Paul Wyatt, Stuart Warren

Organic Synthesis (eBook, ePUB)

Strategy and Control

• Format: ePub

Produktbeschreibung

Organic Synthesis: Strategy and Control is the long-awaited sequel to Stuart Warren's bestseller Organic Synthesis: The Disconnection Approach, which looked at the planning behind the synthesis of compounds. This unique book now provides a comprehensive, practical account of the key concepts involved in synthesising compounds and focuses on putting the planning into practice. The two themes of the 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. * 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 * Contains 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.

---

Dieser Download kann aus rechtlichen Gründen nur mit Rechnungsadresse in A, B, BG, CY, CZ, D, DK, EW, E, FIN, F, GR, HR, H, IRL, I, LT, L, LR, M, NL, PL, P, R, S, SLO, SK ausgeliefert werden.

Produktdetails

• Verlag: John Wiley & Sons
• Seitenzahl: 920
• Erscheinungstermin: 20. Mai 2013
• Englisch
• ISBN-13: 9781118681442
• Artikelnr.: 39054552

Autorenporträt

Paul Wyatt, Senior Lecturer and Director of Undergraduate Studies, School of Chemistry, University of Bristol, UK and Stuart Warren, Reader in Organic Chemistry, Department of Chemistry, University of Cambridge, UK.

Inhaltsangabe

Preface.

A: Introduction: Selectivity.

1. Planning Organic Syntheses: Tactics, Strategy, andControl.

2. Chemoselectivity.

3. Regioselectivity: Controlled Aldol Reactions.

4. Stereoselectivity: Stereoselective AldolReactions.

5. Alternative Strategies for Enone Synthesis.

6. Choosing a Strategy : The Synthesis ofcyclopentenones.

B: Making Carbon-Carbon Bonds.

7. The Ortho Strategy for Aromatic Compounds.

8. delta-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 DefinedStereochemistry.

16. Stereo-Controlled Vinyl Anion Equivalents.

17. Electrophilic Attack on Alkenes.

18. Vinyl Cations: Palladium-Catalysed C-CCoupling.

19. Allyl Alcohols: Allyl Cation Equivalents (andMore).

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-BasedStrategy.

28. Kinetic Resolution.

29. Enzymes: Biological Methods in AsymmetricSynthesis.

30. New Chiral Centres from Old --Enantiomerically Pure Compounds & SophisticatedSyntheses.

31. Strategy of Asymmetric Synthesis.

E: Functional Group Strategy.

32. Functionalisation of Pyridine.

33. Oxidation of Aromatic Compounds, Enols andEnolates.

34. Functionality and Pericyclic Reactions: NitrogenHeterocycles by Cycloadditions and Sigmatropic Rearrangements.

35. Synthesis and Chemistry of Azoles and otherHeterocycles with Two or more Heteroatoms.

36. Tandem Organic Reactions.

General References.

Index.

Rezensionen

"The authors can be commended on producing a really useful and enjoyable new book on Organic Synthesis! ... .Rewarding to read." (The Higher Education Academy Physical Sciences Centre, June 2008)