Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 25 (eBook, PDF)

Aldehydes

• Format: PDF

Produktbeschreibung

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

Produktdetails

• Verlag: Thieme
• Seitenzahl: 902
• Erscheinungstermin: 14. Mai 2014
• Englisch
• ISBN-13: 9783131719911
• Artikelnr.: 40838415

Autorenporträt

Houben-Weyl

Inhaltsangabe

<p>25.1 Product Class 1: Aliphatic and Alicyclic Aldehydes<br>25.1.1 Synthesis by Oxidative Cleavage<br>25.1.2 Synthesis by Oxidation<br>25.1.3 Synthesis by Isomerization<br>25.1.4 Synthesis by Reduction or by Reduction Followed by Hydrolysis<br>25.1.5 Synthesis by Elimination or Rearrangement<br>25.1.6 Synthesis by Protonation<br>25.1.7 Synthesis by Hydrolysis<br>25.1.8 Synthesis by Hydration of Alkynes<br>25.1.9 Synthesis by Formylation of Enolates<br>25.1.10 Synthesis by Homologation of Aldehydes<br>25.1.11 Synthesis by Hydroformylation of Alkenes<br>25.1.12 Synthesis by C₁-Extension of Alkyl Halides<br>25.1.13 Synthesis by C₁-Extension of Organometallics<br>25.1.14 Synthesis by C₂-Elongation<br>25.1.15 Synthesis by C₃-Elongation<br>25.1.16 Synthesis by Diels&#8211;Alder Reactions with Enals or Their Acetals<br>25.2 Product Class 2: 2-Oxoaldehydes and Heteroatom Analogues<br>25.3 Product Class 3: 2,2-Diheteroatom-Substituted Aldehydes<br>25.4 Product Class 4: 2-Heteroatom-Substituted Aldehydes and Sugar Aldehydes<br>25.5 Product Class 5: Ynals<br>25.6 Product Class 6: Arenecarbaldehydes<br>25.6.1 Synthesis by Oxidative Cleavage of Carbon&#8212;Carbon Bonds<br>25.6.2 Synthesis by Oxidation<br>25.6.3 Synthesis by Reduction<br>25.6.4 Synthesis by Hydrolysis of Aldehyde Derivatives<br>25.6.5 Synthesis by Formylation of Arylmetal Reagents<br>25.6.6 Synthesis by Formylation of Arene&#8212;Hydrogen Bonds<br>25.6.7 Synthesis by Carbonylation of Arylpalladium Intermediates<br>25.6.8 Synthesis by C&#8212;C Bond Formation<br>25.6.9 Synthesis by C&#8212;X Bond Formation<br>25.7 Product Class 7: Polyenals<br>25.8 Product Class 8: &alpha;,&beta;-Unsaturated Aldehydes<br>25.9 Product Class 9: 3-Heteroatom-Substituted Aldehydes</p>