Sonogashira Cross-Coupling of Aryl Ammonium Salts by Selective C–N Activation Catalyzed by Air- and Moisture-Stable, Highly Active [Pd(NHC)(3-CF<sub>3</sub>-An)Cl<sub>2</sub>] (An = Aniline) Precatalysts-Reference-Cited by-同舟云学术

Sonogashira Cross-Coupling of Aryl Ammonium Salts by Selective C–N Activation Catalyzed by Air- and Moisture-Stable, Highly Active [Pd(NHC)(3-CF₃-An)Cl₂] (An = Aniline) Precatalysts

Published:2022-08-24 Issue:34 Volume:24 Page:6310-6315
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lei Peng¹²³^ORCID,Wang Yibo¹,Zhang Caixia¹,Hu Yuge¹,Feng Juntao¹²^ORCID,Ma Zhiqing¹²,Liu Xili¹³,Szostak Roman⁴,Szostak Michal⁵^ORCID

Affiliation:

1. College of Plant Protection, Northwest A&F University, Yangling, Shaanxi 712100, China

2. Shaanxi Research Center of Biopesticide Engineering & Technology, Northwest A&F University, Yangling, Shaanxi 712100, China

3. State Key Laboratory of Crop Stress Biology for Arid Areas, Northwest A&F University, Yangling, Shaanxi 712100, China

4. Department of Chemistry, Wroclaw University, F. Joliot-Curie 14, Wroclaw 50-383, Poland

5. Department of Chemistry, Rutgers University, 73 Warren Street, Newark, New Jersey 07102, United States

Funder

Rutgers, The State University of New Jersey

National Natural Science Foundation of China

National Science Foundation

Technology Innovation Guidance Special Fund of Shaanxi Province

Wroclaw Center for Networking and Supercomputing

Innovation Capability Support Plan of Shaanxi Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c02534

Reference45 articles.

1. Recent Methodologies That Exploit Oxidative Addition of C–N Bonds to Transition Metals

2. Transition-Metal-Catalyzed Cleavage of C–N Single Bonds

3. Transition-metal catalysed C–N bond activation

4. Transition Metal-Catalyzed Activation of Aliphatic C−X Bonds in Carbon−Carbon Bond Formation

5. Accessing Medicinally Relevant O ‐Benzofused Heterocycles through C−X Activation: Recent Trends

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