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Research Highlights

A novel "Kabuto-like" nickel catalyst forms bioactive frameworks from low-cost phenol derivatives

Abstract:

Researchers at ITbM, Nagoya University developed a new nickel catalyst with a "Kabuto-like" structure that was found to catalyze the cross-coupling reaction between carbonyl compounds and readily available phenol derivatives, to form α-arylketones, which are found in many biologically active compounds (Kabuto = a helmet worn by Japanese samurai).

Fig1_Frameworks.jpg Fig2_Ligands.jpg

Journal Information:

"Nickel-Catalyzed α-Arylation of Ketones with Phenol Derivatives" Ryosuke Takise, Kei Muto, Junichiro Yamaguchi and Kenichiro Itami, Angewandte Chemie International Edition (2014)

DOI:10.1002/anie.201403823

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