Beschreibung:
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 ...
Turning Information into Knowledge
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 Series Editors: D. Bellus, S. V. Ley, R. Noyori, M. Regitz, E. Schaumann, I. Shinkai, E. J. Thomas, B. M. Trost, P. J. Reider.
<p>26.1 Product Class 1: Aliphatic and Alicyclic Ketones (Excluding Cyclobutanones and Cyclopropanones)<br>26.1.1 Synthesis by Oxidation of Heterosubstituted Alkanes<br>26.1.2 Synthesis by Oxidation of Alkenes and Alkanes (Excluding Allylic or Benzylic Derivatives)<br>26.1.3 Synthesis by Reduction of 1,2-Diketones and α-Diazo Ketones, α,α-Dihetero- and α-Heterosubstituted Ketones, Enones, and Ynones<br>26.1.4 Synthesis from Carboxylic Acids and Derivatives by Substitution with a Carbon Nucleophile<br>26.1.5 Synthesis from Aldehydes by Substitution of the Aldehyde Hydrogen<br>26.1.6 Synthesis from Thioketones, Acetals, Cyanohydrins, Enol Ethers, Enamines, Other Ene Derivatives, and Related Compounds<br>26.1.7 Synthesis by Addition<br>26.1.8 Synthesis by Fragmentation and Rearrangement<br>26.1.9 Synthesis from Other Ketones<br>26.1.10 Synthesis from Enones by Formation of C—C Bonds<br>26.2 Product Class 2: Cyclobutanones and Their Precursors<br>26.3 Product Class 3: Cyclopropanones and Their Precursors<br>26.4 Product Class 4: 1,2-Diketones and Related Compounds<br>26.5 Product Class 5: α,α-Diheterosubstituted Ketones<br>26.6 Product Class 6: α-Heterosubstituted Ketones<br>26.7 Product Class 7: Ynones<br>26.8 Product Class 8: Aryl Ketones<br>26.9 Product Class 9: Enones<br>26.10 Product Class 10: Saturated or Unsaturated Ketones with an Additional Carbonyl, Nitrile, or Carboxy Substituent or Equivalent at a β or More Remote Position: Synthesis of the Ketone Functionality<br>26.11 Product Class 11: Saturated and Unsaturated Ketones Containing a β- or More Remote Heteroatom Substituent</p>
