A gossauer (25 risultati)

artefacts (1) (S. A. Plant Physiol. Biochem. 34, 1) 1996. S. 77 - 83. m. zahlr. Abb. geklammert -2) Sonderabdruck.

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Paperback. Condizione: Brand New. bilingual edition. 231 pages. German language. 9.25x6.10x0.54 inches. In Stock.

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Buch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Monopyrrolic Natural Compounds Including Tetramic Acid Derivatives.- 1. Introduction.- 2. Pyrroles from Vertebrates.- 3. Pyrroles from Invertebrates.- 4. Pyrroles from Plants.- 5. Pyrroles from Fungi.- 6. Pyrroles from Bacteria.- References.- Author Index.…

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Paperback. Condizione: Brand New. reprint edition. 456 pages. German language. 9.25x6.10x1.04 inches. In Stock.

Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Pyrrol-that construct which flaunts its chemical versatility through having achieved the distinction of being the dominant sub-unit in the characteristic coloring matters of both the animal and plant king doms-is a fascinating entity. The determined skeptic will be well ad vised to keep his distance from this book, for only the most obdurate could fail to be captivated by the enormous wealth of detail collected, correlated, and presented here in eminently readable form. It seems certain that this work will be the indispensable hand maiden of all who would essay to embellish the lovely garden of pyrrol chemistry for a generation, and I will hazard the surmise that it will stimulate many to join that group. Inevitably, the appearance of this volume invites comparison with the great monograph on pyrrol chemistry given to the chemical com munity forty years ago by Hans Fischer and Hans Orth. That invaluable earlier work had a unique character; one cannot resist the temptation to express the opinion that that character was Hans Fischer, whose love for pyrrol and the superb array of substances related to it was his life. The book which he and Orth produced was essentially a detailed ac count of the ways in which pyrrols can be made-a practical and highly useful description of the state of synthetic art in 1934 in the special field to which Fischer himself had made such enormous contributions.…

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Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Monopyrrolic Natural Compounds Including Tetramic Acid Derivatives (Albert Gossauer) Introduction / Pyrroles from Vertebrates / Pyrroles from Invertebrates / Pyrroles from Plants / Pyrroles from Fungi / Pyrroles from Bacteria / ReferencesMonopyrrolic Na. …

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Monopyrrolic Natural Compounds Including Tetramic Acid Derivatives (Albert Gossauer) Introduction / Pyrroles from Vertebrates / Pyrroles from Invertebrates / Pyrroles from Plants / Pyrroles from Fungi / Pyrroles from Bacteria / ReferencesMonopyrrolic Na. …

Buch. Condizione: Neu. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products 86 | A. Gossauer | Buch | Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products | vii | Englisch | 2003 | Springer | EAN 9783211838891 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu Print on Demand.…

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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Pyrrol-that construct which flaunts its chemical versatility through having achieved the distinction of being the dominant sub-unit in the characteristic coloring matters of both the animal and plant king doms-is a fascinating entity. The determined skeptic will be well ad vised to keep his distance from this book, for only the most obdurate could fail to be captivated by the enormous wealth of detail collected, correlated, and presented here in eminently readable form. It seems certain that this work will be the indispensable hand maiden of all who would essay to embellish the lovely garden of pyrrol chemistry for a generation, and I will hazard the surmise that it will stimulate many to join that group. Inevitably, the appearance of this volume invites comparison with the great monograph on pyrrol chemistry given to the chemical com munity forty years ago by Hans Fischer and Hans Orth. That invaluable earlier work had a unique character; one cannot resist the temptation to express the opinion that that character was Hans Fischer, whose love for pyrrol and the superb array of substances related to it was his life. The book which he and Orth produced was essentially a detailed ac count of the ways in which pyrrols can be made-a practical and highly useful description of the state of synthetic art in 1934 in the special field to which Fischer himself had made such enormous contributions. 460 pp. Deutsch.…

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. 1. Struktur des Pyrrol-Molekuels.- 1.1. Geschichtliche Einleitung.- 1.2. Bezifferung des Pyrrol-Ringes und Nomenklatur seiner Derivate.- 1.3. Makroskopische physikalische Konstanten.- 1.4. Die Geometrie des Pyrrol-Molekuels.- 1.5. Die Elektronen-Struktur des . …

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -1. Struktur des Pyrrol-Moleküls.- 1.1. Geschichtliche Einleitung.- 1.2. Bezifferung des Pyrrol-Ringes und Nomenklatur seiner Derivate.- 1.3. Makroskopische physikalische Konstanten.- 1.4. Die Geometrie des Pyrrol-Moleküls.- 1.5. Die Elektronen-Struktur des Pyrrol-Moleküls.- 1.6. Grundzustands-Eigenschaften.- 2. Analytische Methoden.- 2.1. Farbreaktionen.- 2.2. Chromatographische Analyse.- 2.3. Polarographische Analyse.- 2.4. Elektronenspektren.- 2.5. IR-Spektren.- 2.6. Kernresonanzspektren.- 2.7. Massenspektren.- 3. Reaktivität der Pyrrole.- 3.1. Elektrophile Substitution.- 3.2. Diels-Alder-Reaktion.- 3.3. Reaktionen mit Carbenen.- 3.4. Säure-Base-Eigenschaften.- 3.5. Radikal-Reaktionen.- 3.6. Umlagerungs-Reaktionen.- 3.7. Hydrierung von Pyrrolen.- 3.8. Oxydation.- 3.9. Photochemie.- 4. Fyrrol-Metall-Derivate.- 4.1. Alkalimetall-Salze und Magnesyl-Derivate der Pyrrole.- 4.2. -Komplexe der Übergangsmetalle.- 4.3. -Komplexe der Übergangsmetalle.- 4.4. Additions-Verbindungen.- 4.5. Metall-Chelate.- 4.6. Pyrrol-Clathrate.- 4.7. Pyrrol-Derivate mit Halb-und Nichtmetallen.- 5. Pyrrole als Naturprodukte.- 5.1. Pyrrol-Farbstoffe.- 5.2. Pyrrol-Antibiotika aus Mikroorganismen.- 5.3. Pyrrole aus höheren Pflanzen.- 5.4. Pyrrole aus dem menschlichen und tierischen Organismus.- 6. Pyrrol-Ringsynthesen.- 6.1. C2N-C2-Cyclisierung.- 6.2. CN-C3-Cycnsierung.- 6.3. N-C2-C2-Cyclisierung.- 6.4. CNC-C2-Cyclisierung.- 6.5. N-C4-Cyclisierung.- 6.6. C4N-Cyclisierung.- 6.7. Pyrrole aus heterocyclischen Edukten.- 7. Synthetische Methoden.- 7.1. Abbau ringständiger Substituenten.- 7.2. Alkyl-Pyrrole.- 7.3. Aryl-Pyrrole.- 7.4. Acyl-pyrrole.- 7.5. Pyrrol-aldehyde.- 7.6. Vinylpyrrole.- 7.7. Pyrrol-carbonsäuren.- 7.8. Pyrrol-carbonsäurenitrile.- 7.9. Nitropyrrole.- 7.10.Nitrosopyrrole.- 7.11. Halogenpyrrole.- 7.12. Aminopyrrole.- 7.13. Hydroxypyrrole.- 7.14. Schwefel-und selenhaltige Pyrrole.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 460 pp. Deutsch.…