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      Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives.

      1 , 2 , 1
      Chemical Society reviews
      Royal Society of Chemistry (RSC)

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          Abstract

          Phenols are widely used as starting materials in both industrial and academic society. Dearomatization reactions of phenols provide an efficient way to construct highly functionalized cyclohexadienones. The main challenge to make them asymmetric by catalytic methods is to control the selectivity while overcoming the loss of aromaticity. In this tutorial review, an up to date summary of recent progress in CADA reactions of phenol and aniline derivatives is presented.

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          Catalytic Asymmetric Dearomatization Reactions

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            A Chiral Hypervalent Iodine(III) Reagent for Enantioselective Dearomatization of Phenols

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              Enantioselective Kita Oxidative Spirolactonization Catalyzed by In Situ Generated Chiral Hypervalent Iodine(III) Species

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                Author and article information

                Journal
                Chem Soc Rev
                Chemical Society reviews
                Royal Society of Chemistry (RSC)
                1460-4744
                0306-0012
                Mar 21 2016
                : 45
                : 6
                Affiliations
                [1 ] State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China. slyou@sioc.ac.cn.
                [2 ] Department of Chemistry & Biochemistry, University of California, Santa Barbara, California 93106, USA. zhang@chem.ucsb.edu.
                Article
                10.1039/c5cs00356c
                26796922
                024359e3-5956-40f9-8d34-72c71420f47c
                History

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