Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 20b (eBook, ePUB)

Three Carbon-Heteroatom Bonds: Esters, and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te

• Format: ePub

Produktbeschreibung

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 October 2006.

Produktdetails

• Verlag: Thieme
• Seitenzahl: 1165
• Erscheinungstermin: 14. Mai 2014
• Englisch
• ISBN-13: 9783131781314
• Artikelnr.: 40845166

Autorenporträt

Science of Synthesis

Inhaltsangabe

<p>20.5 Product Class 5: Carboxylic Acid Esters<br>20.5.1 Product Subclass 1: Alkyl Alkanoates<br>20.5.1.1 Synthesis from Carbonic Acid Derivatives<br>20.5.1.2 Synthesis from Carboxylic Acids and Derivatives<br>20.5.1.3 Synthesis from Aldehydes, Ketones, and Derivatives (Including Enol Ethers)<br>20.5.1.4 Synthesis from Organometallic Compounds, Alkyl Halides, Primary Alcohols, or Ethers (Excluding Reactions with Carboxylic Acid Derivatives)<br>20.5.1.5 Synthesis from Alkenes (Excluding Reactions with Carboxylic Acid Derivatives)<br>20.5.1.6 Synthesis by Rearrangement<br>20.5.1.7 Synthesis with Retention of the Functional Group<br>20.5.2 Product Subclass 2: Arenedicarboxylic Acid Esters<br>20.5.3 Product Subclass 3: Butenedioic and Butynedioic Acid Esters<br>20.5.4 Product Subclass 4: Alkanedioic Acid Esters<br>20.5.5 Product Subclass 5: Alkynyl Alkanoates<br>20.5.6 Product Subclass 6: Aryl Alkanoates<br>20.5.7 Product Subclass 7: Alkenyl Alkanoates<br>20.5.8 Product Subclass 8: 2-Oxo- and 2-Imino-Substituted Alkanoic Acid Esters, and Related Compounds<br>20.5.9 Product Subclass 9: 2,2-Diheteroatom-Substituted Alkanoic Acid Esters<br>20.5.10 Product Subclass 10: 2-Aminoalkanoic Acid Esters (&alpha;-Amino Acid Esters)<br>20.5.11 Product Subclass 11: 2-Heteroatom-Substituted Alkanoic Acid Esters<br>20.5.12 Product Subclass 12: Alk-2-ynoic Acid Esters<br>20.5.13 Product Subclass 13: Arenecarboxylic Acid Esters<br>20.5.14 Product Subclass 14: Alk-2-enoic Acid Esters<br>20.5.15 Product Subclass 15: 3-Oxo- and 3,3-Diheteroatom-Substituted Alkanoic Acid Esters<br>20.5.16 Product Subclass 16: 3-Heteroatom-Substituted Alkanoic Acid Esters<br>20.6 Product Class 6: Lactones<br>20.7 Product Class 7: Peroxy Acids and Derivatives<br>20.8 Product Class 8: Thiocarboxylic <em>S</em>-Acids, Selenocarboxylic <em>Se</em>-Acids, Tellurocarboxylic <em>Te</em>-Acids, and Derivatives</p>