Pd‐Catalyzed Asymmetric Intramolecular Arylative Dearomatization of para ‐Aminophenols †
Author:
Affiliation:
1. State Key Laboratory of Organometallic ChemistryCenter for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences 345 Lingling Lu Shanghai 200032 China
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202000109
Reference120 articles.
1. For recent reviews on dearomatization reactions: (a) Pape A. R.; Kaliappan K. P.; Kündig E. P. Transition‐Metal‐Mediated Dearomatization Reactions.Chem. Rev.2000 100 2917–2940;
2. Oxidative Dearomatization of Phenols: Why, How and What For?
3. Hypervalent iodine-mediated phenol dearomatization in natural product synthesis
4. Dearomatization Strategies in the Synthesis of Complex Natural Products
5. Catalytic Asymmetric Dearomatization Reactions
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