Heterocyclic Chemistry, 5th Edition
Table of Contents
Definitions of abbreviations
1. Heterocyclic nomenclature
2. Structures and spectroscopic properties of aromatic heterocycles
3. Substitutions of aromatic heterocycles
4. Organometallic heterocyclic chemistry
5. Methods in heterocyclic chemistry
6. Ring synthesis of aromatic heterocycles
7. Typical reactivity of pyridines, quinolines and isoquinolines
8. Pyridines: reactions and synthesis
9. Quinolines and isoquinolines: reactions and synthesis
10. Typical reactivity of pyrylium and benzopyrylium ions, pyrones and benzopyrones
11. Pyryliums, 2- and 4-pyrones: reactions and synthesis
12. Benzopyryliums, benzopyrones: reactions and synthesis
13. Typical reactivity of the diazines: pyridazine, pyrimidine and pyrazine
14. The diazines: pyridazine, pyrimidine, and pyrazine: reactions and synthesis
15. Typical reactivity of pyrroles, thiophenes, and furans
16. Pyrroles: reactions and synthesis
17. Thiophenes: reactions and synthesis
18. Furans: reactions and synthesis
19. Typical reactivity of indoles, benzo[b]thiophenes, benzo[b]furans, isoindoles, benzo[c]thiophenes and isobenzofurans
20. Indoles: reactions and synthesis
21. Benzo[b]thiophenes and benzo[b]furans: reactions and synthesis
22. Isoindoles, benzo[c]thiophenes and isobenzofurans: reactions and synthesis
23. Typical reactivity of 1,3- and 1,2-azoles and benzo-1,3- and -1,2-azoles
24. 1,3-Azoles: imidazoles, thiazoles, and oxazoles: reactions and synthesis
25. 1,2-Azoles: pyrazoles, isothiazoles, isoxazoles: reactions and synthesis
26. Benzanellated azoles: reactions and synthesis
27. Purines: reactions and synthesis
28. Heterocycles containing a ring-junction nitrogen (bridgehead compounds)
29. Heterocycles containing more than two heteroatoms
30. Saturated and partially unsaturated heterocyclic compounds: reactions and synthesis
31. Special topics
32. Heterocycles in biochemistry; heterocyclic natural products
33. Heterocycles in medicine