Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 31a (eBook, ePUB)

Arene-X (X=Hal, O, S, Se, Te)

• Format: ePub

Produktbeschreibung

Science of Synthesis: Houben-Weyl Methods of Molecular Transformations is the entirely new edition of the acclaimed reference series Houben-Weyl, the standard synthetic chemistry resource since 1909. This new edition is published in English and will comprise 48 volumes published between the years 2000 and 2008.

Science of Synthesis is a quality reference work developed by a highly esteemed editorial board to provide a comprehensive and critical selection of reliable organic and organometallic synthetic methods. This unique resource is designed to be the first point of reference when searching for a synthesis strategy.

• Contains the expertise of presently 400 leading chemists worldwide
• Critically evaluates the preparative applicability and significance of the synthetic methods
• Discusses relevant background information and provides detailed experimental procedures

For full information on the Science of Synthesis series, visit the Science of Synthesis Homepage

Produktdetails

• Verlag: Thieme
• Seitenzahl: 1312
• Erscheinungstermin: 14. Mai 2014
• Englisch
• ISBN-13: 9783131782519
• Artikelnr.: 40842895

Autorenporträt

Christopher A. Ramsden

Inhaltsangabe

<p>31.1 Product Class 1: Fluoroarenes<br>31.2 Product Class 2: Chloroarenes<br>31.3 Product Class 3: Bromoarenes<br>31.4 Product Class 4: Aryl Iodine Compounds<br>31.4.1 Product Subclass 1: Hypervalent Iodoarenes and Aryliodonium Salts<br>31.4.2 Product Subclass 2: Iodoarenes<br>31.5 Product Class 5: Phenols and Phenolates<br>31.5.1 Product Subclass 1: Monohydric Phenols and Corresponding Phenolates<br>31.5.1.1 Synthesis by Substitution<br>31.5.1.2 Synthesis by Elimination<br>31.5.1.3 Synthesis by Rearrangement<br>31.5.1.4 Synthesis with Retention of the Functional Group<br>31.5.1.5 Synthesis from Nonaromatic Precursors<br>31.5.2 Product Subclass 2: Polyhydric Phenols and Corresponding Phenolates<br>31.5.2.1 Synthesis by Substitution<br>31.5.2.2 Synthesis by Elimination<br>31.5.2.3 Synthesis by Addition<br>31.5.2.4 Synthesis by Rearrangement<br>31.5.2.5 Synthesis with Retention of the Functional Group<br>31.6 Product Class 6: Aryl Ethers<br>31.6.1 Product Subclass 1: Diaryl Ethers<br>31.6.2 Product Subclass 2: Alkyl Aryl Ethers<br>31.6.2.1 Synthesis by Substitution<br>31.6.2.2 Synthesis by Elimination<br>31.6.2.3 Synthesis by Rearrangement<br>31.6.2.4 Synthesis with Retention of the Functional Group<br>31.6.2.5 Synthesis from Nonaromatic Precursors<br>31.7 Product Class 7: Aryl Hypohalites, Aryl Peroxides, and Aryloxy Sulfur Compounds<br>31.8 Product Class 8: Cyclic Aryl Ethers<br>31.9 Product Class 9: Arenesulfonic Acids and Derivatives<br>31.9.1 Product Subclass 1: Arenesulfonic Acids and Arenesulfonate Salts<br>31.9.2 Product Subclass 2: Arenesulfonic Acid Derivatives<br>31.10 Product Class 10: Aryl Sulfones and Nitrogen Derivatives<br>31.11 Product Class 11: Arenesulfinic Acids and Derivatives<br>31.12 Product Class 12: Aryl Sulfoxides and <em>S</em>-Arylsulfimides<br>31.13 Product Class 13: Arenethiols and Arenethiolates<br>31.14 Product Class 14: Aryl Sulfides<br>31.15 Product Class 15: Arylsulfonium Salts and Derivatives<br>31.16 Product Class 16: Arenesulfenic Acids and Derivatives<br>31.17 Product Class 17: Aryl Polysulfides<br>31.18 Product Class 18: Cyclic Aryl Sulfides<br>31.19 Product Class 19: Aryl Selenium Compounds<br>31.20 Product Class 20: Aryl Tellurium Compounds</p>