Iron-Catalyzed Direct Suzuki–Miyaura Reaction: Theoretical and Experimental Studies on the Mechanism and the Regioselectivity-Reference-Cited by-同舟云学术

Iron-Catalyzed Direct Suzuki–Miyaura Reaction: Theoretical and Experimental Studies on the Mechanism and the Regioselectivity

Published:2012-07-26 Issue:8 Volume:2 Page:1829-1837
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Dong Liang¹,Wen Jun¹,Qin Song¹,Yang Na¹,Yang Huaqing¹,Su Zhishan¹,Yu Xiaoqi¹,Hu Changwei¹

Affiliation:

1. Key Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, People's Republic of China

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cs300028y

Reference80 articles.

1. The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases

2. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

3. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

4. Mutual Activation: Suzuki-Miyaura Coupling through Direct Cleavage of the sp2 CO Bond of Naphtholate

5. Suzuki–Miyaura Coupling Reaction by PdII-Catalyzed Aromatic CH Bond Activation Directed by anN-Alkyl Acetamino Group

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