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Novel Palladium(0)-Catalyzed Coupling Reaction of Dialkoxyborane with Aryl Halides: Convenient Synthetic Route to Arylboronates
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Catalytic Hydroboration with Rhodium Complexes
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Organoborane Chemistry
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Reaction of ethyl haloacetates and .alpha.-bromo ketones with B-aryl-9-borabicyclo(3.3.1)nonanes under the influence of potassium tert-butoxide. A new convenient procedure for the .alpha.-arylation of ketones and esters
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Palladium(0)-Catalyzed Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters
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Hydroboration of Olefins with Catecholborane at Room Temperature in the Presence of N,N-Dimethylacetamide
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Versatile Method for the Synthesis of Iodosilanes
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PdCl2-Catalyzed Reduction of Organic Halides by Triethylsilane
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1002/anie.200905824openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.11.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2014.04.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2004.04.057openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2006.02.068openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2007.02.103openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2008.02.111openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2008.03.102openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.065openalex-snapshot
Lithium aminoborohydrides 17. Palladium catalyzed borylation of aryl iodides, bromides, and triflates with diisopropylaminoborane prepared from lithium diisopropylaminoborohydride
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.057openalex-snapshot
Suzuki–Miyaura cross-coupling reaction of aryl and heteroaryl pinacol boronates for the synthesis of 2-substituted pyrimidines
inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.016openalex-snapshot
Halodeboronation of organotrifluoroborates using tetrabutylammonium tribromide or cesium triiodide
inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.033openalex-snapshot
Ag(I)-catalyzed C–H borylation of terminal alkynes
inferred← citeshttps://doi.org/10.1016/j.tet.2018.12.040openalex-snapshot
Organoboron chemistry comes to light: Recent advances in photoinduced synthetic approaches to organoboron compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.10.063openalex-snapshot
Microwave-assisted functionalization of bromo-fluorescein and bromorhodamine derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.04.129openalex-snapshot
A facile and convenient synthesis of functionalized ortho-nitrophenylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.02.093openalex-snapshot
Investigation of the asymmetric Birch reduction–alkylation of a chiral 5-arylbenzamide containing a carbamate group
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.064openalex-snapshot
First synthesis of bidentate NHC–Pd complexes with anthracene and xanthene skeletons
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.11.035openalex-snapshot
Phthalocyanine-boronates: a synthon for the preparation of molecular assemblies
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.01.006openalex-snapshot
Palladium-catalyzed borylation of l-tyrosine triflate derivative with pinacolborane: practical route to 4-borono-l-phenylalanine (l-BPA) derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.007openalex-snapshot
Metal free ipso iodination0 of arylboronic acids using CTAB/I2 in aqueous media: green and regioselective synthesis of aryliodides under mild conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153478openalex-snapshot
Synthesis of arylboronates via the Pd-catalyzed desulfitative coupling reaction of sodium arylsulfinates with bis(pinacolato)diboron
inferred← citeshttps://doi.org/10.1016/s0010-8545(98)00138-6openalex-snapshot
Transition metals in organic synthesis, highlights for the year 1997
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00998-xopenalex-snapshot
Synthesis of pinacol arylboronates via cross-coupling reaction of bis(pinacolato)diboron with chloroarenes catalyzed by palladium(0)–tricyclohexylphosphine complexes
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00076-5openalex-snapshot
Palladium-catalysed reactions of aryl halides with soft, non-organometallic nucleophiles
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00616-1openalex-snapshot
Stereoselective access to functionalized β-γ unsaturated acids
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)00881-9openalex-snapshot
Regio- and stereoselective synthesis of allylboranes via platinum(0)-catalyzed borylation of allyl halides with pinacolborane
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01076-5openalex-snapshot
Palladium-catalyzed cross-coupling of aryldiazonium tetrafluoroborate salts with arylboronic esters
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01573-2openalex-snapshot
Palladium-catalyzed borylation of aryldiazonium tetrafluoroborate salts. A new synthesis of arylboronic esters
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01619-1openalex-snapshot
Stereospecific synthesis of functional alkenylsilanes via silastannation of but-3-ynoic acid
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01848-2openalex-snapshot
First synthesis and electronic properties of (hetero)aryl bridged and directly linked redox active phenothiazinyl dyads and triads
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00980-8openalex-snapshot
Palladium-catalyzed cross-coupling reaction of allyl acetates with pinacol aryl- and vinylboronates
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02272-2openalex-snapshot
Enantioselective synthesis of 4-substituted phenylalanines by cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00253-1openalex-snapshot
Rhodium-catalyzed dehydrogenative coupling reaction of vinylarenes with pinacolborane to vinylboronates
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)01793-1openalex-snapshot
Synthesis of alkenylsilanes via palladium(0)-catalyzed silylation of alkenyl iodides with hydrosilane
inferred← citeshttps://doi.org/10.1016/s0169-3158(06)80002-2openalex-snapshot
Chemistry of the diboron compounds
inferred← citeshttps://doi.org/10.1016/s0960-894x(00)00601-6openalex-snapshot
Inhibition of RANTES/CCR1-mediated chemotaxis by cosalane and related compounds
inferred← citeshttps://doi.org/10.1016/s0969-8051(02)00344-xopenalex-snapshot
Synthesis of radioiodinated aryl iodides via boronate precursors
inferred← citeshttps://doi.org/10.1016/s1045-0688(98)80007-5openalex-snapshot
Synthesis of biaryls via the cross-coupling reaction of arylboronic acids
inferred← citeshttps://doi.org/10.1016/s1460-1567(00)80009-4openalex-snapshot
Chapter 5 Thiophenes and benzo[b]thiophenes
inferred← citeshttps://doi.org/10.1016/s1460-1567(07)80054-7openalex-snapshot
Chapter 5 Thiophenes and benzo[b]thiophenes
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00417openalex-snapshot
Inorganometallics (Transition Metal–Metalloid Complexes) and Catalysis
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c02337openalex-snapshot
Conversion of Carbon Dioxide into a Series of CBxOy– Compounds Mediated by LaB3,4O2– Anions: Synergy of the Electron Transfer and Lewis Pair Mechanisms to Construct B–C Bonds
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c02602openalex-snapshot
Phenotypic Hit Identification and Optimization of Novel Pan-TEAD and Subtype-Selective Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01252openalex-snapshot
Late-Stage Functionalization of the Periphery of Oligophenylene Dendrimers with Various Arene Units via Fourfold C–H Borylation
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01721openalex-snapshot
A Bicyclic N-Heterocyclic Carbene as a Bulky but Accessible Ligand: Application to the Copper-Catalyzed Borylations of Aryl Halides
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00469openalex-snapshot
Visible-Light-Mediated Borylation of Arenes via an Electron Donor–Acceptor Complex of Thianthrenium Salts
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01467openalex-snapshot
Functional Group Compatibility of the Oxidation-Resistant Benzoxaborolone Pharmacophore
inferred← citeshttps://doi.org/10.1021/acs.joc.7b03009openalex-snapshot
Scalable 9-Step Synthesis of the Splicing Modulator NVS-SM2
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01662openalex-snapshot
Additive- and Photocatalyst-Free Borylation of Arylazo Sulfones under Visible Light
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00350openalex-snapshot
Functionalization of Deutero- and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.oprd.6b00345openalex-snapshot
Development and Scale-up of an Efficient Miyaura Borylation Process Using Tetrahydroxydiboron
inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00968openalex-snapshot
Intramolecular Hydride Transfer Reactions in (Formazanate)Boron Dihydride Complexes
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00161openalex-snapshot
Cobalt-Catalyzed Borylation of Aryl Halides and Pseudohalides
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00899openalex-snapshot
Cyclo[9]pyrrole: Selective Synthesis of [34]Nonaphyrin(0.0.0.0.0.0.0.0.0)
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01768openalex-snapshot
Stereoselective Synthesis of Difluorinated 1,3-Dienes via Palladium-Catalyzed C–F Bond Activation of Tetrasubstituted gem-Difluoroalkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00976openalex-snapshot
Dearomatization of Heteroarenium Salts with ArBpin Reagents. Application to the Total Synthesis of a Nuphar Alkaloid
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04643openalex-snapshot
Radical Borylation of Aryl Sulfones with N -Heterocyclic Carbene Borane: A Modular Approach to Aryl Boranes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03621openalex-snapshot
Pd(0)-Catalyzed Cyclizative Carboboration of n-Iodo-1,6-diene (n = 1 or 2): Access to Structurally Complex Allylboronates and Alkylboronates
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03850openalex-snapshot
Redox-Neutral Borylation of Aryl Sulfonium Salts via C–S Activation Enabled by Light
inferred← citeshttps://doi.org/10.1021/acscatal.4c04576openalex-snapshot
Pd-Catalyzed B–H Aryl/Alkenylation of 1,2-Azaborines
inferred← citeshttps://doi.org/10.1021/acscentsci.0c01300openalex-snapshot
Pd-Catalyzed Cross Coupling Strategy for Functional Porphyrin Arrays
inferred← citeshttps://doi.org/10.1021/acsinfecdis.3c00657openalex-snapshot
Synthesis of Bisindole Alkaloids and Their Mode of Action against Methicillin-Resistant Staphylococcus Aureus
inferred← citeshttps://doi.org/10.1021/cr000664ropenalex-snapshot
Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
inferred← citeshttps://doi.org/10.1021/ic3026655openalex-snapshot
Design of Triads for Probing the Direct Through Space Energy Transfers in Closely Spaced Assemblies
inferred← citeshttps://doi.org/10.1021/ja0202255openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reaction of Bis(pinacolato)diboron with 1-Alkenyl Halides or Triflates: Convenient Synthesis of Unsymmetrical 1,3-Dienes via the Borylation-Coupling Sequence
inferred← citeshttps://doi.org/10.1021/ja028518lopenalex-snapshot
Catalyzed Asymmetric Aryl Transfer Reactions to Aldehydes with Boronic Acids as Aryl Source
inferred← citeshttps://doi.org/10.1021/ja053433gopenalex-snapshot
Mechanism of the Mild Functionalization of Arenes by Diboron Reagents Catalyzed by Iridium Complexes. Intermediacy and Chemistry of Bipyridine-Ligated Iridium Trisboryl Complexes
inferred← citeshttps://doi.org/10.1021/ja1052973openalex-snapshot
An Opportunity for Mg-Catalyzed Grignard-Type Reactions: Direct Coupling of Benzylic Halides with Pinacolborane with 10 mol % of Magnesium
inferred← citeshttps://doi.org/10.1021/ja2097095openalex-snapshot
Pd-Catalyzed Oxidative ortho -C–H Borylation of Arenes
inferred← citeshttps://doi.org/10.1021/ja8055886openalex-snapshot
Axially Chiral β,β′-Bisporphyrins: Synthesis and Configurational Stability Tuned by the Central Metals
inferred← citeshttps://doi.org/10.1021/ja901095hopenalex-snapshot
Synthesis of 1-Borylisoindoles via Palladium-Catalyzed Dehydrogenation/C−H Borylation of Isoindolines
inferred← citeshttps://doi.org/10.1021/ja910808xopenalex-snapshot
Neopentylglycolborylation of Aryl Mesylates and Tosylates Catalyzed by Ni-Based Mixed-Ligand Systems Activated with Zn
inferred← citeshttps://doi.org/10.1021/jacs.6b01376openalex-snapshot
Scalable, Metal- and Additive-Free, Photoinduced Borylation of Haloarenes and Quaternary Arylammonium Salts
inferred← citeshttps://doi.org/10.1021/jacs.9b13019openalex-snapshot
Axially Chiral Spiro-Conjugated Carbon-Bridged p-Phenylenevinylene Congeners: Synthetic Design and Materials Properties
inferred← citeshttps://doi.org/10.1021/jo005663dopenalex-snapshot
Palladium-Catalyzed Borylation of Ortho-Substituted Phenyl Halides and Application to the One-Pot Synthesis of 2,2‘-Disubstituted Biphenyls
inferred← citeshttps://doi.org/10.1021/jo010098fopenalex-snapshot
Synthesis of Novel Quinone Boronic Ester Derivatives via a Highly Regioselective Cr-Mediated Benzannulation Reaction and Their Application in Pd-Catalyzed Coupling Processes
inferred← citeshttps://doi.org/10.1021/jo010747nopenalex-snapshot
Rhodium(I)-Catalyzed Asymmetric 1,4-Addition of Arylboronic Acids to α,β-Unsaturated Amides
inferred← citeshttps://doi.org/10.1021/jo0160726openalex-snapshot
Application of the Palladium-Catalyzed Borylation/Suzuki Coupling (BSC) Reaction to the Synthesis of Biologically Active Biaryl Lactams
inferred← citeshttps://doi.org/10.1021/jo0269114openalex-snapshot
An Improved Preparation of Arylboronates: Application in One-Pot Suzuki Biaryl Synthesis†
inferred← citeshttps://doi.org/10.1021/jo0491612openalex-snapshot
Arylboronic Acids and Arylpinacolboronate Esters in Suzuki Coupling Reactions Involving Indoles. Partner Role Swapping and Heterocycle Protection
inferred← citeshttps://doi.org/10.1021/jo050995+openalex-snapshot
Preparation and Suzuki−Miyaura Coupling Reactions of Tetrahydropyridine-2-boronic Acid Pinacol Esters
inferred← citeshttps://doi.org/10.1021/jo052400gopenalex-snapshot
Synthesis of Substituted 2-Cyanoarylboronic Esters
inferred← citeshttps://doi.org/10.1021/jo060729bopenalex-snapshot
Comparative Study of the Kumada, Negishi, Stille, and Suzuki−Miyaura Reactions in the Synthesis of the Indole Alkaloids Hippadine and Pratosine
inferred← citeshttps://doi.org/10.1021/jo062627ropenalex-snapshot
Oxidative Rearrangement of Indoles: A New Approach to the EFHG-Tetracyclic Core of Diazonamide A
inferred← citeshttps://doi.org/10.1021/jo1004907openalex-snapshot
Ambient-Temperature Cobalt-Catalyzed Cycloaddition Strategies to Aromatic Boronic Esters
inferred← citeshttps://doi.org/10.1021/jo101023topenalex-snapshot
Neopentylglycolborylation of ortho-Substituted Aryl Halides Catalyzed by NiCl2-Based Mixed-Ligand Systems
inferred← citeshttps://doi.org/10.1021/jo101718vopenalex-snapshot
Zero-Valent Metals Accelerate the Neopentylglycolborylation of Aryl Halides Catalyzed by NiCl 2 -Based Mixed-Ligand Systems
inferred← citeshttps://doi.org/10.1021/jo201093uopenalex-snapshot
Hydride as a Leaving Group in the Reaction of Pinacolborane with Halides under Ambient Grignard and Barbier Conditions. One-Pot Synthesis of Alkyl, Aryl, Heteroaryl, Vinyl, and Allyl Pinacolboronic Esters
inferred← citeshttps://doi.org/10.1021/jo202037xopenalex-snapshot
Ni(COD)2/PCy3 Catalyzed Cross-Coupling of Aryl and Heteroaryl Neopentylglycolboronates with Aryl and Heteroaryl Mesylates and Sulfamates in THF at Room Temperature
inferred← citeshttps://doi.org/10.1021/jo3018878openalex-snapshot
Synthesis of Pinacol Arylboronates from Aromatic Amines: A Metal-Free Transformation
inferred← citeshttps://doi.org/10.1021/jo400469topenalex-snapshot
Stereospecific Approach to the Synthesis of Ring-A Oxygenated Sarpagine Indole Alkaloids. Total Synthesis of the Dimeric Indole Alkaloid P-(+)-Dispegatrine and Six Other Monomeric Indole Alkaloids
inferred← citeshttps://doi.org/10.1021/jo401104yopenalex-snapshot
Nickel-Catalyzed Borylation of Halides and Pseudohalides with Tetrahydroxydiboron [B 2 (OH) 4 ]
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