Chapter 6. Synthesis of Phenols

  1. Zvi Rappoport
  1. Concepción González1 and
  2. Luis Castedo2

Published Online: 7 OCT 2003

DOI: 10.1002/0470857277.ch6

Phenols

Phenols

How to Cite

González, C. and Castedo, L. (2003) Synthesis of Phenols, in Phenols (ed Z. Rappoport), John Wiley & Sons, Ltd, Chichester, UK. doi: 10.1002/0470857277.ch6

Editor Information

  1. The Hebrew University, Jerusalem, Israel

Author Information

  1. 1

    Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Santiago de Compostela, 27002 Lugo, Spain. Fax: +34 982 22 49 04

  2. 2

    Departamento de Química Orgánica y Unidad Asociada al C.S.I.C., Facultad de Química, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain. Fax: +34 981 59 50 12

Publication History

  1. Published Online: 7 OCT 2003
  2. Published Print: 22 JUL 2003

Book Series:

  1. PATAI'S Chemistry of Functional Groups

Book Series Editors:

  1. Zvi Rappoport

Series Editor Information

  1. The Hebrew University, Jerusalem, Israel

ISBN Information

Print ISBN: 9780471497370

Online ISBN: 9780470857274

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Summary

This chapter contains sections titled:

  • By Displacement of Other Functional Groups

    • From Aryl Halides

    • From Sulphonic Acids

    • From Nitrogen Derivatives

      • Hydrolysis

      • Bucherer Reaction

      • Diazotation Reaction

  • By Oxidation

    • Hydroxylation

      • With Hydrogen Peroxide

      • With Peroxides

      • With Peroxyacids

        • Inorganic Peroxyacids

        • Organic Peroxyacids

      • Electrochemical Hydroxylation

      • Biotransformations

      • Miscellaneous Methods

    • Oxidation of Organometallic Derivatives

    • Oxidation of Nitrogen Derivatives

    • Oxidation of Carbonyl Groups

  • By Condensation

    • Cyclization

    • Claisen and Aldolic Condensations

      • Intramolecular Reaction

      • Intermolecular Reaction

        • Synthesis of Monophenols

        • Synthesis of Resorcinols

    • Radical Cyclizations

  • By Cycloaddition

    • Cycloaromatization

    • Diels–Alder Reaction

    • Benzannulation

  • By Rearrangement

    • Alkyl and Benzyl Aryl Ethers

    • Allyl Aryl Ethers. Aromatic Claisen Rearrangement

    • Diaryl Ethers. Smiles Rearrangement

    • Dienones. Dienone–Phenol Rearrangement

    • Phenolic Esters. Fries Rearrangement

  • Acknowledgement

  • References