Affiliation:
1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences Chinese Academy of Sciences 345 Lingling Lu Shanghai 200032 China
2. School of Material and Chemistry University of Shanghai for Science and Technology Shanghai 200093 China
Abstract
AbstractEnantioselective 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.
Funder
Ministry of Science and Technology of the People's Republic of China
National Natural Science Foundation of China
Subject
General Chemistry,Catalysis
Cited by
52 articles.
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