A Ligand Exchange Process for the Diversification of Palladium Oxidative Addition Complexes
“A Ligand Exchange Process for the Diversification of Palladium Oxidative Addition Complexes”, Org. Lett., 2021, 23, 6030-6034.
C—C (Suzuki–Miyaura)
Catalytic Asymmetric Synthesis of α-Arylpyrrolidines and Benzo-fused Nitrogen Heterocycles
“Catalytic Asymmetric Synthesis of α-Arylpyrrolidines and Benzo-fused Nitrogen Heterocycles”, Angew. Chem. Int. Ed., 2019, 58(11), 3407-3411.
Suzuki-Miyaura cross-coupling optimization enabled by automated feedback
“Suzuki-Miyaura cross-coupling optimization enabled by automated feedback”, Reaction Chemistry & Engineering, 2016, 1, 658-666 .
A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides
“A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides”, J. Am. Chem. Soc., 1998, 120(37), 9722-9723.
Continuous-flow synthesis of biaryls enabled by multistep solid-handling in a lithiation/borylation/Suzuki-Miyaura cross-coupling sequence
“Continuous-flow synthesis of biaryls enabled by multistep solid-handling in a lithiation/borylation/Suzuki-Miyaura cross-coupling sequence”, Angew. Chem. Int. Ed., 2011, 50(45), 10665-10669.
A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides
“A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides”, Angew. Chem. Int. Ed., 1999, 38(16), 2413-2416.
A General and Efficient Method for the Suzuki–Miyaura Coupling of 2-Pyridyl Nucleophiles
“A General and Efficient Method for the Suzuki–Miyaura Coupling of 2-Pyridyl Nucleophiles”, Angew. Chem. Int. Ed., 2008, 47(25), 4695-4698.
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