Effective and practical experimental procedures can be implemented quickly and easily in the lab. // The content of this e-book was originally published in November 2005. 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.

Auteur
Snieckus, Majewski, Trost

Résumé

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

Contenu

8.1 Product Class 1: Lithium Compounds
8.1.1 Product Subclass 1: Lithium Metal
8.1.2 Product Subclass 2: Lithium Hydride
8.1.3 Product Subclass 3: Lithium Halides, Lithium Cyanide, and Related Salts
8.1.4 Product Subclass 4: Lithium–Oxygen Compounds
8.1.5 Product Subclass 5: Lithium–Sulfur, –Selenium, and –Tellurium Compounds
8.1.6 Product Subclass 6: Lithium Amides
8.1.7 Product Subclass 7: Alkyllithium and Cycloalkyllithium Compounds
8.1.8 Product Subclass 8: Alkenyllithium Compounds
8.1.9 Product Subclass 9: Allenyllithium Compounds
8.1.10 Product Subclass 10: Lithium Acetylides
8.1.11 Product Subclass 11: Lithium Alkynolates, Alkynethiolates, and Alkyneselenolates
8.1.12 Product Subclass 12: Allyllithium Compounds
8.1.13 Product Subclass 13: Benzyllithium Compounds and (Lithiomethyl)hetarenes
8.1.14 Product Subclass 14: Aryllithium and Hetaryllithium Compounds
8.1.15 Product Subclass 15: α-Lithiocarboxylic Acids and Related Lithium Compounds (Including Enolates)
8.1.16 Product Subclass 16: β-Lithiocarboxylic Acids and Related Lithium Compounds
8.1.17 Product Subclass 17: α-Lithio Aldehydes, α-Lithio Ketones, and Related Compounds
8.1.18 Product Subclass 18: β-Lithio Aldehydes, β-Lithio Ketones, and Related Compounds
8.1.19 Product Subclass 19: sp3-Hybridized α-Lithio Ethers and O-Carbamates
8.1.20 Product Subclass 20: α-Lithio Sulfoxides
8.1.21 Product Subclass 21: α-Lithioamines
8.1.22 Product Subclass 22: Lithium Nitronates
8.1.23 Product Subclass 23: γ-Lithio Ethers and Related Compounds
8.1.24 Product Subclass 24: Carbamoyllithium and Trihalomethyllithium Compounds
8.1.25 Product Subclass 25: Tris(organosulfanyl)- and Tris(organoselanyl)methyllithium Compounds
8.1.26 Product Subclass 26: Bis(organosulfanyl)- and Bis(organoselanyl)methyllithium Compounds
8.1.27 Product Subclass 27: α-Lithio Vinyl Ethers