Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands.

scientific article published on 12 May 2017

Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1021/ACS.ORGLETT.7B01082
P932PMC publication ID5580394
P698PubMed publication ID28498667

P50authorStephen L. BuchwaldQ6134174
Bryan T IngogliaQ88049889
P2860cites workFormation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluoridesQ24626698
Negishi coupling of secondary alkylzinc halides with aryl bromides and chloridesQ24651734
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N-substituted 2-aminobiphenylpalladium methanesulfonate precatalysts and their use in C-C and C-N cross-couplingsQ33596995
Palladium-catalyzed hydroxylation of aryl and heteroaryl halides enabled by the use of a palladacycle precatalystQ33725567
Design and Preparation of New Palladium Precatalysts for C-C and C-N Cross-Coupling ReactionsQ34344343
Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalystQ34359682
Structure and Reactivity of [(L•Pd)n•(1,5-cyclooctadiene)] (n=1-2) Complexes Bearing Biaryl Phosphine LigandsQ34390681
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Design of New Ligands for the Palladium-Catalyzed Arylation of α-Branched Secondary AminesQ35812271
Dosage delivery of sensitive reagents enables glove-box-free synthesisQ35953656
A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcoholsQ36300984
A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and BromidesQ36486950
Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalystsQ36969049
A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chloridesQ36982977
Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligandsQ37030381
Addressing challenges in palladium-catalyzed cross-coupling reactions through ligand designQ38025590
C-N bond forming cross-coupling reactions: an overviewQ38146695
Applications of Palladium-Catalyzed C-N Cross-Coupling ReactionsQ38968855
Development of a Method for the N-Arylation of Amino Acid Esters with Aryl TriflatesQ41006996
The Evolution of Pd0/PdII-Catalyzed Aromatic FluorinationQ41517598
Generating Active "L-Pd(0)" via Neutral or Cationic π-Allylpalladium Complexes Featuring Biaryl/Bipyrazolylphosphines: Synthetic, Mechanistic, and Structure-Activity Studies in Challenging Cross-Coupling ReactionsQ46720578
Dual effect of halides in the Stille reaction: in situ halide metathesis and catalyst stabilizationQ85241497
P433issue11
P407language of work or nameEnglishQ1860
P304page(s)2853-2856
P577publication date2017-05-12
P1433published inOrganic LettersQ2396276
P1476titleOxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands
P478volume19

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cites work (P2860)
Q90363727An Improved PIII/PV═O-Catalyzed Reductive C-N Coupling of Nitroaromatics and Boronic Acids by Mechanistic Differentiation of Rate- and Product-Determining Steps
Q64938398Breaking the Base Barrier: An Electron-Deficient Palladium Catalyst Enables the Use of a Common Soluble Base in C-N Coupling.
Q91784350Mechanochemistry allows carrying out sensitive organometallic reactions in air: glove-box-and-Schlenk-line-free synthesis of oxidative addition complexes from aryl halides and palladium(0)
Q90073722Unexpected Formation of Hexasubstituted Arenes through a 2-fold Palladium-Mediated Ligand Arylation

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