Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products: Fortschritte der Chemie organischer Naturstoffe Progress in the Chemistry of Organic Natural Products, cartea 41
Contribuţii de J.W. Daly, D. Ferreira, S J Gould, E. Haslam, D.J. Robins, D.G. Roux, S.M. Weinreben Limba Engleză Paperback – 12 feb 2012
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Specificații
ISBN-13: 9783709186589
ISBN-10: 3709186587
Pagini: 384
Ilustrații: VIII, 376 p.
Dimensiuni: 155 x 235 x 20 mm
Greutate: 0.54 kg
Ediția:Softcover reprint of the original 1st ed. 1982
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: 3709186587
Pagini: 384
Ilustrații: VIII, 376 p.
Dimensiuni: 155 x 235 x 20 mm
Greutate: 0.54 kg
Ediția:Softcover reprint of the original 1st ed. 1982
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
The Metabolism of Gallic Acid and Hexahydroxydiphenic Acid in Higher Plants..- 1. Polyphenol Biosynthesis in Higher Plants — An Overview.- 2. Metabolites of Gallic Acid.- 3. The Ellagitannins.- 4. Postscript.- References.- The Direct Biomimetic Synthesis, Structure and Absolute Configuration of Angular and Linear Condensed Tannins..- I. Introduction.- II. Bonding Positions at Nucleophilic Centres.- III. Conditions for Interflavanoid Bonding. Stereochemical Course of the Reaction. Chiroptical Method for Determining the Absolute Configuration at C-4.- IV. Direct Biomimetic Synthesis of Biflavanoids.- V. Direct Biomimetic Synthesis of “Angular” Triflavanoids.- VI. Biflavanoids and a “Linear” Triflavanoid with Terminal 3,4-Diol Function.- VII. Composition of the Metabolic Pool and Condensation Aptitudes of Tannin Precursors.- References.- Streptonigrin.- I. Introduction.- II. Isolation and Structure.- III. Structure Activity Relationships and Mechanism of Action.- IV. Biosynthesis.- V. Synthetic Studies.- References.- The Pyrrolizidine Alkaloids.- I. Introduction.- II. The Necine Bases.- III. The Necic Acids.- IV. The Pyrrolizidine Alkaloids.- V. Pyrrolizidine Derivatives in the Lepidoptera.- VI. Biosynthesis.- VII. Pharmacology.- VIII. Table 1. List of Plant Genera Containing Pyrrolidine Alkaloids.- Table 2. Alkaloid Content of Plant Species Which Have Been Investigated.- Table 3. The Structures of the Pyrrolizidine Alkaloids.- References.- Addendum.- Alkaloids of Neotropical Poison Frogs (Dendrobatidae).- I. Introduction.- II. Batrachotoxins.- III. Pumiliotoxin-C Class (cis-decahydroquinolines).- IV. Histrionicotoxins.- V. Gephyrotoxins.- VI. Pumiliotoxin-A Class.- VII. Other Alkaloids.- A. Structures, Properties, and Occurrence.- References.- Author Index.