Ramsden Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 31a

Arene-X (X=Hal, O, S, Se, Te)
1. Auflage 2014
ISBN: 978-3-13-178251-9
Verlag: Thieme
Format: EPUB
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 1312 Seiten, ePub, Format (B × H): 170 mm x 240 mm

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

Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Ramsden, C. A.

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

31.1 Product Class 1: Fluoroarenes31.2 Product Class 2: Chloroarenes31.3 Product Class 3: Bromoarenes31.4 Product Class 4: Aryl Iodine Compounds31.4.1 Product Subclass 1: Hypervalent Iodoarenes and Aryliodonium Salts31.4.2 Product Subclass 2: Iodoarenes31.5 Product Class 5: Phenols and Phenolates31.5.1 Product Subclass 1: Monohydric Phenols and Corresponding Phenolates31.5.1.1 Synthesis by Substitution31.5.1.2 Synthesis by Elimination31.5.1.3 Synthesis by Rearrangement31.5.1.4 Synthesis with Retention of the Functional Group31.5.1.5 Synthesis from Nonaromatic Precursors31.5.2 Product Subclass 2: Polyhydric Phenols and Corresponding Phenolates31.5.2.1 Synthesis by Substitution31.5.2.2 Synthesis by Elimination31.5.2.3 Synthesis by Addition31.5.2.4 Synthesis by Rearrangement31.5.2.5 Synthesis with Retention of the Functional Group31.6 Product Class 6: Aryl Ethers31.6.1 Product Subclass 1: Diaryl Ethers31.6.2 Product Subclass 2: Alkyl Aryl Ethers31.6.2.1 Synthesis by Substitution31.6.2.2 Synthesis by Elimination31.6.2.3 Synthesis by Rearrangement31.6.2.4 Synthesis with Retention of the Functional Group31.6.2.5 Synthesis from Nonaromatic Precursors31.7 Product Class 7: Aryl Hypohalites, Aryl Peroxides, and Aryloxy Sulfur Compounds31.8 Product Class 8: Cyclic Aryl Ethers31.9 Product Class 9: Arenesulfonic Acids and Derivatives31.9.1 Product Subclass 1: Arenesulfonic Acids and Arenesulfonate Salts31.9.2 Product Subclass 2: Arenesulfonic Acid Derivatives31.10 Product Class 10: Aryl Sulfones and Nitrogen Derivatives31.11 Product Class 11: Arenesulfinic Acids and Derivatives31.12 Product Class 12: Aryl Sulfoxides and S-Arylsulfimides31.13 Product Class 13: Arenethiols and Arenethiolates31.14 Product Class 14: Aryl Sulfides31.15 Product Class 15: Arylsulfonium Salts and Derivatives31.16 Product Class 16: Arenesulfenic Acids and Derivatives31.17 Product Class 17: Aryl Polysulfides31.18 Product Class 18: Cyclic Aryl Sulfides31.19 Product Class 19: Aryl Selenium Compounds31.20 Product Class 20: Aryl Tellurium Compounds

Über Autor(innen)

Christopher A. Ramsden