Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products / Progrès dans la Chimie des Substances Organiques Naturelles: Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products, cartea 20
Autor L. Zechmeisteren Limba Engleză Paperback – 18 oct 2011
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Specificații
ISBN-13: 9783709171554
ISBN-10: 3709171555
Pagini: 532
Ilustrații: XIV, 512 p.
Dimensiuni: 155 x 235 x 28 mm
Greutate: 0.74 kg
Ediția:Softcover reprint of the original 1st ed. 1962
Editura: SPRINGER VIENNA
Colecția Springer
Seria Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products
Locul publicării:Vienna, Austria
ISBN-10: 3709171555
Pagini: 532
Ilustrații: XIV, 512 p.
Dimensiuni: 155 x 235 x 28 mm
Greutate: 0.74 kg
Ediția:Softcover reprint of the original 1st ed. 1962
Editura: SPRINGER VIENNA
Colecția Springer
Seria Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products
Locul publicării:Vienna, Austria
Public țintă
ResearchCuprins
Nitrogen-containing Metabolites of Fungi.- I. Introduction.- II. Compounds Containing Acyclic Nitrogen.- III. Oligopeptides.- IV. Heterocyclic Nitrogen Compounds.- V. Heterocyclic Compounds Containing Sulphur as well as Nitrogen.- VI. Concluding Remarks.- References.- Forschungen am Lignin.- I. Einleitung.- II. Ligninpräparate.- III. Die Abbausäuren.- IV. Die destruktive Hydrierung des Lignins.- V. Weitere Eigenschaften des Lignins.- VI. Die p-Hydroxy-zimtalkohole.- VII. Die Herstellung des Dehydrierungspolymerisates (DHP).- VIII. Vergleich des natürlichen und des künstlichen Lignins.- IX. Zwischenprodukte der Ligninbildung.- X. Zur Biochemie und über Versuche mit Isotopen.- XI. Die Wachstumsprinzipien des Lignins.- XII. Die Bindung des Lignins an die Kohlenhydrate.- XIII. Bemerkungen zu den Entwürfen eines Konstitutionsschemas des Coniferenlignins.- XIV. Laubholzlignin. Humus.- Die Ubichinone (Coenzyme Q).- I. Einleitung.- II. Isolierung und Vorkommen der Ubichinone.- III. Physikalisch-chemische Eigenschaften der Ubichinone.- IV. Ermittlung der Konstitution der Ubichinone durch chemischen Abbau.- V. Synthesen der Ubichinone.- VI. Umwandlungsprodukte der Ubichinone.- VII. Biosynthese der Ubichinone.- VIII. Plastochinon (Koflers Chinon, Coenzym Q254).- IX. Biochemische Bedeutung der Ubichinone.- Bedeutung der Lipide für Electron-Transport-Systeme.- Naturally Occurring Aromatic Derivatives of Monocyclic ?-Pyrones.- I. Introduction and Historical Development.- II. Structural Elucidation.- III. Syntheses.- IV. Physical Properties.- V. Pharmacological Properties.- VI. Taxonomic Significance of the Distribution of ?-Pyrones in Lauraceae.- VII. Reflections on Biosynthesis and Phylogenesis.- Addendum.- References.- Anthocyanins and their Sugar Components.- I.Introduction.- II. Isolation.- III. Properties of Anthocyanins.- IV. Identification of Anthocyanins.- V. Natural Occurrence.- VI. Distribution of Anthocyanins.- VII. Anthocyanins and Plant Colour.- VIII. Biosynthesis of Anthocyanins.- IX. Conclusion.- References.- Aminozucker, Synthesen und Vorkommen in Naturstoffen.- Verzeichnis der Abkürzungen.- I. Einleitung. Nomenklatur.- II. Allgemeine Reaktionen von Aminozuckern.- III. Synthesen von Aminozuckern.- IV. Aminozucker-haltige Naturstoffe.- V. Enzymatischer Aufbau und Abbau von Aminozuckern.- Structure and Stereochemistry of the Lycopodium Alkaloids.- I. Introduction.- II. The Structure of Annotinine.- III. The Structure of Lycopodine.- IV. The Structures of Some Related Alkaloids.- V. Stereochemistry and Interrelations of Alkaloids with the Lycopodine Skeleton.- VI. The Pyridone and Pyridine Alkaloids of Lycopodium.- VII. The Biogenesis of the Lycopodium Alkaloids.- References.- Newer Developments in the Field of Veratrum Alkaloids.- I. Introduction.- A. The Jerveratrum Alkaloids.- II. Rubijervine and Isorubijervine.- III. Jervine and Veratramine.- IV. On the Configuration of Jervine and Veratramine.- V. Glycosides of the Alkamines.- VI Alkaloids of Unknown Structure.- VII. Pharmacological Activity.- B. The Ceveratrum Alkaloids.- VIII. Occurrence.- IX. Cevine.- X. Germine.- XI. Zygadenine.- XII. Protoverine.- XIII. Some General Remarks.- XIV. Alkaloids of Unknown Structure.- XV. Pharmacological Activity of Veratrum Alkaloids.- XVI. Synthetic Esters and their Pharmacological Effects.- XVII. Biogenesis of Veratrum Alkaloids.- References.- Equilibrium Sedimentation of Macromolecules and Viruses in a Density Gradient.- I. Introduction.- II. Experimental Procedures.- III. Theoretical Considerations and Evaluation ofResults.- IV. Applications to Some Physical and Biological Problems.- V. Tables.- References.- Current Theories on the Origin of Life.- I. Introduction.- II. The Nature of Living Organisms.- III. The Origin of Life on the Earth.- IV. Space Research and the Origin of Life.- References.- Namenverzeichnis. Index of Names. Index des Auteurs.- Sachverzeichnis. Index of Subjects. Index des Matières.