scholarly article | Q13442814 |
P50 | author | Stephen L. Buchwald | Q6134174 |
Bryan T Ingoglia | Q88049889 | ||
P2860 | cites work | Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluorides | Q24626698 |
Negishi coupling of secondary alkylzinc halides with aryl bromides and chlorides | Q24651734 | ||
Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. | Q31162349 | ||
N-substituted 2-aminobiphenylpalladium methanesulfonate precatalysts and their use in C-C and C-N cross-couplings | Q33596995 | ||
Palladium-catalyzed hydroxylation of aryl and heteroaryl halides enabled by the use of a palladacycle precatalyst | Q33725567 | ||
Design and Preparation of New Palladium Precatalysts for C-C and C-N Cross-Coupling Reactions | Q34344343 | ||
Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalyst | Q34359682 | ||
Structure and Reactivity of [(L•Pd)n•(1,5-cyclooctadiene)] (n=1-2) Complexes Bearing Biaryl Phosphine Ligands | Q34390681 | ||
Studying regioisomer formation in the Pd-catalyzed fluorination of aryl triflates by deuterium labeling | Q34489910 | ||
Design of New Ligands for the Palladium-Catalyzed Arylation of α-Branched Secondary Amines | Q35812271 | ||
Dosage delivery of sensitive reagents enables glove-box-free synthesis | Q35953656 | ||
A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols | Q36300984 | ||
A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides | Q36486950 | ||
Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts | Q36969049 | ||
A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides | Q36982977 | ||
Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands | Q37030381 | ||
Addressing challenges in palladium-catalyzed cross-coupling reactions through ligand design | Q38025590 | ||
C-N bond forming cross-coupling reactions: an overview | Q38146695 | ||
Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions | Q38968855 | ||
Development of a Method for the N-Arylation of Amino Acid Esters with Aryl Triflates | Q41006996 | ||
The Evolution of Pd0/PdII-Catalyzed Aromatic Fluorination | Q41517598 | ||
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 Reactions | Q46720578 | ||
Dual effect of halides in the Stille reaction: in situ halide metathesis and catalyst stabilization | Q85241497 | ||
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2853-2856 | |
P577 | publication date | 2017-05-12 | |
P1433 | published in | Organic Letters | Q2396276 |
P1476 | title | Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands | |
P478 | volume | 19 |
Q90363727 | An Improved PIII/PV═O-Catalyzed Reductive C-N Coupling of Nitroaromatics and Boronic Acids by Mechanistic Differentiation of Rate- and Product-Determining Steps |
Q64938398 | Breaking the Base Barrier: An Electron-Deficient Palladium Catalyst Enables the Use of a Common Soluble Base in C-N Coupling. |
Q91784350 | Mechanochemistry 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) |
Q90073722 | Unexpected Formation of Hexasubstituted Arenes through a 2-fold Palladium-Mediated Ligand Arylation |
Search more.