Sulphones in Organic Synthesis
- 1st Edition, Volume 10 - January 28, 1993
- Latest edition
- Author: N S. Simpkins
- Editor: Patrick Perlmutter
- Language: English
Over the last twenty years the use of sulphones in organic synthesis has increased dramatically, the synthetic repertoire of sulphones having been developed to such an extent as to… Read more
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Description
Description
Over the last twenty years the use of sulphones in organic synthesis has increased dramatically, the synthetic repertoire of sulphones having been developed to such an extent as to rival the carbonyl functionality for versatility. Not only have sulphones been employed in a great many synthetic methodologies, enabling the preparation of a vast array of functionalised products, but the sulphone group has also proved to be of enormous value in many of the most demanding and sophisticated total syntheses carried out in recent years. This book describes in detail all of the important sulphone chemistry employed in organic synthesis, ranging from the well-established sulphone-mediated methods to less familiar sulphone reactions and very recent discoveries of synthetic potential.
Readership
Readership
For undergraduate and postgraduate courses in organic chemistry.
Table of contents
Table of contents
Chapter and selected section headings: Introduction to Sulphone Chemistry. The Preparation of Sulphones. Simple Alkyl Aryl and Dialkyl Sulphones. Oxidation of sulphides. Vinyl Sulphones. Ionic and radical additions to alkenes, alkynes and allenes. Allylic, Allenic, Alkynyl and Aryl Sulphones. Palladium-catalysed synthesis of allylic sulphones. Functionalised Sulphones. Hydroxy and alkoxy sulphones. Sulphonyl Carbanions. Introduction to Sulphonyl Carbanions. The structure of sulphonyl carbanions. Reactions of Simple Sulphonyl Carbanions. Alkylations. Reaction with epoxides. Reactions of Additionally Stabilised Sulphonyl Carbanions. Ketosulphones and related systems. Sulphonyl Polyanions. Polyanions from simple sulphones. Additions to Unsaturated Sulphones. Heteroatom Nucleophiles. Nitrogen nucleophiles. Non-Stabilised Organometallics. Enolates, Related Anions and Miscellaneous Carbon Nucleophiles. Cyclopropanations. Radical Additions. Rearrangements of Sulphones. Ring Expansions and Fragmentations. Sulphinate to Sulphone Rearrangements. 1,3-Rearrangements of Allylic Sulphones. The Truce-Smiles Rearrangement. Miscellaneous Rearrangements. Cycloaddition Chemistry of Unsaturated Sulphones. [2+2] Cycloadditions. [3+2] Cycloadditions. [4+2] Cycloadditions. Carbon-Carbon Double-Bond Formation by Sulphone Elimination. The Julia Olefination Reaction. Alternative beta-Eliminations of Sulphones. The Ramberg-Bäcklund Reaction. Chemistry of Cyclic Sulphones. Three-Membered Ring Sulphones. Four-Membered Ring Sulphones. Five-Membered Ring Sulphones. Functionalised Normal-Sized Rings. Larger Ring Sulphones. Desulphonylation. Simple Alkyl Aryl and Dialkyl Sulphones. Allylic Sulphones. Vinyl Sulphones. Functionalised Sulphones. Sulphone Reduction. Index.
Product details
Product details
- Edition: 1
- Latest edition
- Volume: 10
- Published: January 28, 1993
- Language: English
About the editor
About the editor
PP
Patrick Perlmutter
Patrick Perlmutter is Adjunct Professor of Chemistry at La Trobe University in Australia. He has been a university academic for 35 years with a highly active research group specialising in synthesis and new synthetic methods including conjugate additions, catalysis, total synthesis, medicinal chemistry and chemical biology. His research group has generated approximately 200 peer-reviewed publications in that time.
Affiliations and expertise
Adjunct Professor of Chemistry
La Trobe University, AustraliaAbout the author
About the author
NS
N S. Simpkins
Affiliations and expertise
Department of Chemistry, University of Nottingham, UKView book on ScienceDirect
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