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Abstract Chiral cyclopentadienyl (Cp x ) ligands have a large application potential in enantioselective transition‐metal catalysis. However, the development of concise and practical routes to such ligands remains in its infancy. We present a convenient and efficient two‐step synthesis of a novel class of chiral Cp x ligands with tunable steric properties that can be readily used for complexation, giving Cp x Rh I , Cp x Ir I , and Cp x Ru II complexes. The potential of this ligand class is demonstrated with the latter in the enantioselective cyclization of azabenzonorbornadienes with alkynes, affording dihydrobenzoindoles in up to 98:2 e.r., significantly outperforming existing binaphthyl‐derived Cp x ligands.
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Shouguo Wang
Anhui University
Sung Hwan Park
Chemical Synthesis Lab
Nicolai Cramer
Chemical Synthesis Lab
Angewandte Chemie International Edition
École Polytechnique Fédérale de Lausanne
Chemical Synthesis Lab
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Wang et al. (Mon,) studied this question.
synapsesocial.com/papers/6a078530f8ea14d3ccc64010 — DOI: https://doi.org/10.1002/anie.201802244