Iridium-Catalyzed Enantioselective CH Alkylation of Ferrocenes with Alkenes Using Chiral Diene Ligands

The first catalytic and enantioselective CH alkylation of ferrocene derivatives with various alkenes was achieved. A cationic iridium complex, having a chiral diene ligand, and an isoquinolyl moiety as a directing group are essential for regioselective and enantioselective CH bond activation. Dire...

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Veröffentlicht in:Angewandte Chemie International Edition 2014-05, Vol.53 (21), p.5410-5413
Hauptverfasser: Shibata, Takanori, Shizuno, Tsubasa
Format: Artikel
Sprache:eng
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Zusammenfassung:The first catalytic and enantioselective CH alkylation of ferrocene derivatives with various alkenes was achieved. A cationic iridium complex, having a chiral diene ligand, and an isoquinolyl moiety as a directing group are essential for regioselective and enantioselective CH bond activation. Director's cut: The first catalytic and enantioselective CH alkylation of ferrocene derivatives with various alkenes was achieved. A cationic iridium complex, having a chiral diene ligand, and an isoquinolyl moiety as a directing group are essential for regioselective and enantioselective CH bond activation. coe=cyclooctene, NaBARF=sodium tetrakis[3,5‐bis(trifluoromethyl)phenyl]borate.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201402518