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Inhaltsverzeichnis
1 Carbohydrates. - 1. 1 Introduction. - 1. 2 Recent developments in O-glycosidation methodology. - 1. 3 Recent developments in C-glycoside synthesis. - 1. 4 Synthesis of antibiotic sugars. - 1. 5 Use of carbohydrates as chiral templates and reagents for asymmetric synthesis. - 1. 6 Use of carbohydrates as chiral starting materials for the synthesis of enantiomerically pure natural products. - References. - 2 Aromatic compounds. - 2. 1 Introduction. - 2. 2 Benzenoids. - 2. 3 Coumarins. - 2. 4 Isocoumarins, chromanones, chromones and cannabinoids. - 2. 5 Macrocyclic lactones. - 2. 6 Pyrones, butenolides, lignans and benzofurans. - 2. 7 Terphenyls. - 2. 8 Flavonoids. - 2. 9 Xanthones and benzophenones. - 2. 10 Naphthalenes and naphthoquinones. - 2. 11 Anthraquinones. - 2. 12 Anthracyclines. - 2. 13 Some other polycyclic antibiotics. - 2. 14 Ansamycins. - References. - 3 Terpenoids. - 3. 1 Introduction. - 3. 2 Monoterpenoids. - 3. 3 Sesquiterpenoids. - 3. 4 Diterpenoids. - 3. 5 Sesterterpenoids. - 3. 6 Triterpenoids. - 3. 7 Carotenoids. - References. - 4 Steroids. - 4. 1 Introduction. - 4. 2 Molecular rearrangement. - 4. 3 Remote functionalisation. - 4. 4 Photochemical reactions. - 4. 5 Partial synthesis. - References. - 5 Amino acids, peptides and proteins. - 5. 1 Introduction. - 5. 2 Amino acids. - 5. 3 Peptides. - 5. 4 Techniques for structural elucidation. - 5. 5 Proteins. - 5. 6 Appendix. - References. - 6 Alkaloids. - 6. 1 Introduction. - 6. 2 Biomimetic studies. - 6. 3 Synthesis. - 6. 4 Marine alkaloids. - References. - 7 Nucleosides, nucleotides and nucleic acids. - 7. 1 Introduction. - 7. 2 Nucleosides. - 7. 3 Nucleotides. - 7. 4 Nucleic acids. - 7. 5 Supplementary reading. - References. - 8 Porphyrins. - 8. 1 General introduction. - 8. 2 Macrocycle biosynthesis. - 8. 3 Haemoprotein model compounds. - 8. 4 Porphyrins with easily oxidisable substituents. - 8. 5 Utilisation of porphyrin excited states. - 8. 6 Porphyrins in photodynamic therapy. - 8. 7 DNA-porphyrin interactions. - 8. 8 Porphyrins as novel materials. - 8. 9 Porphyrins with liquid crystalline properties. - References. - 9 Aliphatic compounds. - 9. 1 Introduction. - 9. 2 Semiochemicals. - 9. 3 Development of synthetic technology. - 9. 4 Marine natural products. - 9. 5 Enyne-allene and enediyne antibiotics. - References. - Chemical abbreviations and acronyms.
