Tetraphosphine/palladium-catalyzed Suzuki-Miyaura coupling of heteroaryl halides with 3-pyridine- and 3-thiopheneboronic acid: an efficient catalyst for the formation of biheteroaryls-Reference-Cited by-同舟云学术

Tetraphosphine/palladium-catalyzed Suzuki-Miyaura coupling of heteroaryl halides with 3-pyridine- and 3-thiopheneboronic acid: an efficient catalyst for the formation of biheteroaryls

Published:2013-03-25 Issue:4 Volume:27 Page:232-238
ISSN:0268-2605
Container-title:Applied Organometallic Chemistry
language:en
Short-container-title:Appl. Organometal. Chem.

Author:

Wang Kun¹,Fu Qi¹,Zhou Rong¹,Zheng Xueli¹,Fu Haiyan¹,Chen Hua¹,Li Ruixiang¹

Affiliation:

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

Publisher

Wiley

Subject

Inorganic Chemistry,General Chemistry

Reference57 articles.

1. Chemical and Pharmacological Aspects of Heteroaryl-Nitrones

2. 2-Phenylimidazopyridines, a New Series of Golgi Compounds with Potent Antiviral Activity

3. Mass spectrometry as test bench for medicinal chemistry studies

4. Palladium-Catalyzed Cross-Coupling of Five-Membered Heterocyclic Silanolates

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