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

Arene-X (X=Hal, O, S, Se, Te)
Science of Synthesis 1. Auflage

von: Christopher A. Ramsden
2.399,99 €
Verlag:	Thieme
Format:	PDF
Veröffentl.:	14.05.2014
ISBN/EAN:	9783131720610
Sprache:	englisch
Anzahl Seiten:	1312

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Titelbeschreibung

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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.
<UL><LI>Contains the expertise of presently 400 leading
chemists worldwide

<LI>Critically evaluates the preparative applicability
and significance of the synthetic methods

<LI>Discusses relevant background information and provides detailed experimental procedures</LI></UL>
For full information on the Science of Synthesis series, visit the Science of Synthesis Homepage</BODY></HTML>

Inhaltsverzeichnis

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