NC-palladacycles as highly effective cheap precursors for the phosphine-free Heck reactions
- 1 March 2001
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 622 (1-2), 89-96
- https://doi.org/10.1016/s0022-328x(00)00876-7
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Sulfur-Containing Palladacycles as Catalyst Precursors for the Heck ReactionOrganic Letters, 2000
- Heck reactions: a caveat on the use of palladium(II) PCP-type catalystsTetrahedron Letters, 1999
- The synthesis of a new palladacycle catalyst. Development of a high performance catalyst for Heck reactionsTetrahedron Letters, 1999
- Tridentate SCS Palladium(II) Complexes: New, Highly Stable, Recyclable Catalysts for the Heck ReactionJournal of the American Chemical Society, 1999
- Application of palladacycles in Heck type reactionsJournal of Organometallic Chemistry, 1999
- Orthopalladated triarylphosphite complexes as highly efficient catalysts in the Heck reactionTetrahedron Letters, 1998
- Highly active, stable, catalysts for the Heck reaction; further suggestions on the mechanismChemical Communications, 1998
- Highly Active Pd(II) PCP-Type Catalysts for the Heck ReactionJournal of the American Chemical Society, 1997
- Bidentate Nitrogen Ligands in Heck Type ReactionsSynlett, 1992
- Arylation of Olefin with Aryl Iodide Catalyzed by PalladiumBulletin of the Chemical Society of Japan, 1971