Electrochemically Driven, Ni-Catalyzed Aryl Amination: Scope, Mechanism, and Applications-Reference-Cited by-同舟云学术

Electrochemically Driven, Ni-Catalyzed Aryl Amination: Scope, Mechanism, and Applications

Published:2019-03-24 Issue:15 Volume:141 Page:6392-6402
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kawamata Yu¹²,Vantourout Julien C.¹^ORCID,Hickey David P.³²^ORCID,Bai Peng⁴²^ORCID,Chen Longrui⁵,Hou Qinglong⁵,Qiao Wenhua⁵,Barman Koushik³²,Edwards Martin A.³²^ORCID,Garrido-Castro Alberto F.¹^ORCID,deGruyter Justine N.¹^ORCID,Nakamura Hugh¹,Knouse Kyle¹^ORCID,Qin Chuanguang¹,Clay Khalyd J.¹,Bao Denghui⁵,Li Chao¹^ORCID,Starr Jeremy T.⁶^ORCID,Garcia-Irizarry Carmen⁶,Sach Neal⁷,White Henry S.³²^ORCID,Neurock Matthew⁴²,Minteer Shelley D.³²^ORCID,Baran Phil S.¹²^ORCID

Affiliation:

1. Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States

2. Center for Synthetic Organic Electrochemistry, 315 South 1400 East, Salt Lake City, Utah 84112, United States

3. Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112, United States

4. Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States

5. Asymchem Life Science (Tianjin), Tianjin Economic-Technological Development Zone, Tianjin 300457, China

6. Discovery Sciences, Medicine Design, Pfizer Global Research and Development, 445 Eastern Point Road, Groton, Connecticut 06340, United States

7. Department of Chemistry, La Jolla Laboratories, Pfizer, 10770 Science Center Drive, San Diego, California 92121, United States

Funder

Foundation for the National Institutes of Health

Division of Chemistry

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

http://pubs.acs.org/doi/pdf/10.1021/jacs.9b01886

Reference66 articles.

1. Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions

2. The Complementary Competitors: Palladium and Copper in C–N Cross-Coupling Reactions

3. Palladium- and copper-mediated N-aryl bond formation reactions for the synthesis of biological active compounds

4. Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

5. Breaking the Base Barrier: An Electron-Deficient Palladium Catalyst Enables the Use of a Common Soluble Base in C–N Coupling

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