Panek / Beignet / Bellus Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 20b

Three Carbon-Heteroatom Bonds: Esters, and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te
1. Auflage 2014
ISBN: 978-3-13-171941-6
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Deutsch, Englisch, 1165 Seiten, PDF, Format (B × H): 170 mm x 240 mm

Reihe: Science of Synthesis

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.

Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Beignet, Julien

Bellus, Daniel

Evano, Gwilherm

Garbacci, Robert

Panek, James

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

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

Über Autor(innen)

Science of Synthesis