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Chiral N‐Heterocyclic Carbene Ligands Bearing a Pyridine Moiety for the Copper‐Catalyzed Alkylation of N‐Sulfonylimines with Dialkylzinc Reagents
Authors:Dr. Takahiro Soeta  Tomohiro Ishizaka  Yuta Tabatake  Prof. Dr. Yutaka Ukaji
Affiliation:Division of Material Chemistry, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa, 920‐1192 (Japan), Fax: (+81)?76‐264‐5742
Abstract:Amino acid‐derived chiral imidazolium salts, each bearing a pyridine ring, were developed as N‐heterocyclic carbene ligands. The copper‐catalyzed asymmetric alkylation of various N‐sulfonylimines with dialkylzinc reagents in the presence of these chiral imidazolium salts afforded the corresponding alkylated products with high enantioselectivity (up to 99 % ee). The addition of HMPA to the reaction mixture as a co‐solvent is critical in terms of chemical yield and enantioselectivity. A wide range of N‐sulfonylimines and dialkylzinc reagents were found to be applicable to this reaction.
Keywords:asymmetric alkylation  copper catalysis  enantioselectivity  N‐heterocyclic carbenes  N‐sulfonylimines
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