Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products
Springer Wien (Verlag)
978-3-7091-8989-4 (ISBN)
Chemical Ecology and the Social Behavior of Animals.- 1. Introduction.- 2. Terminology.- 3. Origin.- 4. Pheromones as a Multicomponent System.- 5. Perception of Pheromones by Insects and Vertebrates.- 6. Chemical Communication in Vertebrates.- 7. Endocrine Hormone-Pheromone Interaction.- 7.1 Bruce Effect.- 7.2 Whitten Effect.- 7.3 Lee-Boot Effect.- 7.4 Ropartz-Effect.- 8. Maternal Pheromones.- 9. Chemical Communication in Marine Organisms.- 10. The Effect of Anosmia.- 11. Chemical Communication in Invertebrates.- 12. Caste and Kin Recognition in Social Insects.- 13. Insect Sex Pheromones.- 14. Role of Pheromones in Reproductive Isolation of Insects.- 15. Arthropod Defensive Secretions.- 16. Defense in Termites.- 17. Predator-Prey Interactions.- 18. Human Pheromones.- 19. Conclusion.- Acknowledgements.- References.- Phenolic Compounds of the Mulberry Tree and Related Plants.- I. Introduction.- II. Flavonoids Carrying Isoprenoid Substituents Isolated from the Japanese Cultivated Mulberry Tree.- 1. Isolation of Flavonoids Carrying Isoprenoid Substituents.- 2. Structures of Flavonoids Carrying Isoprenoid Substituents.- 3. Synthesis of Tetrahydrokuwanon C Tetramethyl Ether.- III. Photo-Oxidative Cyclization of Prenylflavones.- 1. Photo-Oxidative Cyclization of Morusin.- 2. Mechanism of the Photo-Oxidative Cyclization of Morusin.- 3. Oxidative Cyclization of Morusin.- IV. Phytoalexins and Antifungal Substances in the Mulberry Tree.- V. Diels-Alder Type Adducts of the Cultivated Mulberry Tree.- 1. Hypotensive Constituents, Kuwanons G and H.- 2. Five Novel 2-Arylbenzofuran Derivatives, Chalcomoracin, Mulberrofurans C, F, G, and H.- 3. Coloring Matter of Morus Root Bark, Mulberrofuran I.- 4. Other Phenolic Compounds Related to Mulberrofuran I.- 5. Diels-Alder Type Adducts of Morus Cell Cultures.- 6. Other Diels-Alder Type Adducts of Cultivated Mulberry Tree.- VI. Phenolic Constituents of the Crude Drug "Sang-Bai-Pi".- 1. Structures of the Flavonoids Carrying Isoprenoid Substituents Isolated from "Sang-Bai-Pi".- 2. Structures of Diels-Alder Type Adducts of "Sang-Bai-Pi".- VII. Absolute Configuration of Diels-Alder Type Adducts from Morus Sp..- 1. Classification of Diels-Alder Type Adducts.- 2. Stereochemistry of Diels-Alder Type Adducts.- 3. Absolute Configuration of Mulberrofurans C and J by CD Spectra.- 4. Absolute Configuration of Other Diels-Alder Type Adducts.- 5. Absolute Configuration of the Chiral Centers on the Cyclohexene Ring of Kuwanon L.- 6. Absolute Configuration of the Ketal Compounds, Mulberrofurans F, G, and K.- VIII. Phenolic Constituents of Cudrania tricuspidata (Carr.) Bur. and Broussonetia Sp..- 1. Structures of Xanthone and Flavonoid Derivatives from Cudrania tricuspidata (Carr.) Bur..- 2. Structures of 1,3-Diphenylpropane and Flavonoid Derivatives from Broussonetia Sp.- IX. Biological Activities of Phenolic Constituents of Mulberry Tree and Related Plants.- Acknowledgements.- References.- N-Hydroxyamino Acids and Their Derivatives.- I. Introduction, Scope and Nomenclature.- II. N-Hydroxyamino Acid Residues as Fragments of Natural Products.- III. Physical and Chemical Properties.- IV. Analysis.- V. Naturally-Occurring N-Hydroxypeptides.- VI. Biological Action of N-Hydroxyamino Acids and N-Hydroxypeptides.- VII. Biogenesis of the N-Hydroxyamide Bond.- VIII. Synthesis of N-Hydroxyamino Acids and Their Derivatives.- 1. Reaction of Nitric Oxide with 1,3-Diketo Derivatives.- 2. Strecker Synthesis.- 3. Reduction of Nitro Acids and Nitro Esters.- 4. Reduction of Oximes of ?-Keto Acids and Substituted Aldoximes.- 5. Addition of Hydroxylamine to ?,?-Unsaturated Acids.- 6. Reaction of ?-Halo Acids with Hydroxylamine.- 7. Reaction of ?-Halo Acids with Benzyloxyamine.- 8. From N-Tosyl-O-Benzylhydroxylamine.- 9. From Nitrones.- 9.1. Substitution.- 9.2. Addition.- 10. From Oxaziridines.- 11. Alkylation of Hydroxamic Acids.- 12. Synthesis of N-Hydroxy-sec-amino Acids.- 13. Esterification of N-Hydroxyamino Acids and N-Alkoxyam
Erscheint lt. Verlag | 9.1.2012 |
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Reihe/Serie | Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products |
Co-Autor | L.F. Alves, A. Chimiak, M.J. Milewska, T. Nomura |
Zusatzinfo | VIII, 311 p. |
Verlagsort | Vienna |
Sprache | englisch |
Maße | 152 x 229 mm |
Gewicht | 470 g |
Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Pharmakologie / Pharmakotherapie |
Medizin / Pharmazie ► Pharmazie | |
Naturwissenschaften ► Biologie ► Biochemie | |
Naturwissenschaften ► Chemie ► Organische Chemie | |
Schlagworte | Amino acid • biochemistry • Chemistry • natural product • Polymer |
ISBN-10 | 3-7091-8989-6 / 3709189896 |
ISBN-13 | 978-3-7091-8989-4 / 9783709189894 |
Zustand | Neuware |
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