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Direct Asymmetric Dearomatization of 2‐Naphthols by Scandium‐Catalyzed Electrophilic Amination
Authors:Jiang Nan  Prof. Dr. Jingjing Liu  Huayu Zheng  Zhijun Zuo  Prof. Dr. Lei Hou  Prof. Dr. Huaiming Hu  Prof. Dr. Yaoyu Wang  Prof. Dr. Xinjun Luan
Affiliation:Key Laboratory of Synthetic and Natural Functional Molecular Chemistry of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 (China)
Abstract:Catalytic asymmetric aminative dearomatization of 1‐substituted 2‐naphthols was successfully implemented with electrophilic azodicarboxylates under the catalysis of chiral ScIII/pybox complexes. This intermolecular reaction represents a hitherto unknown enantioselective C? N bond‐forming process through direct dearomatization of phenolic compounds to generate chiral nitrogen‐containing quaternary carbon stereocenters.
Keywords:amination  asymmetric catalysis  dearomatization  naphthol  scandium
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