The palladium-catalyzed cross-coupling reaction between organoboron compounds and
organic halides or triflates provides a powerful and general methodology for the formation of …

This review with 206 references covers the literature published until March 2004 on the
development and applications of new efficient catalyst systems for the Suzuki palladium …

Nanosized palladium colloids, generated in situ by reduction of PdII to Pd0 [Eq.(a)], are
involved in the catalysis of phosphane‐free Heck and Suzuki reactions with simple …

Transition Metal Reagents and Catalysts Innovations in Organic Synthesis Jiro Tsuji
Emeritus Professor, Tokyo Institute of Technology, Japan Numerous innovative and practical …

Palladium-Catalyzed Suzuki-Type Self-Coupling of Arylboronic Acids. A Mechanistic Study |
The Journal of Organic Chemistry ACS ACS Publications C&EN CAS Find my institution Log In …

Polyfunctional biaryls are prepared by a modified Suzuki cross-coupling reaction between
arylboronic acids or sodium tetraphenylborate and aryl halides ArX, X I, Br, Cl in aqueous …

The cross-coupling of allylic electrophiles with boronic acids and boronates is extremely
useful for the formation of CÀC bonds and for the introduction of the allyl moieties to target …

Palladacycles derived from phenone-oximes 1 are efficient precatalysts for the Suzuki–
Miyaura coupling of arylboronic acids with aromatic and heteroaromatic bromides and …

A simplified synthesis of N-heterocyclic carbene (NHC) Pd-carboxylate complexes and their
activity in Suzuki− Miyaura cross-coupling reactions are described. Coupling of sterically …

The cyclisation-anion capture protocol has been applied to a wide range of starter and
terminating species to effect regio-and stereo-specific mono-and bis-cyclisation processes in …