungen und Sonogashira‐Reaktionen
inferred← citeshttps://doi.org/10.1002/ange.201002116openalex-snapshot
Zinc Chloride Enhanced Arylations of Secondary Benzyl Trifluoroacetates in the Presence of β‐Hydrogen Atoms
inferred← citeshttps://doi.org/10.1002/ange.201003272openalex-snapshot
Alkyl–Alkyl Suzuki Cross‐Coupling of Unactivated Secondary Alkyl Chlorides
inferred← citeshttps://doi.org/10.1002/ange.201007963openalex-snapshot
Strategien und Taktiken für die metallgesteuerte Synthese von Rotaxanen, Knoten, Catenanen und Verschlingungen höherer Ordnung
inferred← citeshttps://doi.org/10.1002/ange.201008007openalex-snapshot
Copper‐Catalyzed Cross‐Coupling Reaction of Organoboron Compounds with Primary Alkyl Halides and Pseudohalides
inferred← citeshttps://doi.org/10.1002/ange.201101769openalex-snapshot
Carboxylation of Alkylboranes by N‐Heterocyclic Carbene Copper Catalysts: Synthesis of Carboxylic Acids from Terminal Alkenes and Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/ange.201107376openalex-snapshot
Porous Single‐Crystalline Palladium Nanoparticles with High Catalytic Activities
inferred← citeshttps://doi.org/10.1002/ange.201204275openalex-snapshot
Copper‐Catalyzed Cross‐Coupling of Functionalized Alkyl Halides and Tosylates with Secondary and Tertiary Alkyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/ange.201208203openalex-snapshot
Sterically Controlled Alkylation of Arenes through Iridium‐Catalyzed CH Borylation
inferred← citeshttps://doi.org/10.1002/ange.201311323openalex-snapshot
Palladium‐Catalyzed Heck‐Type Cross‐Couplings of Unactivated Alkyl Iodides
inferred← citeshttps://doi.org/10.1002/ange.201503297openalex-snapshot
Nickel‐Catalyzed Alkyl–Alkyl Cross‐Couplings of Fluorinated Secondary Electrophiles: A General Approach to the Synthesis of Compounds having a Perfluoroalkyl Substituent
inferred← citeshttps://doi.org/10.1002/ange.201706719openalex-snapshot
Nickel‐Catalyzed Enantioselective Conjunctive Cross‐Coupling of 9‐BBN Borates
inferred← citeshttps://doi.org/10.1002/ange.201712731openalex-snapshot
NiH‐Catalyzed Reductive Relay Hydroalkylation: A Strategy for the Remote C(sp3)−H Alkylation of Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201804684openalex-snapshot
Synthesis of Secondary and Tertiary Alkyl Boronic Esters by gem‐Carboborylation: Carbonyl Compounds as Bis(electrophile) Equivalents
inferred← citeshttps://doi.org/10.1002/ange.202103327openalex-snapshot
Direct Synthesis of Ketones from Methyl Esters by Nickel‐Catalyzed Suzuki–Miyaura Coupling
inferred← citeshttps://doi.org/10.1002/ange.202112454openalex-snapshot
The Formal Cross‐Coupling of Amines and Carboxylic Acids to Form sp3–sp3 Carbon–Carbon Bonds
inferred← citeshttps://doi.org/10.1002/ange.202307602openalex-snapshot
Chemoenzymatic Synthesis of Cylindrocyclophanes A and F and Merocyclophanes A and D
inferred← citeshttps://doi.org/10.1002/ange.202311941openalex-snapshot
Electrochemical NiH‐Catalyzed C(sp3)−C(sp3) Coupling of Alkyl Halides and Alkyl Alkenes
inferred← citeshttps://doi.org/10.1002/anie.200801447openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryl Methyl Ethers with Aryl Boronic Esters
inferred← citeshttps://doi.org/10.1002/anie.200803509openalex-snapshot
Asymmetric Cross‐Coupling of Non‐Activated Secondary Alkyl Halides
inferred← citeshttps://doi.org/10.1002/anie.200803611openalex-snapshot
Secondary Alkyl Halides in Transition‐Metal‐Catalyzed Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.200806138openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Non‐activated and Functionalized Alkyl Halides with Alkyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/anie.200806273openalex-snapshot
Palladium(II)‐Catalyzed CH Activation/CC Cross‐Coupling Reactions: Versatility and Practicality
inferred← citeshttps://doi.org/10.1002/anie.200905626openalex-snapshot
A Practical Heterogeneous Catalyst for the Suzuki, Sonogashira, and Stille Coupling Reactions of Unreactive Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/anie.201001787openalex-snapshot
Recyclable Catalysts for Palladium‐Catalyzed CO Coupling Reactions, Buchwald–Hartwig Aminations, and Sonogashira Reactions
inferred← citeshttps://doi.org/10.1002/anie.201002116openalex-snapshot
Zinc Chloride Enhanced Arylations of Secondary Benzyl Trifluoroacetates in the Presence of β‐Hydrogen Atoms
inferred← citeshttps://doi.org/10.1002/anie.201003272openalex-snapshot
Alkyl–Alkyl Suzuki Cross‐Coupling of Unactivated Secondary Alkyl Chlorides
inferred← citeshttps://doi.org/10.1002/anie.201007963openalex-snapshot
Strategies and Tactics for the Metal‐Directed Synthesis of Rotaxanes, Knots, Catenanes, and Higher Order Links
inferred← citeshttps://doi.org/10.1002/anie.201008007openalex-snapshot
Copper‐Catalyzed Cross‐Coupling Reaction of Organoboron Compounds with Primary Alkyl Halides and Pseudohalides
inferred← citeshttps://doi.org/10.1002/anie.201101769openalex-snapshot
Carboxylation of Alkylboranes by N‐Heterocyclic Carbene Copper Catalysts: Synthesis of Carboxylic Acids from Terminal Alkenes and Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/anie.201107376openalex-snapshot
Porous Single‐Crystalline Palladium Nanoparticles with High Catalytic Activities
inferred← citeshttps://doi.org/10.1002/anie.201204275openalex-snapshot
Copper‐Catalyzed Cross‐Coupling of Functionalized Alkyl Halides and Tosylates with Secondary and Tertiary Alkyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/anie.201208203openalex-snapshot
Sterically Controlled Alkylation of Arenes through Iridium‐Catalyzed CH Borylation
inferred← citeshttps://doi.org/10.1002/anie.201311323openalex-snapshot
Palladium‐Catalyzed Heck‐Type Cross‐Couplings of Unactivated Alkyl Iodides
inferred← citeshttps://doi.org/10.1002/anie.201503297openalex-snapshot
Nickel‐Catalyzed Alkyl–Alkyl Cross‐Couplings of Fluorinated Secondary Electrophiles: A General Approach to the Synthesis of Compounds having a Perfluoroalkyl Substituent
inferred← citeshttps://doi.org/10.1002/anie.201706719openalex-snapshot
Nickel‐Catalyzed Enantioselective Conjunctive Cross‐Coupling of 9‐BBN Borates
inferred← citeshttps://doi.org/10.1002/anie.201712731openalex-snapshot
NiH‐Catalyzed Reductive Relay Hydroalkylation: A Strategy for the Remote C(sp 3 )−H Alkylation of Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201804684openalex-snapshot
Synthesis of Secondary and Tertiary Alkyl Boronic Esters by gem ‐Carboborylation: Carbonyl Compounds as Bis(electrophile) Equivalents
inferred← citeshttps://doi.org/10.1002/anie.202103327openalex-snapshot
Direct Synthesis of Ketones from Methyl Esters by Nickel‐Catalyzed Suzuki–Miyaura Coupling
inferred← citeshttps://doi.org/10.1002/anie.202112454openalex-snapshot
The Formal Cross‐Coupling of Amines and Carboxylic Acids to Form sp 3 –sp 3 Carbon–Carbon Bonds
inferred← citeshttps://doi.org/10.1002/anie.202307602openalex-snapshot
Chemoenzymatic Synthesis of Cylindrocyclophanes A and F and Merocyclophanes A and D
inferred← citeshttps://doi.org/10.1002/anie.202311941openalex-snapshot
Electrochemical NiH‐Catalyzed C(sp 3 )−C(sp 3 ) Coupling of Alkyl Halides and Alkyl Alkenes
inferred← citeshttps://doi.org/10.1002/aoc.1795openalex-snapshot
A Suzuki‐type cross‐coupling reaction of arylacetylene halides with arylboronic acids
inferred← citeshttps://doi.org/10.1002/aoc.3020openalex-snapshot
BiCl3‐catalyzed carbon‒carbon cross‐coupling of organoboronic acids with aryl iodides
inferred← citeshttps://doi.org/10.1002/aoc.3095openalex-snapshot
A highly selective synthesis of 1‐substituted (E)‐buta‐1,3‐dienes with 4,4,5,5‐tetramethyl‐2‐vinyl‐1,3,2‐dioxaborolane as building block
inferred← citeshttps://doi.org/10.1002/aoc.3691openalex-snapshot
Highly stable magnetically separable copper nanocatalyst as an efficient catalyst for C(sp2)–C(sp) and C(sp2)–C(sp2) cross‐coupling reactions
inferred← citeshttps://doi.org/10.1002/aoc.4302openalex-snapshot
Palladium nanoparticles immobilized on EDTA‐modified Fe3O4@SiO2 nanospheres as an efficient and magnetically separable catalyst for Suzuki and Sonogashira cross‐coupling reactions
inferred← citeshttps://doi.org/10.1002/aoc.4909openalex-snapshot
Palladium nanoparticles‐decorated triethanolammonium chloride ionic liquid‐modified TiO2 nanoparticles (TiO2/IL‐Pd): A highly active and recoverable catalyst for Suzuki–Miyaura cross‐coupling reaction in aqueous medium
inferred← citeshttps://doi.org/10.1002/asia.202200836openalex-snapshot
Iron Catalysis: A New Horizon Towards Organoboron‐mediated C−C Cross‐coupling
inferred← citeshttps://doi.org/10.1002/asia.202400126openalex-snapshot
Controllable Chemoselectivity Cascade Reactions for the Synthesis of Phenanthrenols via Palladium‐Catalyzed‐Suzuki/Heck Reaction and Michael Addition
inferred← citeshttps://doi.org/10.1002/chem.200802059openalex-snapshot
Nickel Complexes of a Pincer Amidobis(amine) Ligand: Synthesis, Structure, and Activity in Stoichiometric and Catalytic CC Bond‐Forming Reactions of Alkyl Halides
inferred← citeshttps://doi.org/10.1002/chem.201001631openalex-snapshot
Palladium‐ and Nickel‐Catalyzed Direct Alkylation of Azoles with Unactivated Alkyl Bromides and Chlorides
inferred← citeshttps://doi.org/10.1002/chem.201103882openalex-snapshot
Theoretical Study on the Mechanism of Ni‐Catalyzed Alkyl–Alkyl Suzuki Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/chem.201300882openalex-snapshot
Ni‐Catalyzed Cascade Cyclization–Kumada Alkyl–Alkyl Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/chem.201301350openalex-snapshot
Nickel‐Catalyzed Direct Alkylation of Heterocycles with α‐Bromo Carbonyl Compounds: C3‐Selective Functionalization of 2‐Pyridones
inferred← citeshttps://doi.org/10.1002/chem.201406591openalex-snapshot
Modular Stereoselective Synthesis of (1→2)‐C‐Glycosides based on the sp2–sp3 Suzuki–Miyaura Reaction
inferred← citeshttps://doi.org/10.1002/chem.201500110openalex-snapshot
Computational Insight into Nickel‐Catalyzed Carbon–Carbon versus Carbon–Boron Coupling Reactions of Primary, Secondary, and Tertiary Alkyl Bromides
inferred← citeshttps://doi.org/10.1002/chem.201501543openalex-snapshot
Cobalt‐Catalyzed Cross‐Coupling of 3‐ and 4‐Iodopiperidines with Grignard Reagents
inferred← citeshttps://doi.org/10.1002/chem.201602486openalex-snapshot
Formation of C(sp3)–C(sp3) Bonds through Nickel‐Catalyzed Decarboxylative Olefin Hydroalkylation Reactions
inferred← citeshttps://doi.org/10.1002/chem.201905591openalex-snapshot
Cp*RhIII‐Catalyzed Sterically Controlled C(sp3)−H Selective Mono‐ and Diarylation of 8‐Methylquinolines with Organoborons**
inferred← citeshttps://doi.org/10.1002/chem.202005397openalex-snapshot
One‐Pot Dual C−C Coupling Reaction via Site Selective Cascade Formation by PdII‐Cryptate of an Amino‐Ether Heteroditopic Macrobicycle
inferred← citeshttps://doi.org/10.1002/chin.200752050openalex-snapshot
Alkyl—Alkyl Suzuki Cross‐Couplings of Unactivated Secondary Alkyl Halides at Room Temperature.
inferred← citeshttps://doi.org/10.1002/cjoc.200890401openalex-snapshot
Reusable and Ligand‐Free Palladium‐Catalyzed Suzuki‐Miyaura Cross‐Couplings of Aryl Halides with Arylboronic Acids in Tetra‐n‐butylammonium Bromide
inferred← citeshttps://doi.org/10.1002/cjoc.201100544openalex-snapshot
An Efficient Palladium and Bis(2‐pyridylmethyl)amine‐based System for Suzuki‐Miyaura Cross‐Coupling under Aqueous and Aerobic Condition
inferred← citeshttps://doi.org/10.1002/cssc.200800042openalex-snapshot
A Highly Active Water‐Soluble Cross‐Coupling Catalyst Based on Dendritic Polyglycerol N‐Heterocyclic Carbene Palladium Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.200900538openalex-snapshot
A General and Efficient Suzuki–Miyaura Cross‐Coupling Protocol Using Weak Base and No Water: The Essential Role of Acetate
inferred← citeshttps://doi.org/10.1002/ejoc.201200350openalex-snapshot
Application of LB‐Phos·HBF4 in the Suzuki Coupling Reaction of 2‐Bromoalken‐3‐ols with Alkylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201402108openalex-snapshot
Total Synthesis of (±)‐Paroxetine by Diastereoconvergent Cobalt‐Catalysed Arylation
inferred← citeshttps://doi.org/10.1002/ejoc.201403007openalex-snapshot
Nickel‐Catalyzed Kumada Coupling of Benzyl Chlorides and Vinylogous Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202100361openalex-snapshot
Transition Metal‐Free sp3−sp3 Carbon‐Carbon Coupling between Benzylboronic Esters and Alkyl Bromides
inferred← citeshttps://doi.org/10.1002/ijch.201000038openalex-snapshot
Cross‐Coupling of C(sp3)–H Bonds with Organometallic Reagents via Pd(II)/Pd(0) Catalysis
inferred← citeshttps://doi.org/10.1002/ijch.201900087openalex-snapshot
Transition‐Metal‐Catalyzed 1,2‐Carboboration of Alkenes: Strategies, Mechanisms, and Stereocontrol
inferred← citeshttps://doi.org/10.1002/slct.201702101openalex-snapshot
Microwave‐Assisted Suzuki‐Miyaura Cross Coupling using Nickel as Catalyst to Rapidly Access to 3‐Arylazetidine
inferred← citeshttps://doi.org/10.1002/slct.202203111openalex-snapshot
Applications of Bond Energy‐Based Thermodynamic Analysis to the Feasibility of Unfunctionalized C−C Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/tcr.202100083openalex-snapshot
(Z)‐Selective Hydrosilylation and Hydroboration of Terminal Alkynes Enabled by Ruthenium Complexes with an N‐Heterocyclic Carbene Ligand
inferred← citeshttps://doi.org/10.1002/zaac.201100162openalex-snapshot
Carbon Halide Bond Activation of Benzyl Chloride and Benzyl Bromide Using An NHC‐Stabilized Nickel(0) Complex
inferred← citeshttps://doi.org/10.1007/128_2011_261openalex-snapshot
Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? A Fruitful Interplay Anyway
inferred← citeshttps://doi.org/10.1007/128_2011_288openalex-snapshot
Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions?: A Fruitful Interplay Anyway
inferred← citeshttps://doi.org/10.1007/978-3-030-65021-6_8openalex-snapshot
Insights into Sustainable C–H Bond Activation
inferred← citeshttps://doi.org/10.1007/978-3-642-32368-3_8openalex-snapshot
Recent Advances in Cross-Coupling Reactions with Alkyl Halides
inferred← citeshttps://doi.org/10.1007/s10562-015-1490-yopenalex-snapshot
Study of the Structure–Activity Relationship in a Heterogeneous Copper–Palladium Catalysed Suzuki–Miyaura Coupling
inferred← citeshttps://doi.org/10.1007/s10593-019-02503-8openalex-snapshot
Piperidines decorated by small (cyclo)alkyl substituents (microreview)
inferred← citeshttps://doi.org/10.1007/s10847-018-0854-5openalex-snapshot
Synthesis of cyclodextrin–pyrrole conjugates possessing tuneable carbon linkers
inferred← citeshttps://doi.org/10.1007/s11164-011-0350-7openalex-snapshot
Ligand-free, PdCl2(PPh3)2 catalyzed, microwave-assisted Suzuki coupling of 1-chloro-3-phenylisoquinoline in the synthesis of diversified 1,3-disubstituted isoquinolines
inferred← citeshttps://doi.org/10.1007/s41061-016-0067-6openalex-snapshot
Ni-Catalyzed C–C Couplings Using Alkyl Electrophiles
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00311-6openalex-snapshot
3.07 Coupling Reactions Between sp3-Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-12-821027-7.00009-8openalex-snapshot
Development of highly regioselective addition reactions of alkenes and alkynes
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00098-9openalex-snapshot
Tricoordinate Carbanions, Cations, and Radicals
inferred← citeshttps://doi.org/10.1016/bs.aihch.2017.10.001openalex-snapshot
Recent Advances in the Synthesis of Piperidines: Functionalization of Preexisting Ring Systems
inferred← citeshttps://doi.org/10.1016/j.catcom.2014.08.010openalex-snapshot
Trans-chloro-(1-naphthyl)bis[tris-(4-methoxyphenyl)phosphane]-nickel(II) catalyzed Suzuki-Miyaura coupling of aryl chlorides with phenylboronic acid
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.04.022openalex-snapshot
Acyclic diaminocarbenes (ADCs) as a promising alternative to N-heterocyclic carbenes (NHCs) in transition metal catalyzed organic transformations
inferred← citeshttps://doi.org/10.1016/j.ccr.2021.214165openalex-snapshot
A new avenue for the preparation of organoboron compounds via nickel catalysis
inferred← citeshttps://doi.org/10.1016/j.ccr.2022.214690openalex-snapshot
Functions of bioinspired pyrrole cobalt complexes–recently developed catalytic systems of vitamin B12 related complexes and porphycene complexes–
inferred← citeshttps://doi.org/10.1016/j.chempr.2017.05.008openalex-snapshot
Recent Developments in Organoboron Chemistry: Old Dogs, New Tricks
inferred← citeshttps://doi.org/10.1016/j.giant.2023.100154openalex-snapshot
Precise control of conjugated polymer synthesis from step-growth polymerization to iterative synthesis
inferred← citeshttps://doi.org/10.1016/j.jcat.2019.03.005openalex-snapshot
A novel zinc-catalyzed Suzuki-type cross-coupling reaction of aryl boronic acids with alkynyl bromides
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2016.02.005openalex-snapshot
Verstile silver(I) and nickel(II) NHC complexes bearing benzotriazole-function: Synthesis, fluorescence and catalytic property
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.120937openalex-snapshot
Synthesis and structural characterization of nickel(II) complexes of 20-membered macrocyclic rings bearing chelating bis(N-heterocyclic carbene) ligands
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123103openalex-snapshot
Evaluation of hemilabile Pd(II) NNS and NNSe non-symmetric pincers in Suzuki–Miyaura cross-coupling: Unexpected selective nitrile hydration of 4-bromonitrobenzene in mild conditions
inferred← citeshttps://doi.org/10.1016/j.jscs.2010.02.011openalex-snapshot
Synthesis of some novel sulfonyl ester derivatives derived from d-mannitol
inferred← citeshttps://doi.org/10.1016/j.molcata.2010.02.021openalex-snapshot
A computational study of phosphine ligand effects in Suzuki–Miyaura coupling☆
inferred← citeshttps://doi.org/10.1016/j.snb.2011.12.034openalex-snapshot
Biosensing invertase-based Langmuir–Schaefer films: Preparation and characteristic
inferred← citeshttps://doi.org/10.1016/j.tet.2011.05.031openalex-snapshot
CuI-catalyzed Suzuki coupling reaction of organoboronic acids with alkynyl bromides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.05.011openalex-snapshot
PdCl2-catalyzed cross-coupling reaction of arylacetylene iodides with arylboronic acids to diarylacetylenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.09.127openalex-snapshot
Silver catalyzed C–C and C–S coupling of aryl halides and thiols with boronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.030openalex-snapshot
Formation of bi-aryls via a domino palladium catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.07.042openalex-snapshot
Nickel catalysed carbonylative Sonogashira reaction for the synthesis of diarylalkynones and 2-substituted flavones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155130openalex-snapshot
A Nickel Catalyzed Suzuki-Miyaura Coupling Reaction of Aryl Halides Facilitated by Pyridine Derivatives
inferred← citeshttps://doi.org/10.1016/j.trechm.2019.08.004openalex-snapshot
Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60217-5openalex-snapshot
Recent advances in mechanistic studies on Ni catalyzed cross-coupling reactions
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00059openalex-snapshot
Metal-Catalyzed Enantioconvergent Transformations
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00162openalex-snapshot
Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C–C Bonds
inferred← citeshttps://doi.org/10.1021/acs.jchemed.0c00478openalex-snapshot
Photochemical Synthesis of Solvatochromic Fluorophore from the C–C Coupling Reaction for Undergraduate Laboratory Experiment
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00665openalex-snapshot
2,6-Bis(pyrazol-1-yl)pyridine (1-bpp) as a General Ligand for the Negishi Alkylation of Alkylpyridinium Salts
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02460openalex-snapshot
Electroreductive C(sp 3 )–C(sp 3 ) Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00806openalex-snapshot
Synthetic Studies toward the Anacolosin Family of Clerodane Diterpene Natural Products
inferred← citeshttps://doi.org/10.1021/acs.jpca.9b04284openalex-snapshot
Mechanism and Origin of Enantioselectivity in Nickel-Catalyzed Alkyl–Alkyl Suzuki Coupling Reaction
inferred← citeshttps://doi.org/10.1021/acs.organomet.2c00032openalex-snapshot
Recent Advances in C(sp3)–C(sp3) Cross-Coupling Chemistry: A Dominant Performance of Nickel Catalysts
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00446openalex-snapshot
Catalysis of Cross-Coupling and Homocoupling Reactions of Aryl Halides Utilizing Ni(0), Ni(I), and Ni(II) Precursors; Ni(0) Compounds as the Probable Catalytic Species but Ni(I) Compounds as Intermediates and Products
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00720openalex-snapshot
Cross-Coupling and Related Reactions: Connecting Past Success to the Development of New Reactions for the Future
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00051openalex-snapshot
Nickel-Catalyzed Negishi Cross-Coupling of Alkyl Halides, Including Unactivated Tertiary Halides, with a Boron-Stabilized Organozinc Reagent
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00567openalex-snapshot
C(sp3)–C(sp3) Coupling of Cycloalkanes and Alkyl Halides via Dual Photocatalytic Hydrogen Atom Transfer and Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03042openalex-snapshot
Direct C–H Allylation of N-Acyl/Sulfonyl Tetrahydroisoquinolines and Analogues
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00283openalex-snapshot
Cp*Rh(III)-Catalyzed Cross-Coupling of Alkyltrifluoroborate with α-Diazomalonates for C(sp3)–C(sp3) Bond Formation
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00793openalex-snapshot
Nickel-Catalyzed Enantioselective Cross-Coupling of N-Hydroxyphthalimide Esters with Vinyl Bromides
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01021openalex-snapshot
Cross-Coupling of Amides with Alkylboranes via Nickel-Catalyzed C–N Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00976openalex-snapshot
Use of the 2-Pyridinesulfonyloxy Leaving Group for the Fast Copper-Catalyzed Coupling Reaction at Secondary Alkyl Carbons with Grignard Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03848openalex-snapshot
Alkyl Halides via Visible Light Mediated Dehalogenation
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04331openalex-snapshot
Cp*Rh(III)-Catalyzed Regioselective C(sp3)–H Methylation of 8-Methylquinolines with Organoborons
inferred← citeshttps://doi.org/10.1021/acscatal.0c03888openalex-snapshot
Switching from Biaryl Formation to Amidation with Convoluted Polymeric Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.1c05586openalex-snapshot
Cobalt-Catalyzed C(sp2)–C(sp3) Suzuki–Miyaura Cross-Coupling Enabled by Well-Defined Precatalysts with L,X-Type Ligands
inferred← citeshttps://doi.org/10.1021/acscatal.2c00933openalex-snapshot
The Catalytic Formation of Atropisomers and Stereocenters via Asymmetric Suzuki–Miyaura Couplings
inferred← citeshttps://doi.org/10.1021/acscatal.2c02433openalex-snapshot
Carboxamide-Directed Stereospecific Couplings of Chiral Tertiary Alkyl Halides with Terminal Alkynes
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.6b00801openalex-snapshot
Nickel-Catalyzed Csp2–Csp3 Cross-Coupling via C–O Bond Activation
inferred← citeshttps://doi.org/10.1021/acscatal.6b03571openalex-snapshot
Copper-Catalyzed Carboxylation of Hydroborated Disubstituted Alkenes and Terminal Alkynes with Cesium Fluoride
inferred← citeshttps://doi.org/10.1021/acscatal.9b03352openalex-snapshot
Nickel/Cobalt-Catalyzed C(sp 3 )–C(sp 3 ) Cross-Coupling of Alkyl Halides with Alkyl Tosylates
inferred← citeshttps://doi.org/10.1021/acscatal.9b03667openalex-snapshot
Suzuki–Miyaura Cross-Coupling of 1,8-Diaminonaphthalene (dan)-Protected Arylboronic Acids
inferred← citeshttps://doi.org/10.1021/acscentsci.5c02173openalex-snapshot
B ‑Alkyl-borabicyclo[3.3.1]nonane Reagents Promote Closed-Shell Nickel-Catalyzed Alkylarylation Toward Encoded Cyclooctene Monomers
inferred← citeshttps://doi.org/10.1021/acscentsci.7b00212openalex-snapshot
Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes
inferred← citeshttps://doi.org/10.1021/cr1002276openalex-snapshot
Transmetalation of Unsaturated Carbon Nucleophiles from Boron-Containing Species to the Mid to Late d-Block Metals of Relevance to Catalytic C−X Coupling Reactions (X = C, F, N, O, Pb, S, Se, Te)
inferred← citeshttps://doi.org/10.1021/cr100327popenalex-snapshot
Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-organometallics as Reaction Partners
inferred← citeshttps://doi.org/10.1021/cs4009946openalex-snapshot
Nickel-Catalyzed Cross-Coupling of Diarylborinic Acids with Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/ja077070ropenalex-snapshot
Palladium-Catalyzed Decarboxylative sp3−sp3 Coupling of Nitrobenzene Acetic Esters
inferred← citeshttps://doi.org/10.1021/ja105176vopenalex-snapshot
Chemoselective and Regiospecific Suzuki Coupling on a Multisubstituted sp 3 -Carbon in 1,1-Diborylalkanes at Room Temperature
inferred← citeshttps://doi.org/10.1021/ja200270kopenalex-snapshot
A Structure–Activity Study of Ni-Catalyzed Alkyl–Alkyl Kumada Coupling. Improved Catalysts for Coupling of Secondary Alkyl Halides
inferred← citeshttps://doi.org/10.1021/ja301612yopenalex-snapshot
New Directing Groups for Metal-Catalyzed Asymmetric Carbon–Carbon Bond-Forming Processes: Stereoconvergent Alkyl–Alkyl Suzuki Cross-Couplings of Unactivated Electrophiles
inferred← citeshttps://doi.org/10.1021/ja304068topenalex-snapshot
Nickel-Catalyzed Coupling Reactions of Alkyl Electrophiles, Including Unactivated Tertiary Halides, To Generate Carbon–Boron Bonds
inferred← citeshttps://doi.org/10.1021/ja504089yopenalex-snapshot
Efficient Synthesis of Secondary Alkyl Fluorides via Suzuki Cross-Coupling Reaction of 1-Halo-1-fluoroalkanes
inferred← citeshttps://doi.org/10.1021/ja8013677openalex-snapshot
Enantioselective Alkyl−Alkyl Suzuki Cross-Couplings of Unactivated Homobenzylic Halides
inferred← citeshttps://doi.org/10.1021/ja910582nopenalex-snapshot
Stereospecific Suzuki Cross-Coupling of Alkyl α-Cyanohydrin Triflates
inferred← citeshttps://doi.org/10.1021/jacs.0c03821openalex-snapshot
Chemoselective Cross-Coupling of gem -Borazirconocene Alkanes with Aryl Halides
inferred← citeshttps://doi.org/10.1021/jacs.1c03563openalex-snapshot
Nickel-Catalyzed Radical Migratory Coupling Enables C-2 Arylation of Carbohydrates
inferred← citeshttps://doi.org/10.1021/jacs.2c02817openalex-snapshot
Copper-Catalyzed Coupling of Alkyl Vicinal Bis(boronic Esters) to an Array of Electrophiles
inferred← citeshttps://doi.org/10.1021/jacs.4c01474openalex-snapshot
(Phenoxyimine)nickel-Catalyzed C(sp 2 )–C(sp 3 ) Suzuki–Miyaura Cross-Coupling: Evidence for a Recovering Radical Chain Mechanism
inferred← citeshttps://doi.org/10.1021/jacs.6b11412openalex-snapshot
Mechanistic Study of an Improved Ni Precatalyst for Suzuki–Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species
inferred← citeshttps://doi.org/10.1021/jacs.6b13389openalex-snapshot
Pd(II)-Catalyzed Enantioselective C(sp3)–H Borylation
inferred← citeshttps://doi.org/10.1021/jacs.6c00526openalex-snapshot
Aminyl Radical-Enabled Photoredox/Nickel-Catalyzed C(sp 3 )–C(sp 3 ) Suzuki–Miyaura Cross-Coupling via Halogen-Atom Transfer Strategy
inferred← citeshttps://doi.org/10.1021/jacs.6c08562openalex-snapshot
Photoelectrocatalysis-Enabled C(sp 3 )–C(sp 3 ) Cross-Coupling of Carboxylic Acids with Alkyl Halides
inferred← citeshttps://doi.org/10.1021/jacs.6c10100openalex-snapshot
Chiral-Ligand-Modulated Nickel-Catalyzed Stereoselective Radical Migratory C2-Arylation of Carbohydrates
inferred← citeshttps://doi.org/10.1021/jacs.6c11534openalex-snapshot
Stereoselective C2′-Alkylation of Nucleosides Enabled by Electrochemical Ni-Catalyzed C(sp3)–C(sp3) Cross-Coupling
inferred← citeshttps://doi.org/10.1021/jacs.7b02389openalex-snapshot
Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C–N Bond Activation
inferred← citeshttps://doi.org/10.1021/jacs.7b10519openalex-snapshot
Ni-Catalyzed Enantioselective Conjunctive Coupling with C(sp3) Electrophiles: A Radical-Ionic Mechanistic Dichotomy
inferred← citeshttps://doi.org/10.1021/jacs.7b12865openalex-snapshot
Ligand-Controlled Chemoselective C(acyl)–O Bond vs C(aryl)–C Bond Activation of Aromatic Esters in Nickel Catalyzed C(sp2)–C(sp3) Cross-Couplings
inferred← citeshttps://doi.org/10.1021/jacs.8b12025openalex-snapshot
Metallaphotoredox-Catalyzed Cross-Electrophile C sp 3 –C sp 3 Coupling of Aliphatic Bromides
inferred← citeshttps://doi.org/10.1021/jo200666zopenalex-snapshot
Palladium(II)-Catalyzed Direct Alkenylation and Arylation of Arenes: Removable 2-Pyridylsulfinyl Group Assisted C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/jo201263ropenalex-snapshot
Stereochemistry of Transmetalation of Alkylboranes in Nickel-Catalyzed Alkyl–Alkyl Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/jo901327yopenalex-snapshot
Mild Room-Temperature Palladium-Catalyzed C3-Arylation of 2(1H)-Pyrazinones via a Desulfitative Kumada-Type Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1021/jo9024754openalex-snapshot
Microwave-Assisted Palladium-Catalyzed Phosphonium Coupling of 2(1H)-Pyrazinones
inferred← citeshttps://doi.org/10.1021/jp7121517openalex-snapshot
Pd Nanoparticles Immobilized on pH-Responsive and Chelating Nanospheres as an Efficient and Recyclable Catalyst for Suzuki Reaction in Water
inferred← citeshttps://doi.org/10.1021/ol101995vopenalex-snapshot
Rhodium-Catalyzed Activation of C(sp 3 )−X (X = Cl, Br) Bond: An Intermolecular Halogen Exchange Case
inferred← citeshttps://doi.org/10.1021/ol3006997openalex-snapshot
Palladium-Catalyzed C–H Alkenylation of Arenes Using Thioethers as Directing Groups
inferred← citeshttps://doi.org/10.1021/ol302067bopenalex-snapshot
Nickel-Catalyzed Diastereoselective Alkyl–Alkyl Kumada Coupling Reactions
inferred← citeshttps://doi.org/10.1021/ol302106yopenalex-snapshot
Enantioselective Total Synthesis of (−)-Laurenditerpenol
inferred← citeshttps://doi.org/10.1021/ol500057aopenalex-snapshot
Development of the Direct Suzuki–Miyaura Cross-Coupling of Primary B-Alkyl MIDA-boronates and Aryl Bromides
showing the first 200 of 263 · page through all 263
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.