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

Chlorine, Bromine, and Iodine
1. Auflage 2014
ISBN: 978-3-13-178311-0
Verlag: Thieme
Format: EPUB
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 850 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.

Schaumann, Ernst

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

35.1 Product Class 1: One Saturated Carbon—Chlorine Bond
35.1.1 Product Subclass 1: Chloroalkanes
35.1.1.1 Synthesis by Substitution of Hydrogen
35.1.1.2 Synthesis by Substitution of Metals
35.1.1.3 Synthesis by Substitution of Carbon Functionalities
35.1.1.4 Synthesis by Substitution of Other Halogens
35.1.1.5 Synthesis by Substitution of Oxygen Functionalities
35.1.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities
35.1.1.7 Synthesis by Substitution of Nitrogen Functionalities
35.1.1.8 Synthesis by Addition to p-Type C—C Bonds
35.1.1.9 Synthesis from Other Chlorine Compounds
35.1.2 Product Subclass 2: Propargylic Chlorides
35.1.3 Product Subclass 3: Benzylic Chlorides
35.1.3.1 Synthesis by Substitution of Hydrogen
35.1.3.2 Synthesis by Substitution of Carbonyl Oxygen
35.1.3.3 Synthesis by Substitution of s-Bonded Heteroatoms
35.1.4 Product Subclass 4: Allylic Chlorides
35.1.4.1 Synthesis by Substitution of Hydrogen a to a C=C Bond
35.1.4.2 Synthesis by Substitution of s-Bonded Heteroatoms
35.1.5 Product Subclass 5: 1-Chloro-n-Heteroatom-Functionalized Alkanes (n =2) with Both Functions Formed Simultaneously
35.1.5.1 Synthesis by Addition across C=C Bonds
35.1.5.2 Synthesis by Addition across C—O Bonds
35.1.5.3 Synthesis by Addition across C—S Bonds
35.1.5.4 Synthesis by Addition across C—N Bonds
35.1.5.5 Synthesis by Addition across C—C Bonds
35.2 Product Class 2: One Saturated Carbon—Bromine Bond
35.2.1 Product Subclass 1: Bromoalkanes
35.2.1.1 Synthesis by Substitution of Hydrogen
35.2.1.2 Synthesis by Substitution of Metals
35.2.1.3 Substitution of Carbon Functionalities
35.2.1.4 Synthesis by Substitution of Other Halogens
35.2.1.5 Synthesis by Substitution of Oxygen Functionalities
35.2.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities
35.2.1.7 Synthesis by Substitution of Nitrogen Functionalities
35.2.1.8 Synthesis by Addition to p-Type C—C Bonds
35.2.1.9 Synthesis from Other Bromo Compounds
35.2.2 Product Subclass 2: Propargylic Bromides
35.2.3 Product Subclass 3: Benzylic Bromides
35.2.3.1 Synthesis by Substitution of Hydrogen
35.2.3.2 Synthesis by Substitution of Carbonyl Oxygen
35.2.3.3 Synthesis by Substitution of s-Bonded Heteroatoms
35.2.4 Product Subclass 4: Allylic Bromides
35.2.4.1 Synthesis by Substitution of Hydrogen a to a C=C Bond
35.2.4.2 Synthesis by Substitution of s-Bonded Heteroatoms
35.2.5 Product Subclass 5: 1-Bromo-n-Heteroatom-Functionalized Alkanes (n =2) with Both Functions Formed Simultaneously
35.2.5.1 Synthesis by Addition across C=C Bonds
35.2.5.2 Synthesis by Addition across C—O Bonds
35.2.5.3 Synthesis by Addition across C—S Bonds
35.2.5.4 Synthesis by Addition across C—N Bonds
35.2.5.5 Synthesis by Addition across C—C Bonds
35.3 Product Class 3: One Saturated Carbon—Iodine Bond
35.3.1 Product Subclass 1: Iodoalkanes
35.3.1.1 Synthesis by Substitution of Hydrogen
35.3.1.2 Synthesis by Substitution of Metals
35.3.1.3 Synthesis by Substitution of Carbon Functionalities
35.3.1.4 Synthesis by Substitution of Other Halogens
35.3.1.5 Synthesis by Substitution of Oxygen Functionalities
35.3.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities
35.3.1.7 Synthesis by Substitution of Nitrogen Functionalities
35.3.1.8 Synthesis by Addition to p-Type C—C Bonds
35.3.1.9 Synthesis from Other Iodo Compounds
35.3.2 Product Subclass 2: Propargylic Iodides
35.3.3 Product Subclass 3: Benzylic Iodides
35.3.3.1 Synthesis by Substitution of Carbonyl Oxygen
35.3.3.2 Substitution of s-Bonded Heteroatoms
35.3.4 Product Subclass 4: Allylic Iodides
35.3.5 Product Subclass 5: 1-Iodo-n-Heteroatom-Functionalized Alkanes (n =2) with Both Functions Formed Simultaneously
35.3.5.1 Synthesis by Addition across C=C Bonds
35.3.5.2 Synthesis by Addition across C—O Bonds
35.3.5.3 Synthesis by Addition across C—S Bonds
35.3.5.4 Synthesis by Addition across C—N Bonds
35.3.5.5 Synthesis by Addition across C—C Bonds

Über Autor(innen)

Houben-Weyl