Organic Synthesis

Strategy and Control

Häftad, Engelska, 2007

Av Paul Wyatt, Stuart Warren, UK) Wyatt, Paul (School of Chemistry, University of Bristol, UK) Warren, Stuart (Department of Chemistry, University of Cambridge, Wyatt, Warren

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Organic Synthesis: Strategy and Control is a sequel to Stuart Warren's bestseller Organic Synthesis: The Disconnection Approach. The 'Disconnection' book concentrated on the planning behind the synthesis of compounds.The two themes of this new book are strategy and control: solving problems either by finding an alternative strategy or by controlling any established strategy to make it work.The book is divided into five sections that deal with selectivity, carbon-carbon single bonds, carbon-carbon double bonds, stereochemistry and functional group strategy. Interpenetrating this structure, the 36 chapters start with classic methods and progress to modern methods and modern strategic considerations. Heterocyclic chemistry is treated throughout the book with full mechanistic explanations as part of organic chemistry rather than a separate mystery. A comprehensive, practical account of the key concepts involved in synthesising compounds.Takes a mechanistic approach, which explains reactions and gives guidelines on how reactions might behave in different situations.Focuses on reactions that really work rather than those with limited application.Extensive, up-to-date references in each chapter.Students and professional chemists familiar with Organic Synthesis: The Disconnection Approach will enjoy the leap into a book designed for chemists at the coalface of organic synthesis.

Produktinformation

Utgivningsdatum2007-04-20
Mått191 x 248 x 41 mm
Vikt1 520 g
FormatHäftad
SpråkEngelska
Antal sidor928
FörlagJohn Wiley & Sons Inc
ISBN9780471929635

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Organisk kemi inom Naturvetenskap och teknik

A: Introduction: Selectivity. 1. Planning Organic Syntheses: Tactics, Strategy, and Control. 2. Chemoselectivity. 3. Regioselectivity: Controlled Aldol Reactions. 4. Stereoselectivity: Stereoselective Aldol Reactions. 5. Alternative Strategies for Enone Synthesis. 6. Choosing a Strategy : The Synthesis of cyclopentenones. B: Making Carbon-Carbon Bonds. 7. The Ortho Strategy for Aromatic Compounds. 8. ´-Complexes of Metals. 9. Controlling the Michael Reaction. 10. Specific Enol Equivalents. 11. Extended Enolates. 12. Allyl Anions. 13. Homoenolates. 14. Acyl Anion Equivalents. C: Carbon-Carbon Double Bonds. 15. Synthesis of Double Bonds of Defined Stereochemistry. 16. Stereo-Controlled Vinyl Anion Equivalents. 17. Electrophilic Attack on Alkenes. 18. Vinyl Cations: Palladium-Catalysed C-C Coupling. 19. Allyl Alcohols: Allyl Cation Equivalents (and More). D: Stereochemistry. 20. Control of Stereochemistry -- Introduction. 21 Controlling Relative Stereochemistry. 22. Resolution. 23. The Chiral Pool. 24. Asymmetric Induction I: Reagent-Based Strategy. 25. Asymmetric Induction II: Asymmetric Catalysis: Formation of C-O and C-N Bonds. 26. Asymmetric Induction III: Asymmetric Catalysis: Formation of C-H and C-C Bonds. 27. Asymmetric Induction IV: Substrate-Based Strategy. 28. Kinetic Resolution. 29. Enzymes: Biological Methods in Asymmetric Synthesis. 30. New Chiral Centres from Old. 31. Strategy of Asymmetric Synthesis. E: Functional Group Strategy. 32. Functionalisation of Pyridine. 33. Oxidation of Aromatic Compounds, Enols and Enolates. 34. Functionality and Pericyclic Reactions: Nitrogen Heterocycles by Cycloadditions and Sigmatropic Rearrangements. 35. Synthesis and Chemistry of Azoles and other Heterocycles with Two or more Heteroatoms. 36. Tandem Organic Reactions. General References. Index.

This is a book which will change the way you think about making molecules. (Chemistry World, July 2008) The authors can be commended on producing a really useful and enjoyable new book on Organic Synthesis. (Reviews, June 2008) "The authors have spent approximately ten years putting this excellent book together, and their hard work has paid off." (Journal of Chemical Education, May 2008) "Of interest to the experienced practitioner looking to broaden (or reawaken) awareness of the remarkable diversity of available synthetic transformations"(Journal of Medicinal Chemistry, 2008)