Sulfur-Containing Palladacycles: Efficient Phosphine-Free Catalyst Precursors for the Suzuki Cross-Coupling Reaction at Room Temperature
- 4 August 2000
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 2 (18) , 2881-2884
- https://doi.org/10.1021/ol0063048
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild ConditionsJournal of the American Chemical Society, 2000
- Tridentate SCS Palladium(II) Complexes: New, Highly Stable, Recyclable Catalysts for the Heck ReactionJournal of the American Chemical Society, 1999
- Microwave-Assisted Aqueous Suzuki Cross-Coupling ReactionsThe Journal of Organic Chemistry, 1999
- Cationic cyclopalladated complexes: new catalyst precursors for the telomerization of butadiene with alcoholsJournal of Molecular Catalysis A: Chemical, 1996
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995
- Regioselectivity of the Insertion of 4,4-Dimethyl-2-Pentyne into the Pd-C Bond of Cyclopalladated ComplexesOrganometallics, 1995
- Synthetic studies via the cross-coupling reaction of organoboron derivatives with organic halidesPure and Applied Chemistry, 1991
- Reactions of cyclopalladated compounds. Part 21. Various examples of sulphur-assisted intramolecular palladation of aryl and alkyl groupsJ. Chem. Soc., Dalton Trans., 1989
- Cyclopalladated CompoundsPublished by Wiley ,1989
- Direct synthesis of thio ethers from thiols and alcoholsThe Journal of Organic Chemistry, 1983