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

Science of Synthesis provides a critical review of the synthetic methodology developed from the early 1800s to date for the entire field of organic and organometallic chemistry. As the only resource providing full-text descriptions of organic transformations and synthetic methods as well as experimental procedures, Science of Synthesis is therefore a unique chemical information tool. Over 1000 world-renowned experts have chosen the most important molecular transformations for a class of organic compounds and elaborated on their scope and limitations. The systematic, logical and consistent organization of the synthetic methods for each functional group enables users to quickly find out which methods are useful for a particular synthesis and which are not. Effective and practical experimental procedures can be implemented quickly and easily in the lab.// The content of this e-book was originally published in December 2006.

Autorentext
Houben-Weyl

Zusammenfassung
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

Inhalt
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 π-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 σ-Bonded Heteroatoms
35.1.4 Product Subclass 4: Allylic Chlorides
35.1.4.1 Synthesis by Substitution of Hydrogen α to a C=C Bond
35.1.4.2 Synthesis by Substitution of σ-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 π-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 σ-Bonded Heteroatoms
35.2.4 Product Subclass 4: Allylic Bromides
35.2.4.1 Synthesis by Substitution of Hydrogen α to a C=C Bond
35.2.4.2 Synthesis by Substitution of σ-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...

#	Onlineshop	Preis CHF	Versand CHF	Total CHF
1	Seller	0.00	0.00	0.00