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-Reference-Cited by-同舟云学术

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

Published:1998-07-01 Issue:29 Volume:120 Page:7369-7370
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hamann Blake C.¹,Hartwig John F.¹

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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