Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products

- Naturally Occurring Isocoumarins
I. Introduction
II. Nomenclature and Structural Types
III. Structure Determination
IV. Synthesis
V. Biosynthesis
VI. Biological Activity
VII. Introduction to the Tables
- Table 1. Isocoumarins with no 8-Oxygenation
- Table 2. Isocoumarins with 8-Oxygenation
- (a) With no Carbon Substituent at C-3
- (b) With a One-Carbon Substituent at C-3
- (c) With a Substituent at C-3 Containing More than One Carbon
- Table 3. Isocoumarins with 6,8-Dioxygenation
- (a) With no Carbon Substituent at C-3
- (b) With a One-Carbon Substituent at C-3
- (c) With a Substituent at C-3 Containing More than One Carbon. 32
- Table 4. Isocoumarins with 6,7,8-Trioxygenation
- (a) With a One-Carbon Substituent at C-3
- (b) With a Substituent at C-3 Containing More than One Carbon. 39
- Table 5. Isocoumarins with Fused Carbocyclic Rings
- (a) 3,4-Fused
- (b) 4,5-Fused
- (c) 6,7-Fused
- Table 6. Isocoumarins with Nitrogen-Containing Substituents
- Formula Index
- Trivial Name Index
- Source Index
- References
- Anthraquinones in the Rubiaceae
I. Introduction
II. Biological Activity
III. Biosynthesis
IV. Spectroscopy
1. UV Spectroscopy
2. IR Spectroscopy
3. Mass Spectrometry
4. 1H-NMR Spectroscopy
5. 13C-NMR Spectroscopy
V. Artifacts
VI. Separation Methods
VII. Physical and Spectroscopic Properties of Anthraquinones (Table 7)
VIII. Rubiaceae Species Containing Anthraquinones (Table 8)
- References
- Recent Developments in the Field of Marine Natural Products with Emphasis on Biologically Active Compounds
I. Introduction
II. Porifera
11.1. Steroids from Porifera
11.2. Terpenoid Constituents from Porifera
11.3. Amino Acid Derived Metabolites from Porifera
11.4. Peptide Alkaloids, Peptides, and Proteins from Porifera
11.5. Nucleosides from Porifera
11.6. Alkaloids and Other Heterocyclic Compounds from Porifera
11.7. Macrolides from Porifera
11.8. Phenols and Aromatic Ethers from Porifera
11.9. Carboxylic Acids