The Triple Role of Fluoride Ions in Palladium-Catalyzed Suzuki-Miyaura Reactions: Unprecedented Transmetalation from [ArPdFL2] Complexes

Kinetic Data for the Transmetalation/Reductive Elimination in Palladium-Catalyzed Suzuki-Miyaura Reactions: Unexpected Triple Role of Hydroxide Ions Used as Base

(2011) Christian Amatore et al.   CHEMISTRY-A EUROPEAN JOURNAL

The Influence of Alkenes as π -Acidic Ligands in Pd-Catalysed Cross-Couplings

(2011) Amanda G. Jarvis et al.   CURRENT ORGANIC CHEMISTRY

Distinguishing Between Pathways for Transmetalation in Suzuki−Miyaura Reactions

(2011) Brad P. Carrow et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Role of a base in Suzuki-Miyaura reaction

(2011) A. F. Schmidt et al.   RUSSIAN JOURNAL OF GENERAL CHEMISTRY

Aryl Trifluoroborates in Suzuki-Miyaura Coupling: The Roles of Endogenous Aryl Boronic Acid and Fluoride

(2010) Mike Butters et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

The Slow-Release Strategy in Suzuki-Miyaura Coupling

(2010) Alastair J. J. Lennox et al.   ISRAEL JOURNAL OF CHEMISTRY

Organotrifluoroborates and Monocoordinated Palladium Complexes as Catalysts—A Perfect Combination for Suzuki–Miyaura Coupling

(2009) Gary A. Molander et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Non-conventional methodologies for transition-metal catalysed carbon–carbon coupling: a critical overview. Part 2: The Suzuki reaction

(2007) Francisco Alonso et al.   TETRAHEDRON