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Tetrahydroxydiboron-Mediated Palladium-Catalyzed Transfer Hydrogenation and Deuteriation of Alkenes and Alkynes Using Water as the Stoichiometric H or D Atom Donor
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Mild and General Access to Diverse 1H‐Benzotriazoles via Diboron‐Mediated NOH Deoxygenation and Palladium‐ Catalyzed CC and CN Bond Formation
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The Renaissance of H/D Exchange
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Palladium‐Catalyzed Direct Synthesis of Organoboronic Acids
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Palladium‐Catalyzed Synthesis and Isolation of Functionalized Allylboronic Acids: Selective, Direct Allylboration of Ketones
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Scope and Selectivity of Heterogeneous Rh0‐Catalyzed Tandem Dehydrocoupling/Hydrogenation Using Me2NH·BH3 as a Stoichiometric H2 Source
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Pd‐Catalyzed Hydrogen‐Transfer Reactions from Alcohols to C=C, C=O, and C=N Bonds
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Catalytic hydrogenation for the industrial synthesis of the Wong’s anthracyclines intermediate
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Nickel-catalyzed (E)-selective semihydrogenation of internal alkynes with hypophosphorous acid
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A modified procedure for the palladium catalyzed borylation/Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides utilizing bis-boronic acid
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Hydrogenation of alkenes or alkynes using decaborane in methanol
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Chapter 25 The Use of Isotopically Labeled Compounds in Drug Discovery
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A review of the problem of distinguishing true homogeneous catalysis from soluble or other metal-particle heterogeneous catalysis under reducing conditions
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The Golden Age of Transfer Hydrogenation
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Development, Mechanism, and Scope of the Palladium-Catalyzed Enantioselective Allene Diboration
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Ruthenium-Catalyzed Selective α,β-Deuteration of Bioactive Amines
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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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inferred← citeshttps://doi.org/10.1002/anie.202214433openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.3c01773openalex-snapshot
The Proton of Alcohols as Hydrogen Source in Diboron-Mediated Nickel-Catalyzed Asymmetric Transfer Hydrogenation of Cyclic N-Sulfonyl Imines
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01425openalex-snapshot
Tetrahydroxydiboron-Mediated Synthesis of α-Sulfonyl Ketoximes from Nitroalkenes and Sodium Sulfinates
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02134openalex-snapshot
Synthesis of C2-Alkyl Quinazolinones through Bis(pinacolato)diborane Mediated Transfer Hydrogenation Reaction of Alkynes to Alkanes
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00580openalex-snapshot
Pd-Boron-Catalyzed One Carbon Isomerization of Olefins: Water Assisted Process at Room Temperature
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01965openalex-snapshot
Employing Water as the Hydride Source in Synthesis: A Case Study of Diboron Mediated Alkyne Hydroarylation
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00321openalex-snapshot
Diboron-Assisted Copper-Catalyzed Z-Selective Semihydrogenation of Alkynes Using Ethanol as a Hydrogen Donor
inferred← citeshttps://doi.org/10.1021/acs.oprd.1c00198openalex-snapshot
Hydrogen Evolution from Telescoped Miyaura Borylation and Suzuki Couplings Utilizing Diboron Reagents: Process Safety and Hazard Considerations
inferred← citeshttps://doi.org/10.1021/acs.organomet.0c00413openalex-snapshot
An Annelated Mesoionic Carbene (MIC) Based Ru(II) Catalyst for Chemo- and Stereoselective Semihydrogenation of Internal and Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00286openalex-snapshot
Heterogenization of Trinuclear Palladium Complex into an Anionic Metal–Organic Framework through Postsynthetic Cation Exchange
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00112openalex-snapshot
Asymmetric Umpolung Hydrogenation and Deuteration of Alkenes Catalyzed by Nickel
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02367openalex-snapshot
Tetrahydroxydiboron-Promoted Radical Addition of Alkynols
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03632openalex-snapshot
Copper-Catalyzed Formal Transfer Hydrogenation/Deuteration of Aryl Alkynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00341openalex-snapshot
Mild and Selective Rhodium-Catalyzed Transfer Hydrogenation of Functionalized Arenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01095openalex-snapshot
Hydrogen-Bonding Controlled Nickel-Catalyzed Regioselective Cyclotrimerization of Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01082openalex-snapshot
Enantioselective Palladium-Catalyzed Arylborylation/Cyclization of Alkenes to Access Boryl-Functionalized Heterocyclic Compounds Containing Quaternary Stereogenic Centers
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03664openalex-snapshot
Mild and Selective Hydrogenation of Unsaturated Compounds Using Mn/Water as a Hydrogen Gas Source
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01999openalex-snapshot
Diboron-Assisted Palladium-Catalyzed Transfer Hydrogenation of N-Heteroaromatics with Water as Hydrogen Donor and Solvent
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02508openalex-snapshot
Generation of Hydrogen from Water: A Pd-Catalyzed Reduction of Water Using Diboron Reagent at Ambient Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01036openalex-snapshot
Pd-Catalyzed Regioselective 1,2-Difunctionalization of Vinylarenes with Alkenyl Triflates and Aryl Boronic Acids at Ambient Temperature
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01208openalex-snapshot
Regioselective Ni-Catalyzed Carboxylation of Allylic and Propargylic Alcohols with Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02701openalex-snapshot
B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01806openalex-snapshot
B2pin2-Mediated Palladium-Catalyzed Diacetoxylation of Aryl Alkenes with O2 as Oxygen Source and Sole Oxidant
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02244openalex-snapshot
Transition-Metal-Free Highly Chemoselective and Stereoselective Reduction with Se/DMF/H2O System
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00059openalex-snapshot
Asymmetric Transfer Hydrogenation of Heterobicyclic Alkenes with Water as Hydrogen Source
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00148openalex-snapshot
Water as a Hydrogenating Agent: Stereodivergent Pd-Catalyzed Semihydrogenation of Alkynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00497openalex-snapshot
A Mild, DNA-Compatible Nitro Reduction Using B2(OH)4
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02287openalex-snapshot
Cascade Alkynylation and Highly Selective Hydrogenation Catalyzed by Binaphthyl-Palladium Nanoparticles Accessing Phosphinyl (Z)-[3]Dendralenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02369openalex-snapshot
Ag2CO3-Catalyzed H/D Exchange of Five-Membered Heteroarenes at Ambient Temperature
inferred← citeshttps://doi.org/10.1021/acsaem.2c00286openalex-snapshot
Sharp Volcano-Type Synergy and Visible Light Acceleration in H 2 Release upon B 2 (OH) 4 Hydrolysis Catalyzed by Au-Rh@Click-Dendrimer Nanozymes
inferred← citeshttps://doi.org/10.1021/acsami.0c14486openalex-snapshot
The Immobilization of Pd(II) on Porous Organic Polymers for Semihydrogenation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acsanm.4c01521openalex-snapshot
Pd Nanoparticles Supported on N-Doped Porous Carbon Cathodes for the Catalytic Semideuteration of Alkynes
inferred← citeshttps://doi.org/10.1021/acscatal.1c01000openalex-snapshot
Reductive Activation and Hydrofunctionalization of Olefins by Multiphoton Tandem Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.3c00326openalex-snapshot
Photocatalytic Transfer Hydrogenation Reactions Using Water as the Proton Source
inferred← citeshttps://doi.org/10.1021/acscatal.3c05928openalex-snapshot
Promoting Electrocatalytic Semihydrogenation of Alkynols to Alkenols over a Bimetallic CuAu Alloy Catalyst
inferred← citeshttps://doi.org/10.1021/acscatal.5c03926openalex-snapshot
Palladium-Catalyzed Aerobic Alkene Arylboration: Coupling Aryl Boronic Acids, Alkenes, and Bis(pinacol)diboron
inferred← citeshttps://doi.org/10.1021/acscatal.7b01043openalex-snapshot
Visible-Light-Driven Self-Hydrogen Transfer Hydrogenolysis of Lignin Models and Extracts into Phenolic Products
inferred← citeshttps://doi.org/10.1021/acscatal.9b00761openalex-snapshot
Selective Dehydrogenative Mono- or Diborylation of Styrenes by Supported Copper Catalysts
inferred← citeshttps://doi.org/10.1021/acscatal.9b03172openalex-snapshot
Nickel-Catalyzed Enantioselective Reductive Aryl Fluoroalkenylation of Alkenes
inferred← citeshttps://doi.org/10.1021/acsmaterialslett.2c01046openalex-snapshot
A Deeper Understanding of H 2 Evolution Entirely from Water via Diborane Hydrolysis
inferred← citeshttps://doi.org/10.1021/acsomega.3c07550openalex-snapshot
Facile Transfer Hydrogenation of N-Heteroarenes and Nitroarenes Using Magnetically Recoverable Pd@SPIONs Catalyst
inferred← citeshttps://doi.org/10.1021/acsomega.9b03328openalex-snapshot
B(C6F5)3-Catalyzed C–C Coupling of 1,4-Naphthoquinones with the C-3 Position of Indole Derivatives in Water
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c02496openalex-snapshot
Catalyzed Hydrolysis of Tetrahydroxydiboron by Graphene Quantum Dot-Stabilized Transition-Metal Nanoparticles for Hydrogen Evolution
inferred← citeshttps://doi.org/10.1021/acssuschemeng.1c00633openalex-snapshot
Transfer Hydrogenation of Aldehydes and Ketones in Air with Methanol and Ethanol by an Air-Stable Ruthenium–Triazole Complex
inferred← citeshttps://doi.org/10.1021/acssuschemeng.3c01104openalex-snapshot
Base-Free Transfer Hydrogenation Catalyzed by Ruthenium Hydride Complexes of Coumarin-Amide Ligands
inferred← citeshttps://doi.org/10.1021/jacs.7b02581openalex-snapshot
Remarkably Facile Borane-Promoted, Rhodium-Catalyzed Asymmetric Hydrogenation of Tri- and Tetrasubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.7b07637openalex-snapshot
Site-Selective Catalytic Carboxylation of Unsaturated Hydrocarbons with CO2 and Water
inferred← citeshttps://doi.org/10.1021/jacs.7b09832openalex-snapshot
Cobalt-Catalyzed Asymmetric Sequential Hydroboration/Hydrogenation of Internal Alkynes
inferred← citeshttps://doi.org/10.1021/jacs.7b13220openalex-snapshot
Ni-Catalyzed Site-Selective Dicarboxylation of 1,3-Dienes with CO2
inferred← citeshttps://doi.org/10.1021/jacs.8b01038openalex-snapshot
Transfer Hydrogenation of Alkenes Using Ethanol Catalyzed by a NCP Pincer Iridium Complex: Scope and Mechanism
inferred← citeshttps://doi.org/10.1038/s41467-021-23971-7openalex-snapshot
C(sp3)−C(sp3) bond formation via nickel-catalyzed deoxygenative homo-coupling of aldehydes/ketones mediated by hydrazine
inferred← citeshttps://doi.org/10.1038/s41467-021-25229-8openalex-snapshot
Direct deoxygenative borylation of carboxylic acids
inferred← citeshttps://doi.org/10.1038/s41467-023-36378-3openalex-snapshot
Tripodal Pd metallenes mediated by Nb2C MXenes for boosting alkynes semihydrogenation
inferred← citeshttps://doi.org/10.1038/s41467-023-37022-wopenalex-snapshot
Modulation of metal species as control point for Ni-catalyzed stereodivergent semihydrogenation of alkynes with water
inferred← citeshttps://doi.org/10.1038/s41467-023-40138-8openalex-snapshot
Diversity-oriented synthesis of P-stereogenic and axially chiral monodentate biaryl phosphines enabled by C-P bond cleavage
inferred← citeshttps://doi.org/10.1038/s41467-025-57782-xopenalex-snapshot
Electrochemical cobalt-catalyzed semi-deuteration of alkynes to access deuterated Z-alkenes
inferred← citeshttps://doi.org/10.1038/s41467-025-57855-xopenalex-snapshot
Pd-catalyzed deuteration of aryl halides with deuterium oxide
inferred← citeshttps://doi.org/10.1038/s41467-025-67482-1openalex-snapshot
Decatungstate-photocatalyzed transfer hydrogenation of unsaturated compounds using alcohol as the hydrogen source
inferred← citeshttps://doi.org/10.1038/s41596-025-01230-zopenalex-snapshot
Electrocatalytic semi-hydrogenation of alkynes using water as the hydrogen source
inferred← citeshttps://doi.org/10.1038/s41598-021-88528-6openalex-snapshot
A magnetically retrievable mixed-valent Fe3O4@SiO2/Pd0/PdII nanocomposite exhibiting facile tandem Suzuki coupling/transfer hydrogenation reaction
inferred← citeshttps://doi.org/10.1038/s41929-020-0470-9openalex-snapshot
Site-selective alkene borylation enabled by synergistic hydrometallation and borometallation
inferred← citeshttps://doi.org/10.1038/s41929-024-01286-2openalex-snapshot
A hydrogenative oxidation strategy for the single-step synthesis of lactams from N-heteroarenes using water
inferred← citeshttps://doi.org/10.1038/s44160-024-00537-1openalex-snapshot
Aluminium(I) anion-supported zero-valent palladium complexes
inferred← citeshttps://doi.org/10.1039/c7cc09432aopenalex-snapshot
Palladium-catalyzed regioselective hydroboration of aryl alkenes with B 2 pin 2
inferred← citeshttps://doi.org/10.1039/c7cy00231aopenalex-snapshot
N/O-doped carbon as a “solid ligand” for nano-Pd catalyzed biphenyl- and triphenylamine syntheses
inferred← citeshttps://doi.org/10.1039/c7ob00762kopenalex-snapshot
Pd(0)-Catalysed asymmetric reductive Heck-type cyclization of (Z)-1-iodo-1,6-dienes and enantioselective synthesis of quaternary tetrahydropyridines
inferred← citeshttps://doi.org/10.1039/c7ob00820aopenalex-snapshot
Umpolung of protons from H 2 O: a metal-free chemoselective reduction of carbonyl compounds via B 2 pin 2 /H 2 O systems
inferred← citeshttps://doi.org/10.1039/c7qo00604gopenalex-snapshot
B 2 (OH) 4 -mediated one-pot synthesis of tetrahydroquinoxalines from 2-amino(nitro)anilines and 1,2-dicarbonyl compounds in water
inferred← citeshttps://doi.org/10.1039/c7qo00769hopenalex-snapshot
An expedient and novel strategy for reductive amination by employing H 2 O as both a hydrogen source and solvent via B 2 (OH) 4 /H 2 O systems
inferred← citeshttps://doi.org/10.1039/c8dt02168fopenalex-snapshot
Hydrodebromination of allylic and benzylic bromides with water catalyzed by a rhodium porphyrin complex
inferred← citeshttps://doi.org/10.1039/c8qo00942bopenalex-snapshot
Reductive N -alkylation of primary and secondary amines using carboxylic acids and borazane under mild conditions
inferred← citeshttps://doi.org/10.1039/c9cc00797kopenalex-snapshot
A palladium-catalyzed regiocontrollable hydroarylation reaction of allenamides with B 2 pin 2 /H 2 O
inferred← citeshttps://doi.org/10.1039/c9cc03213dopenalex-snapshot
Copper-catalysed, diboron-mediated cis -dideuterated semihydrogenation of alkynes with heavy water
inferred← citeshttps://doi.org/10.1039/c9cc04011kopenalex-snapshot
Cu-Catalyzed highly selective reductive functionalization of 1,3-diene using H 2 O as a stoichiometric hydrogen atom donor
inferred← citeshttps://doi.org/10.1039/c9ob02095kopenalex-snapshot
Rhodium-catalyzed transfer hydrogenation of quinoxalines with water as a hydrogen source
inferred← citeshttps://doi.org/10.1039/c9qo00007kopenalex-snapshot
Cooperation between an alcoholic proton and boryl species in the catalytic gem -hydrodiborylation of carboxylic esters to access 1,1-diborylalkanes
inferred← citeshttps://doi.org/10.1039/c9qo00231fopenalex-snapshot
Photocatalyzed transfer hydrogenation and deuteriation of cyclic N -sulfonylimines
inferred← citeshttps://doi.org/10.1039/c9qo00616hopenalex-snapshot
Ligandless nickel-catalyzed transfer hydrogenation of alkenes and alkynes using water as the hydrogen donor
inferred← citeshttps://doi.org/10.1039/c9ra06285hopenalex-snapshot
Pd nanoparticles on green support as dip-catalyst: a facile transfer hydrogenation of olefins and N -heteroarenes in water
inferred← citeshttps://doi.org/10.1039/d0cc02146fopenalex-snapshot
Triflyl-assisted reductive Pd-catalyzed Tsuji–Trost type reaction
inferred← citeshttps://doi.org/10.1039/d0cy01442gopenalex-snapshot
Pd catalysts supported on dual-pore monolithic silica beads for chemoselective hydrogenation under batch and flow reaction conditions
inferred← citeshttps://doi.org/10.1039/d0ob02080jopenalex-snapshot
Pd/C-Catalyzed transfer hydrogenation of N –H indoles with trifluoroethanol and tetrahydroxydiboron as the hydrogen source
inferred← citeshttps://doi.org/10.1039/d0qo00468eopenalex-snapshot
Copper-catalyzed mild desulfonylation of vinyl sulfonyl molecules
inferred← citeshttps://doi.org/10.1039/d1cp05277bopenalex-snapshot
Mechanistic insights into H 2 evolution via water splitting at the expense of B 2 (OH) 4 : a theoretical study
inferred← citeshttps://doi.org/10.1039/d1ob00155hopenalex-snapshot
Zinc salt-catalyzed reduction of α-aryl imino esters, diketones and phenylacetylenes with water as hydrogen source
inferred← citeshttps://doi.org/10.1039/d1ob00300copenalex-snapshot
Metal-free reduction of unsaturated carbonyls, quinones, and pyridinium salts with tetrahydroxydiboron/water
inferred← citeshttps://doi.org/10.1039/d1qo00581bopenalex-snapshot
Palladium-catalyzed divergent cycloisomerization of 1,6-enynes controlled by functional groups for the synthesis of pyrroles, cyclopentenes, and tetrahydropyridines
inferred← citeshttps://doi.org/10.1039/d2gc04315gopenalex-snapshot
Catalyst-free transfer hydrogenation of activated alkenes exploiting isopropanol as the sole and traceless reductant
inferred← citeshttps://doi.org/10.1039/d2qi01313dopenalex-snapshot
Cobalt sandwich-stabilized rhodium nanocatalysts for ammonia borane and tetrahydroxydiboron hydrolysis
inferred← citeshttps://doi.org/10.1039/d2sc03590aopenalex-snapshot
A switchable redox annulation of 2-nitroarylethanols affording N -heterocycles: photoexcited nitro as a multifunctional handle
inferred← citeshttps://doi.org/10.1039/d3gc03290fopenalex-snapshot
CO 2 promoted photoredox/Ni-catalyzed semi-reduction of alkynes with H 2 O
inferred← citeshttps://doi.org/10.1039/d3gc04699kopenalex-snapshot
TfOH-catalyzed transfer hydrogenation reaction using 1-tetralone as a novel dihydrogen source
inferred← citeshttps://doi.org/10.1039/d3ob00705gopenalex-snapshot
Highly stereoselective synthesis of trans -alkenes via electrochemical Ni-catalyzed hydroarylation of alkynes with aryl iodides
inferred← citeshttps://doi.org/10.1039/d4gc05928jopenalex-snapshot
Nickel-catalyzed transfer hydrogenative cross-coupling of nitriles and amines with B 2 (OH) 4 /H 2 O system
inferred← citeshttps://doi.org/10.1039/d4ob01958jopenalex-snapshot
Chemo- and stereoselective synthesis of Z -alkenes via electrochemical Pd-catalyzed alkyne reduction
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