Schaumann / Bellus / Braun Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 35

Chlorine, Bromine, and Iodine
1. Auflage 2014
ISBN: 978-3-13-172121-1
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 850 Seiten, PDF, Format (B × H): 170 mm x 240 mm

Reihe: Science of Synthesis

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
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- Discusses relevant background information and provides detailed experimental procedures

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Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Bellus, Daniel

Braun, Manfred

Freysoldt, Tonia

Göttlich, Richard

Hartung, Jens

Härtinger, Monica

Ste,

Schaumann, Ernst

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

35.1 Product Class 1: One Saturated Carbon—Chlorine Bond35.1.1 Product Subclass 1: Chloroalkanes35.1.1.1 Synthesis by Substitution of Hydrogen35.1.1.2 Synthesis by Substitution of Metals35.1.1.3 Synthesis by Substitution of Carbon Functionalities35.1.1.4 Synthesis by Substitution of Other Halogens35.1.1.5 Synthesis by Substitution of Oxygen Functionalities35.1.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities35.1.1.7 Synthesis by Substitution of Nitrogen Functionalities35.1.1.8 Synthesis by Addition to p-Type C—C Bonds35.1.1.9 Synthesis from Other Chlorine Compounds35.1.2 Product Subclass 2: Propargylic Chlorides35.1.3 Product Subclass 3: Benzylic Chlorides35.1.3.1 Synthesis by Substitution of Hydrogen35.1.3.2 Synthesis by Substitution of Carbonyl Oxygen35.1.3.3 Synthesis by Substitution of s-Bonded Heteroatoms35.1.4 Product Subclass 4: Allylic Chlorides35.1.4.1 Synthesis by Substitution of Hydrogen a to a C=C Bond35.1.4.2 Synthesis by Substitution of s-Bonded Heteroatoms35.1.5 Product Subclass 5: 1-Chloro-n-Heteroatom-Functionalized Alkanes (n =2) with Both Functions Formed Simultaneously35.1.5.1 Synthesis by Addition across C=C Bonds35.1.5.2 Synthesis by Addition across C—O Bonds35.1.5.3 Synthesis by Addition across C—S Bonds35.1.5.4 Synthesis by Addition across C—N Bonds35.1.5.5 Synthesis by Addition across C—C Bonds35.2 Product Class 2: One Saturated Carbon—Bromine Bond35.2.1 Product Subclass 1: Bromoalkanes35.2.1.1 Synthesis by Substitution of Hydrogen35.2.1.2 Synthesis by Substitution of Metals35.2.1.3 Substitution of Carbon Functionalities35.2.1.4 Synthesis by Substitution of Other Halogens35.2.1.5 Synthesis by Substitution of Oxygen Functionalities35.2.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities35.2.1.7 Synthesis by Substitution of Nitrogen Functionalities35.2.1.8 Synthesis by Addition to p-Type C—C Bonds35.2.1.9 Synthesis from Other Bromo Compounds35.2.2 Product Subclass 2: Propargylic Bromides35.2.3 Product Subclass 3: Benzylic Bromides35.2.3.1 Synthesis by Substitution of Hydrogen35.2.3.2 Synthesis by Substitution of Carbonyl Oxygen35.2.3.3 Synthesis by Substitution of s-Bonded Heteroatoms35.2.4 Product Subclass 4: Allylic Bromides35.2.4.1 Synthesis by Substitution of Hydrogen a to a C=C Bond35.2.4.2 Synthesis by Substitution of s-Bonded Heteroatoms35.2.5 Product Subclass 5: 1-Bromo-n-Heteroatom-Functionalized Alkanes (n =2) with Both Functions Formed Simultaneously35.2.5.1 Synthesis by Addition across C=C Bonds35.2.5.2 Synthesis by Addition across C—O Bonds35.2.5.3 Synthesis by Addition across C—S Bonds35.2.5.4 Synthesis by Addition across C—N Bonds35.2.5.5 Synthesis by Addition across C—C Bonds35.3 Product Class 3: One Saturated Carbon—Iodine Bond35.3.1 Product Subclass 1: Iodoalkanes35.3.1.1 Synthesis by Substitution of Hydrogen35.3.1.2 Synthesis by Substitution of Metals35.3.1.3 Synthesis by Substitution of Carbon Functionalities35.3.1.4 Synthesis by Substitution of Other Halogens35.3.1.5 Synthesis by Substitution of Oxygen Functionalities35.3.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities35.3.1.7 Synthesis by Substitution of Nitrogen Functionalities35.3.1.8 Synthesis by Addition to p-Type C—C Bonds35.3.1.9 Synthesis from Other Iodo Compounds35.3.2 Product Subclass 2: Propargylic Iodides35.3.3 Product Subclass 3: Benzylic Iodides35.3.3.1 Synthesis by Substitution of Carbonyl Oxygen35.3.3.2 Substitution of s-Bonded Heteroatoms35.3.4 Product Subclass 4: Allylic Iodides35.3.5 Product Subclass 5: 1-Iodo-n-Heteroatom-Functionalized Alkanes (n =2) with Both Functions Formed Simultaneously35.3.5.1 Synthesis by Addition across C=C Bonds35.3.5.2 Synthesis by Addition across C—O Bonds35.3.5.3 Synthesis by Addition across C—S Bonds35.3.5.4 Synthesis by Addition across C—N Bonds35.3.5.5 Synthesis by Addition across C—C Bonds

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Houben-Weyl