Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 69, Issue 22, Pages 7779-7782Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo048963u
Keywords
-
Categories
Ask authors/readers for more resources
Ferrocenyl monophosphine ligands have been developed by a method based on palladium-catalyzed Suzuki-Miyaura coupling. The modular procedure creates a rapid synthesis of phosphines with diverse properties. The electron-rich phosphines have been successfully applied to the Suzuki-Miyaura coupling of activated and deactivated aryl chlorides, with low catalyst loading being feasible in the synthesis of tris-ortho-substituted biaryls.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available