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 16
Contribuţii de J. Bonner, K. Freudenberg, H. Kuhn, E.E. Van Tamelen, Z. Valenta, K. Weinges, K. Wiesneren Limba Engleză Paperback – 22 ian 2012
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Specificații
ISBN-13: 9783709180495
ISBN-10: 370918049X
Pagini: 240
Ilustrații: VI, 228 p.
Dimensiuni: 155 x 235 x 13 mm
Greutate: 0.34 kg
Ediția:Softcover reprint of the original 1st ed. 1958
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: 370918049X
Pagini: 240
Ilustrații: VI, 228 p.
Dimensiuni: 155 x 235 x 13 mm
Greutate: 0.34 kg
Ediția:Softcover reprint of the original 1st ed. 1958
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
— Table des matières.- Catechine, andere Hydroxy-flavane und Hydroxy-flavene.- 1. Ältere Arbeiten.- 2. Die bekannten Hydroxy-flavane.- 3. Eigenschaften, Herstellung der Hydroxy-flavane.- 4. Kondensation durch Säuren.- 5. Hydroxy-flavene.- 6. Leucoanthocyanidin-hydrate, Acetate der Pseudoanthocyanidine und der Pseu doanthocyanidin-hydride.- 7. Oxydations- und Reduktionsübergänge in der C6C3C6-Reihe.- 8. Cyanomaclurin.- 9. Catechin-3-gallat und Catechin-3-glucosid.- 10. Stereochemie der Catechine.- 11. Biogenese der C6C3C6-Gruppe.- Recent Progress in the Chemistry of the Aconite-Garrya Alkaloids 26.- I. Introduction.- II. Garry a Alkaloids.- 1. The Structure of Veatchine and Garryine.- Environment of the Nitrogen.- Structure of the Skeleton.- Structure of the Oxoveatchine Dicarboxylic Acids.- Structure Assignment to Veatchine and Garryine.- 2. The Stereochemistry of the Garrya Skeleton and its Influence on the Properties of Garrya Alkaloids.- 3. The Structure of Cuauchichicine and Garryfoline.- 4. Configuration of the Secondary Hydroxyl Group in Veatchine and Garryfoline.- III. The Structure of Atisine.- Original Degradation Work on Atisine.- Similarity of Atisine with the Garrya Alkaloids and the Deduction of the Atisine Structure.- Some Confirmatory Evidence.- IV. Biogenesis of Veatchine and Atisine and Consideration of the Stereochemistry of Atisine.- V. The Structure of Ajaconine.- VI. The Structure of Napelline.- VII. The Chemistry of Hetisine.- VIII. Lycoctonine and Delpheline.- 1. The Chemistry of Lycoctonine.- Oxidation Studies.- Skeletal Changes.- 2. The Chemistry of Delpheline.- Environment of the Nitrogen.- Transformations in the Demethylene Series.- The Carbon Skeleton of Delpheline.- 3. Biogenesis of Lycoctonine and Delpheline.- IX. The Chemistry ofDelphinine.- References.- Structural Chemistry of Actinomycetes Antibiotics.- 1. Actidione (Cycloheximide).- 2. Actinomycins.- 3. Actithiazic Acid.- 4. Amicetin.- 5. Aureomycin (Chlorotetracycline).- 6. Aureothricin and Thiolutin.- 7. Azaserine.- 8. Chloromycetin (Chloramphenicol).- 9. Cycloserine (Oxamycin).- 10. Elaiomycin.- 11. Erythromycin.- 12. Etamycin (Viridogrisein).- 13. Magnamycin (Carbomycin).- 14. Methymycin.- 15. Mycomycin.- 16. Netropsin.- 17. Nocardamine.- 18. Novobiocin.- 19. Puromycin (Achromycin).- 20. Sarkomycin.- 21. Streptomycin.- 22. Terramycin.- 23. Tetracycline.- 24. Valinomycin.- References.- Protein Synthesis in Plants.- I. Introduction.- II. Isolation of Microsomes.- III. Structure of the Microsomes.- IV. Role of the Microsomes in Protein Synthesis.- V. Biology of the Microsomes.- 1. Nuclear Microsomes.- 2. Origin of Microsomes.- 3. Transfer of Microsomal RNA.- 4. Synthesis of the Microsomal Components.- 5. Kinetics of Microsomal Labeling.- VI. Protein Synthesis as a Catenary Sequence.- 1. Amino Acid Activation.- 2. Transfer to Soluble RNA.- 3. The Microsome as Acceptor of Amino Acid.- 4. Alternative Pathways of Peptide Synthesis.- VII. Protein Synthesis in Mitochondria and Chloroplasts.- VIII. Protein Synthesis in Varied Plant Organs.- 1. Developing Fruits and Seeds.- 2. Leaves.- IX. Conclusion.- References.- The Electron Gas Theory of the Color of Natural and Artificial Dyes: Problems and Principles.- I. Some Experimental Facts Concerning Color and Structure.- 1. Poly acetylenes, Polyenes, Symmetrical Cyanine Dyes, and Some Similar Compounds.- 2. Aza Derivatives of Symmetrical Cyanine Type Compounds.- 3. Acridine Type Bridge Formation in Symmetrical Cyanine Type Compounds.- 4. Some Other Types of Resonance Systems Causing Absorption of Visible Light.- II. Some General Principles and Postulates.- 1. Light Quanta and the Einstein-Bohr Frequency Relation.- 2. Wave Particle Duality of the Electron and the de Broglie Relationship.- 3. Standing Electron Waves. The Pauli Principle.- 4. The Chemical Bond; a and n Electron States.- III. Quantum Mechanical Determination of the Position of the Absorption Bands of Simple Dyes.- 1. A Simple Model of Symmetrical Cyanine Dyes.- 2. A Simple Treatment of the Aza Derivatives of Symmetrical Cyanine Type Compounds.- References.- Namenverzeichnis. Index of Names. Index des Auteurs.- Sachverzeichnis. Index of Subjects. Index des Matières.