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Triflyl-assisted reductive Pd-catalyzed Tsuji–Trost type reaction
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.201700195openalex-snapshot
Water as a Hydride Source in Palladium‐Catalyzed Enantioselective Reductive Heck Reactions
inferredcites →https://doi.org/10.1002/ange.201706893openalex-snapshot
Allyl‐Palladium‐Catalyzed α,β‐Dehydrogenation of Carboxylic Acids via Enediolates
inferredcites →https://doi.org/10.1002/anie.201700195openalex-snapshot
Water as a Hydride Source in Palladium‐Catalyzed Enantioselective Reductive Heck Reactions
inferredcites →https://doi.org/10.1002/anie.201704146openalex-snapshot
Deuterium‐ and Tritium‐Labelled Compounds: Applications in the Life Sciences
inferredcites →https://doi.org/10.1002/anie.201706893openalex-snapshot
Allyl‐Palladium‐Catalyzed α,β‐Dehydrogenation of Carboxylic Acids via Enediolates
inferredcites →https://doi.org/10.1002/anie.201712775openalex-snapshot
Palladium‐Catalyzed Atom‐Transfer Radical Cyclization at Remote Unactivated C(sp3)−H Sites: Hydrogen‐Atom Transfer of Hybrid Vinyl Palladium Radical Intermediates
inferredcites →https://doi.org/10.1002/anie.201913825openalex-snapshot
Enantioselective Synthesis of 3‐Substituted Cyclobutenes by Catalytic Conjugate Addition/Trapping Strategies
inferredcites →https://doi.org/10.1002/asia.201800496openalex-snapshot
Non‐Bonding Interactions Enable the Selective Formation of Branched Products in Palladium‐Catalyzed Allylic Substitution Reactions
inferredcites →https://doi.org/10.1002/chem.201604585openalex-snapshot
Unsaturated Four‐Membered Rings: Efficient Strategies for the Construction of Cyclobutenes and Alkylidenecyclobutanes
inferredcites →https://doi.org/10.1002/chem.201803147openalex-snapshot
Stereodivergent Alkyne Reduction by using Water as the Hydrogen Source
inferredcites →https://doi.org/10.1002/chem.201903221openalex-snapshot
Ionic Pd/NHC Catalytic System Enables Recoverable Homogeneous Catalysis: Mechanistic Study and Application in the Mizoroki–Heck Reaction
inferredcites →https://doi.org/10.1002/chem.201903961openalex-snapshot
Annulative Allylic Alkylation Reactions between Dual Electrophiles and Dual Nucleophiles: Applications in Complex Molecule Synthesis
inferredcites →https://doi.org/10.1021/acs.jmedchem.8b01808openalex-snapshot
Applications of Deuterium in Medicinal Chemistry
inferredcites →https://doi.org/10.1021/acs.organomet.7b00657openalex-snapshot
Palladium-Catalyzed Reductive Cross-Coupling Reaction of Aryl Chromium(0) Fischer Carbene Complexes with Aryl Iodides
inferredcites →https://doi.org/10.1021/acs.orglett.6b01999openalex-snapshot
Diboron-Assisted Palladium-Catalyzed Transfer Hydrogenation of N-Heteroaromatics with Water as Hydrogen Donor and Solvent
inferredcites →https://doi.org/10.1021/acscatal.9b04871openalex-snapshot
Diastereo- and Enantioselective CuH-Catalyzed Hydroamination of Strained Trisubstituted Alkenes
inferredcites →https://doi.org/10.1021/cr020027wopenalex-snapshot
Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
inferredcites →https://doi.org/10.1021/ja0471424openalex-snapshot
Elucidating Reactivity Differences in Palladium-Catalyzed Coupling Processes: The Chemistry of Palladium Hydrides
inferredcites →https://doi.org/10.1021/jacs.6b02132openalex-snapshot
Tetrahydroxydiboron-Mediated Palladium-Catalyzed Transfer Hydrogenation and Deuteriation of Alkenes and Alkynes Using Water as the Stoichiometric H or D Atom Donor
inferredcites →https://doi.org/10.1021/ol070779iopenalex-snapshot
Unprecedented Hydrogen Transfer from Water to Alkenes and Alkynes Mediated by Ti III and Late Transition Metals
inferredcites →https://doi.org/10.1021/om060126qopenalex-snapshot
Theoretical Evidence for Low-Ligated Palladium(0): [Pd−L] as the Active Species in Oxidative Addition Reactions
inferredcites →https://doi.org/10.1039/c4cc10111aopenalex-snapshot
Unveiling the uncatalyzed reaction of alkynes with 1,2-dipoles for the room temperature synthesis of cyclobutenes
inferredcites →https://doi.org/10.1039/c8qo00358kopenalex-snapshot
Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes
inferredcites →https://doi.org/10.1039/c9cc00797kopenalex-snapshot
A palladium-catalyzed regiocontrollable hydroarylation reaction of allenamides with B 2 pin 2 /H 2 O
inferredcites →https://doi.org/10.1039/c9gc04184bopenalex-snapshot
Thermal [2 + 2]-cycloaddition between silylalkynes and allenylphenols followed by the nucleophilic addition of water: metal-free and economical synthesis of arylcyclobutenals
inferredcites →https://doi.org/10.1055/s-1996-4175openalex-snapshot
Palladium-Catalyzed Hydrogenolysis of Allylic and Propargylic Compounds with Various Hydrides
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ajoc.202400651openalex-snapshot
Solvent Effects in the Reactions of Alkenes with gem‐Bis(triflyl)ethylene
inferred← citeshttps://doi.org/10.1002/asia.70414openalex-snapshot
Synthetic Methods for Four‐Membered Carbocycles Bearing Emerging Fluorinated Motifs
inferred← citeshttps://doi.org/10.1002/chem.202200704openalex-snapshot
Synthesis of Spirocyclic Cyclobutenes through Desulfinative Spirocyclisation of gem‐Bis(triflyl)cyclobutenes
inferred← citeshttps://doi.org/10.1002/chem.202400843openalex-snapshot
HFIP‐Mediated Desulfinative Friedel–Crafts Cyclobutenylation Reaction
inferred← citeshttps://doi.org/10.1016/j.mcat.2023.113211openalex-snapshot
A theoretical study of the mechanisms, regio- and enantioselectivities associated with rhodium-catalyzed allylic alkylation reactions using hard benzylzinc nucleophiles
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.113905openalex-snapshot
Palladium-catalyzed remote allylation of styrene derivatives: DFT calculations unraveling regioselectivity controlled by non-covalent interactions
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02144openalex-snapshot
Asymmetric Synthesis of Bioactive Fluorinated Sulfonyl-Cyclobutene Derivatives via P(III)/P(V) Redox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01514openalex-snapshot
Unveiling the Use of 1,1-Bis(triflyl)ethylene as CF3SO2CH═CH2 Source with the Assistance of (n-Bu)4NF: Synthesis of 3-[(Trifluoromethyl)sulfonyl]cyclobut-1-enes
inferred← citeshttps://doi.org/10.1039/d1cc03087fopenalex-snapshot
Pd-catalyzed C(sp 3 )–C(sp) bond formation in iodocyclobutenes
inferred← citeshttps://doi.org/10.1039/d3qo00963gopenalex-snapshot
Transition-metal-free chemoselective reduction of α,β-unsaturated ketones using H 2 O as a hydrogen source
inferred← citeshttps://doi.org/10.1515/9783111739601-025openalex-snapshot
80924 Recent advances on transition metal-catalyzed Tsuji–Trost allylation
inferred← citeshttps://doi.org/10.3390/md22060253openalex-snapshot
Transition-Metal-Catalyzed Transformations for the Synthesis of Marine Drugs
inferred← citeshttps://doi.org/10.3390/molecules27217649openalex-snapshot
Efficient Synthesis of Fluorescent Coumarins and Phosphorous-Containing Coumarin-Type Heterocycles via Palladium Catalyzed Cross-Coupling Reactions
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