Nickel-catalyzed C-O activation of phenol derivatives with potassium heteroaryltrifluoroborates

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Nickel-catalyzed C-O activation of phenol derivatives with potassium heteroaryltrifluoroborates is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1021/OL101592R
P932PMC publication ID2937100
P698PubMed publication ID20715841
P5875ResearchGate publication ID45693877

P50authorGary A. MolanderQ74963225
P2093author name stringFloriane Beaumard
P2860cites workPalladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.Q31162349
Organotrifluoroborates and monocoordinated palladium complexes as catalysts--a perfect combination for Suzuki-Miyaura couplingQ34051116
Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structureQ34407125
Scope of the Suzuki-Miyaura cross-coupling reactions of potassium heteroaryltrifluoroboratesQ37146977
A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylatesQ37381970
Suzuki-Miyaura coupling of aryl carbamates, carbonates, and sulfamatesQ42944115
N,N-diethyl O-carbamate: directed metalation group and orthogonal Suzuki-Miyaura cross-coupling partnerQ43238008
Cross-coupling reactions of aryl pivalates with boronic acidsQ44567560
The First General Palladium Catalyst for the Suzuki−Miyaura and Carbonyl Enolate Coupling of Aryl ArenesulfonatesQ44593516
NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acidsQ44887549
A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.Q46030717
Biaryl construction via Ni-catalyzed C-O activation of phenolic carboxylatesQ46321669
Suzuki-Miyaura coupling of aryl tosylates catalyzed by an array of indolyl phosphine-palladium catalysts.Q46376635
Palladium-catalyzed Suzuki-Miyaura cross-couplings of aryl tosylates with potassium aryltrifluoroboratesQ46920091
Nickel-catalyzed cross-coupling of aryl methyl ethers with aryl boronic esters.Q47690708
Nickel-catalyzed efficient and practical Suzuki-Miyaura coupling of alkenyl and aryl carbamates with aryl boroxines.Q50568427
A general palladium-catalyzed Suzuki-Miyaura coupling of aryl mesylates.Q52693544
Mechanism of Ni-catalyzed selective C-O bond activation in cross-coupling of aryl esters.Q52697737
NiCl(2)(PCy(3))(2): a simple and efficient catalyst precursor for the Suzuki cross-coupling of aryl tosylates and arylboronic acidsQ74507235
Room-temperature Ni0-catalyzed cross-coupling reactions of aryl arenesulfonates with arylboronic acidsQ79759781
Synthesis, inhibition and binding of simple non-nitrogen inhibitors of monoamine transportersQ80186175
C-C bond formation catalyzed heterogeneously by nickel-on-graphite (Ni/Cg)Q80685316
A general palladium catalyst system for Suzuki-Miyaura coupling of potassium aryltrifluoroborates and aryl mesylatesQ84506208
P433issue18
P407language of work or nameEnglishQ1860
P921main subjectnickelQ744
P304page(s)4022-4025
P577publication date2010-09-01
P1433published inOrganic LettersQ2396276
P1476titleNickel-catalyzed C-O activation of phenol derivatives with potassium heteroaryltrifluoroborates
P478volume12

Reverse relations

cites work (P2860)
Q382631584-(Naphthalen-1-yl)pyridine
Q56482600A Highly Practical and Reliable Nickel Catalyst for Suzuki-Miyaura Coupling of Aryl Halides
Q37833010Activation of "inert" alkenyl/aryl C-O bond and its application in cross-coupling reactions.
Q58344475Aryl Ether as a Negishi Coupling Partner: An Approach for Constructing CC Bonds under Mild Conditions
Q35147938Cross-coupling of mesylated phenol derivatives with potassium alkoxymethyltrifluoroborates
Q34609427Cross-coupling of mesylated phenol derivatives with potassium ammonio- and amidomethyltrifluoroborates
Q35250631Cross-coupling of mesylated phenol derivatives with potassium cyclopropyltrifluoroborate
Q34388356Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates
Q49979276Efficient Ni-catalyzed conversion of phenols protected with 2,4,6-trichloro-1,3,5-triazine (TCT) to olefins
Q45713343Iron-catalyzed N-alkylation using π-activated ethers as electrophiles
Q92145404Ligation state of nickel during C-O bond activation with monodentate phosphines
Q46820136Mechanism of Ni N-heterocyclic carbene catalyst for C-O bond hydrogenolysis of diphenyl ether: a density functional study
Q50517812Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp2 C-O bond of naphtholate.
Q48253862Ni-Catalyzed Stannylation of Aryl Esters via C-O Bond Cleavage
Q38940338Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C-O Bond Activation
Q91778493Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles
Q34663409Nickel-catalyzed cross-couplings involving carbon-oxygen bonds
Q53545462Palladium dichloride adduct of N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine: synthesis, structure and catalytic performance in the decarboxylative cross-coupling of 4-picolinic acid with aryl bromide.
Q92930482Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Tosylates
Q41587578Palladium-catalysed cross-coupling reaction of ultra-stabilised 2-aryl-1,3-dihydro-1H-benzo[d]1,3,2-diazaborole compounds with aryl bromides: A direct protocol for the preparation of unsymmetrical biaryls.
Q43428282Palladium-catalyzed Suzuki-Miyaura coupling of aryl sulfamates with arylboronic acids
Q50508476Palladium-catalyzed desulfitative C-H arylation of heteroarenes with sodium sulfinates.
Q42671822Pd-catalyzed Suzuki-Miyaura cross-coupling reactions between sulfamates and potassium Boc-protected aminomethyltrifluoroborates
Q46446831Sustainable Fe-ppm Pd nanoparticle catalysis of Suzuki-Miyaura cross-couplings in water
Q34962552Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies
Q36186011Suzuki-Miyaura cross-coupling reactions of potassium Boc-protected aminomethyltrifluoroborate with aryl and hetaryl mesylates
Q37400739The Pyridyldiisopropylsilyl Group: A Masked Functionality and Directing Group for Monoselective ortho-Acyloxylation and ortho-Halogenation Reactions of Arenes.

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