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Enantioselective synthesis of N-N biaryl atropisomers is an emerging area but remains underexplored. The development of efficient synthesis of N-N biaryl atropisomers is in great demand. Herein, the construction of N-N biaryl atropisomers through iridium-catalyzed asymmetric C-H alkylation is reported for the first time. In the presence of readily available Ir precursor and Xyl-BINAP, a variety of axially chiral molecules based on indole-pyrrole skeleton were obtained in good yields (up to 98 %) with excellent enantioselectivity (up to 99 % ee). In addition, N-N bispyrrole atropisomers could also be synthesized in excellent yields and enantioselectivity. This method features perfect atom economy, wide substrate scope, and multifunctionalized products allowing diverse transformations.
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Si‐Yong Yin
Shanghai Institute of Organic Chemistry
Qiansujia Zhou
Shanghai Institute of Organic Chemistry
Chen‐Xu Liu
Shanghai Institute of Organic Chemistry
Angewandte Chemie International Edition
University of Chinese Academy of Sciences
Shanghai Institute of Organic Chemistry
University of Shanghai for Science and Technology
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Yin et al. (Thu,) studied this question.
synapsesocial.com/papers/69d99fef9a6164e50fa3d1a2 — DOI: https://doi.org/10.1002/anie.202305067