23754-24-7Relevant academic research and scientific papers
Palladium-Catalyzed Direct Cross-Coupling of Carboranyllithium with (Hetero)Aryl Halides
Lu, Ju-You,Wan, Hong,Zhang, Jianwei,Wang, Zhixuan,Li, Yang,Du, Yongmei,Li, Chunying,Liu, Zhao-Tie,Liu, Zhong-Wen,Lu, Jian
, p. 17542 - 17546 (2016)
A palladium-catalyzed direct C-arylation reaction of readily available cage carboranyllithium reagents with aryl halides has been developed for the first time. This method is applicable to a wide range of aryl halide substrates including aryl iodides, aryl bromides, and heteroaromatic halides.
Light-promoted copper-catalyzed cage C-Arylation of: O-carboranes: facile synthesis of 1-Aryl-o-carboranes and o-carborane-fused cyclics
Lu, Zhenpin,Ni, Hangcheng,Xie, Zuowei
supporting information, p. 14944 - 14948 (2021/09/04)
Light-promoted, copper catalyzed cage C-H arylation of o-carboranes with aryl halides has been achieved, leading to the facile synthesis of a variety of 1-Aryl-o-carboranes and o-carborane-fused cyclics. This method has the following features: (1) using o
Nickel-catalyzed cross-coupling reactions of o-carboranyl with aryl iodides: Facile synthesis of 1-aryl-o-carboranes and 1,2-diaryl-o-carboranes
Tang, Cen,Xie, Zuowei
supporting information, p. 7662 - 7665 (2015/06/25)
A nickel-catalyzed arylation at the carbon center of o-carborane cages has been developed, thus leading to the preparation of a series of 1-aryl-o-carboranes and 1,2-diaryl-o-carboranes in high yields upon isolation. This method represents the first examp
