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We report herein the first examples of catalytic enantioselective synthesis of axially chiral 3-arylpyrroles. Reaction of α-isocyanoacetates with β-aryl-α,β-alkynic ketones in the presence of silver oxide and a phosphine ligand derived from Cinchona alkaloid occurred chemoselectively to afford enantioenriched 3-arylpyrroles in high yields with excellent enantiomeric excesses. The pyrrole ring was constructed de novo in this process.
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Zheng et al. (Tue,) studied this question.
synapsesocial.com/papers/6a0867d4113ba5b476de23f5 — DOI: https://doi.org/10.1002/anie.201812654
Sheng‐Cai Zheng
Qian Wang
Jieping Zhu
Angewandte Chemie International Edition
École Polytechnique Fédérale de Lausanne
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