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Catalytic Enantioselective Friedel-Crafts Reactions of Naphthols and Electron-Rich Phenols

Journal

SYNTHESIS-STUTTGART
Volume 48, Issue 14, Pages 2151-2164

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0035-1561434

Keywords

Friedel-Crafts reactions; asymmetric catalysis; hydroxyarenes; ketones; imines; nitroalkenes; unsaturated carbonyl compounds; allylation

Funding

  1. MINECO (Gobierno de Espana) [CTQ2013-47494-P]
  2. Generalitat Valenciana [ISIC2012/001]
  3. Universitat de Valencia

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The enantioselective Friedel-Crafts reaction is a powerful tool for the construction of benzylic stereocenters in a stereodefined manner. Significant advances have already been achieved with heteroarenes such as indoles and pyrroles; however, the reaction with homoarenes is less developed. This short review covers the most relevant literature on enantioselective Friedel-Crafts reactions with naphthols and phenols. 1 Introduction 2 Friedel-Crafts Reactions Involving 1,2-Nucleophilic Addition to C=X Bonds 3 Friedel-Crafts Reactions Involving Conjugate Nucleophilic Addition to Electrophilic C=C Bonds 4 Friedel-Crafts Reactions Involving -Allylic Complexes as Electrophiles 5 ipso-Friedel-Crafts Reactions 6 Conclusions

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