A General, Efficient, and Functional-Group-Tolerant Catalyst System for the Palladium-Catalyzed Thioetherification of Aryl Bromides and Iodides
- 20 January 2009
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 74 (4) , 1663-1672
- https://doi.org/10.1021/jo802594d
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Discovery and Understanding of Transition-Metal-Catalyzed Aromatic Substitution ReactionsSynlett, 2006
- New Arylthioindoles: Potent Inhibitors of Tubulin Polymerization. 2. Structure−Activity Relationships and Molecular Modeling StudiesJournal of Medicinal Chemistry, 2006
- Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann ReactionChemical Reviews, 2002
- Palladium-catalysed reactions of aryl halides with soft, non-organometallic nucleophilesTetrahedron, 2002
- Practical Palladium Catalysts for C-N and C-O Bond FormationPublished by Springer Nature ,2002
- Metal-Catalyzed Carbon−Sulfur Bond FormationChemical Reviews, 2000
- Palladium-catalyzed amination of aryl halides and sulfonatesJournal of Organometallic Chemistry, 1999
- Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond FormationAccounts of Chemical Research, 1998
- Carbon−Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and SulfidesAccounts of Chemical Research, 1998
- Transition Metal Catalyzed Synthesis of Arylamines and Aryl Ethers from Aryl Halides and Triflates: Scope and MechanismAngewandte Chemie International Edition in English, 1998