Section 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
Section B: Making Carbon-Carbon Bonds
7. The Ortho Strategy for Aromatic Compounds
8. s-Complexes of Metals
9. Controlling the Michael Reaction
10. Specific Enol Equivalents
11. Extended Enolates
12. Allyl Anions
13. Homoenolates
14. Acyl Anion Equivalents
Section C: Carbon-Carbon Double Bonds
15. Synthesis of Double Bonds of Defined Stereochemistry
16. Vinyl Anions
17. Electrophilic Attack on Alkenes
18. Vinyl Cations
19. Allyl Alcohols: Allyl Cation Equivalents (and More)
Section D: Stereochemistry
20. Control of Stereochemistry -- Introduction
21. Diastereoselectivity
22. Resolution
23. The Chiral Pool: Asymmetric Synthesis with Natural Products as Starting Materials
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: Enantiomerically Pure Compounds & Sophisticated Syntheses
31. Strategy of Asymmetric Synthesis
Section E: Functional Group Strategy
32. Functionalisation of Pyridine
33. Oxidation of Aromatic Rings and of Enol(ate)s
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
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