| P50 | author | Fuk Yee Kwong | Q57015036 |
| P2093 | author name string | Albert S C Chan | |
| | Kin Shing Chan | |
| | Wai Har Lam | |
| | Chi Hung Yeung | |
| P2860 | cites work | A rationally designed universal catalyst for Suzuki-Miyaura coupling processes | Q44822908 |
| | Palladium/P,O-Ligand-Catalyzed Suzuki Cross-Coupling Reactions of Arylboronic Acids and Aryl Chlorides. Isolation and Structural Characterization of (P,O)-Pd(dba) Complex | Q44884387 |
| | Mild and efficient copper-catalyzed amination of aryl bromides with primary alkylamines. | Q50325229 |
| | Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998 | Q56482589 |
| | Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions | Q56482608 |
| | Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis | Q56587424 |
| | A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides | Q56688213 |
| | Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature | Q56688216 |
| | A novel class of amide-derived air-stable P,O-ligands for Suzuki cross-coupling at low catalyst loading | Q58479764 |
| | A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides | Q29395714 |
| | Solution-Phase Synthesis of a Thiazoyl-Substituted Indolyl Library via Suzuki Cross-Coupling | Q33194784 |
| | A New Highly Efficient Catalyst System for the Coupling of Nonactivated and Deactivated Aryl Chlorides with Arylboronic Acids Palladium-Catalyzed Reactions for Fine Chemical Synthesis, Part 17. The authors thank C. Fuhrmann for the excellent support | Q34512033 |
| | Palladium-catalyzed coupling reactions of aryl chlorides | Q34998714 |
| | Beyond thermodynamic acidity: a perspective on the complex-induced proximity effect (CIPE) in deprotonation reactions | Q35755716 |
| | A highly active Suzuki catalyst for the synthesis of sterically hindered biaryls: novel ligand coordination | Q43883566 |
| | Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C[bond]C, C[bond]N, and C[bond]O bond-forming cross-couplings | Q44086210 |
| | Synthesis and application of arylmonophosphinoferrocene ligands: ultrafast asymmetric hydrosilylation of styrene | Q44210088 |
| | A dicoordinate palladium(0) complex with an unusual intramolecular eta(1)-arene coordination | Q44488761 |
| | The First General Palladium Catalyst for the Suzuki−Miyaura and Carbonyl Enolate Coupling of Aryl Arenesulfonates | Q44593516 |
| | Insights into the Origin of High Activity and Stability of Catalysts Derived from Bulky, Electron-Rich Monophosphinobiaryl Ligands in the Pd-Catalyzed C−N Bond Formation | Q44651302 |
| | A ferrocene based palladacyclic precatalyst for the Suzuki cross-coupling of aryl chlorides | Q44712097 |
| | Practical synthesis of new and highly efficient ligands for the Suzuki reaction of aryl chlorides | Q44737616 |
| | Synthesis of aryl- and heteroaryl-substituted 3-benzyloxyisothiazoles via Suzuki and Negishi cross-coupling reactions | Q44763308 |
| P433 | issue | 17 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 2 | |
| P304 | page(s) | 1922-1923 | |
| P577 | publication date | 2004-07-28 | |
| P1433 | published in | Chemical Communications | Q426303 |
| P1476 | title | A simple and highly efficient P,O-type ligand for Suzuki-Miyaura cross-coupling of aryl halides | |