Article ID Journal Published Year Pages File Type
1325903 Journal of Organometallic Chemistry 2008 9 Pages PDF
Abstract

A series of N-alkyl-substituted cyclopalladated ferrocenylimines were used in palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl halides in room temperature and CH3OH/H2O media under aerobic conditions. As for the catalysts, the length of N-alkyl chains has no significant effect on the catalytic activity. Using 0.01 mol% of dimer 3a in the presence of K2CO3 as base offered excellent yields in the reaction of activated and non-activated aryl bromides with phenylboronic acid.

Graphical abstractA series of N-alkyl-substituted cyclopalladated ferrocenylimines were used in palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl halides in room temperature and CH3OH/H2O media under aerobic conditions. Good to excellent yields were obtained with lower catalyst loading and short reaction time.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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