Highly Active Palladium Catalysts for Suzuki Coupling Reactions
- 1 October 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (41) , 9550-9561
- https://doi.org/10.1021/ja992130h
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Highly Active Ruthenium Catalysts for Olefin Metathesis: The Synergy of N‐Heterocyclic Carbenes and Coordinatively Labile LigandsAngewandte Chemie International Edition in English, 1999
- Novel Electron-Rich Bulky Phosphine Ligands Facilitate the Palladium-Catalyzed Preparation of Diaryl EthersJournal of the American Chemical Society, 1999
- Synthesis of 4-substituted phenylalanines by cross-coupling reactions: Extension of the methodology to aryl chloridesTetrahedron Letters, 1998
- Industrial Aqueous Biphasic Catalysis: Status and DirectionsOrganic Process Research & Development, 1998
- Investigations into ambient temperature biaryl coupling reactionsTetrahedron, 1997
- Suzuki-type coupling of chloroarenes with arylboronic acids catalysed by nickel complexesTetrahedron Letters, 1997
- Carbenoid or Lithium Complex of a Carbanion? Synthesis and Structure of (Me3Si)2CP(aryl)C(Cl)Li(thf)3 and LiCl Elimination To Give the PhosphireneAngewandte Chemie International Edition in English, 1995
- Transformations of Chloroarenes, Catalyzed by Transition-Metal ComplexesChemical Reviews, 1994
- High yields of unsymmetrical biaryls via cross coupling of arylboronic acids with haloarenes using a modified Suzuki-Beletskaya procedureJournal of the Chemical Society, Chemical Communications, 1994
- Dramatic rate enhancement of Suzuki diene synthesis. Its application to palytoxin synthesisJournal of the American Chemical Society, 1987