Sterically Hindered Chelating Alkyl Phosphines Provide Large Rate Accelerations in Palladium-Catalyzed Amination of Aryl Iodides, Bromides, and Chlorides, and the First Amination of Aryl Tosylates
Author:
Affiliation:
1. Department of Chemistry, Yale University P.O. Box 208107, New Haven, Connecticut 06520-8107
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja981318i
Reference25 articles.
1. Palladium Alkoxides: Potential Intermediacy in Catalytic Amination, Reductive Elimination of Ethers, and Catalytic Etheration. Comments on Alcohol Elimination from Ir(III)
2. Synthesis of Oxygen Heterocycles via a Palladium-Catalyzed C−O Bond-Forming Reaction
3. Palladium-Catalyzed Intermolecular Carbon−Oxygen Bond Formation: A New Synthesis of Aryl Ethers
4. Transformations of Chloroarenes, Catalyzed by Transition-Metal Complexes
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