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Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products
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Main description:

The volumes of this classic series, now referred to simply as Zechmeister after its founder, L. Zechmeister, have appeared under the Springer Imprint ever since the series' inauguration in 1938. The volumes contain contributions in various topics related to the origin, distribution, chemistry, synthesis, biochemistry, function or use of various classes of naturally occurring substances ranging from small molecules to biopolymers. Each contribution is written by a recognized authority in his field and provides a comprehensive and up-to-date review of the topic in question. Addressed to biologists, technologists, and chemists alike, the series can be used by the expert as a source of information and literature citations and by the non-expert as a means of orientation in a rapidly developing discipline.


Contents:

Amino Acids from Mushrooms..- I. Introduction.- II. General Methods.- III. Structure, Occurrence and Biochemistry.- 1. Neutral Aliphatic Amino Acids.- 1.1. Hydroxyvaline, Hydroxyleucines, and Hydroxyisoleucines.- 1.1.1. 3-Hydroxyvaline.- 1.1.2. 4-Hydroxyleucine.- 1.1.3. 4,5-Dihydroxyleucine.- 1.1.4. 4,5,5?-Trihydroxyleucine.- 1.1.5. 4-Hydroxyisoleucine.- 1.1.6. 4,5-Dihydroxyisoleucine.- 1.2. Other Hydroxyamino Acids.- 1.2.1. 2-Amino-3,4-dihydroxybutanoic Acid.- 1.2.2. 2-Amino-4-ethoxy-3-hydroxybutanoic Acid.- 1.2.3. 4-Hydroxynorvaline.- 1.2.4. 2-Amino-7-hydroxyoctanoic Acid.- 1.3. Unsaturated Leucine and Isoleucine Homologues.- 1.3.1. 2-Amino-5-methyl-4-hexenoic Acid.- 1.3.2. 2-Amino-4-methyl-5-hexenoic Acid.- 1.3.3. 3-Methylenenorvaline.- 1.3.4. 2-Amino-3-hydroxymethyl-3-pentenoic Acid and 2-Amino-3-formyl-3-pentenoic Acid.- 1.3.5. 2-Amino-3-methylenehexanoic Acid.- 1.4. Unsaturated Norvalines and Norleucines, and Related Amino Acids.- 1.4.1. 2-Amino-3-butenoic Acid.- 1.4.2. Allylglycine and Propargylglycine.- 1.4.3. 2-Amino-3-hydroxy-4-pentynoic Acid.- 1.4.4. 2-Amino-5-hexenoic Acid.- 1.4.5. 2-Amino-4-hexynoic Acid.- 1.4.6. 2-Amino-5-hexynoic Acid.- 1.4.7. 2-Amino-3-hydroxy-4-hexynoic Acid.- 1.4.8. 2-Amino-6-hydroxy-4-hexynoic Acid.- 1.4.9. 2-Amino-4,5-hexadienoic Acid.- 1.4.10. 2-Aminohept-4-en-6-ynoic Acid.- 1.4.11. Cyclopropylalanine.- 1.5. Unsaturated Chloroamino Acids.- 1.5.1. 2-Amino-4-chloro-4-pentenoic Acid.- 1.5.2. Chlorocrotylglycine.- 1.5.3. 2-Amino-5-chloro-6-hydroxy-4-hexenoic Acid.- 1.5.4. 2-Amino-5-chloro-5-hexenoic Acid.- 1.5.5. 2-Amino-5-chloro-4-hydroxy-5-hexenoic Acid.- 2. Acidic Amino Acids.- 2.1. Hydroxyaspartic Acid.- 2.2. 4-Substituted Glutamic Acids.- 2.2.1. 4-Methylene-, 4-Ethylidene-, and 4-Propylideneglutamic Acid.- 2.2.2. 4-Methylglutamic Acid.- 2.3. 2-Amino-4-methylpimelic Acid.- 2.4. 3-Nitraminoalanine and 2-Amino-4-nitraminobutanoic Acid.- 3. Heterocyclic Amino Acids.- 3.1. Azetidine-2-carboxylic Acid and Derivatives.- 3.1.1. Azetidine-2-carboxylic Acid.- 3.2. Derivatives of Proline.- 3.2.1. 3-Aminoproline.- 3.3. Pipecolic Acid and Derivatives.- 3.3.1. 5-Hydroxypipecolic Acid.- 3.3.2. 3-Hydroxybaikiain.- 4. Amino Acids Containing Heterocycles.- 4.1. Pyrrolidine Amino Acids.- 4.1.1. 1-(3-Amino-3-carboxypropyl)-5-oxo-2-pyrrolidinecarboxylic Acid.- 4.2. Isoxazoline Amino Acids.- 4.2.1. Tricholomic Acid.- 4.2.2. Ibotenic Acid and Muscimol.- 4.2.3. Muscazone.- 4.3. Amino Acids Derived from Phenylalanine.- 4.3.1. Stizolobic Acid and Stizolobinic Acid.- 4.3.2. Muscaflavin.- 4.3.3. Betalains.- 4.3.4. Acromelic Acid A and Acromelic Acid B.- 4.4. Oxygen Heterocyclic Amino Acids.- 4.4.1. 3-(3-Carboxyfuran-4-yl)alanine.- 4.4.2. Lycoperdic Acid.- 5. Aromatic Amino Acids.- 5.1. Derivatives of Phenylalanine.- 5.1.1. 3,4-Dihydroxyphenylalanine.- 5.1.2. 4-Hydroxy-3-methoxyphenylalanine.- 5.2. Derivatives of Tryptophan.- 6. Miscellaneous Amino Acids.- 7. ?-Glutamyl Compounds.- 7.1. ?-Glutamyl Compounds of Protein Amino Acids.- 7.1.1. ?-Glutamylglycine.- 7.1.2. ?-Glutamylmethionine.- 7.1.3. ?-Glutamylcystine and Related Compounds.- 7.1.4. ?-Glutamylglutamic Acid.- 7.1.5. ?-Glutamylhistidine and ?-Glutamyllysine.- 7.2. ?-Glutamyl Compounds of Non-Protein Amino Acids.- 7.2.1. ?-Glutamyl-?-alanine.- 7.2.2. ?-Glutamyl-2-amino-4-hexynoic Acid and ?-Glutamyl-2-amino-3-hydroxy-4-hexynoic Acid.- 7.2.3. ?-Glutamyl-?-ornithine.- 7.2.4. ?-Glutamyl-3-aminoproline.- 7.2.5. ?-Glutamylnicotianine.- 7.3. ?-Glutamylpeptides of Amines.- 7.3.1. N-(?-Glutamyl)ethanolamine.- 7.3.2. Theanine.- 7.3.3. ?-Glutamyl-2-amino-3-hexanone.- 7.3.4. ?-Glutamyl-N-nitroethylenediamine.- 7.3.5. Coprine.- 7.4. Agaritine and Related Compounds.- 7.4.1. ?-Glutaminyl-4-hydroxybenzene.- 7.4.2. Agaritine.- 7.4.3. Xanthodermine.- 7.4.4. Agaridoxin.- 7.5. ?-Glutamyl Compounds Producing Odoriferous Substances.- 7.5.1. Lentinic Acid.- 7.5.2. ?-Glutamylmarasmine.- IV. Conclusions.- Acknowledgments.- Mushroom Index.- References.- Cembranoids, Pseudopteranoids, and Cubitanoids of Natural Occurrence..- I. Introduction.- A. Structural Representation and Nomenclature.- II. Cembranoids from Plants.- A. Plants Other than Tobacco.- B. Tobacco.- 1. Oxidation of the 11,12 Double Bond.- 2. Oxidation of the 7,8 Double Bond.- 3. Oxidation at Positions Allylic to the 11,12 Double Bond.- 4. Oxidation of the Hydroxy Group at C-6.- 5. Acid-Induced Reactions.- III. Cembrenes from Insects.- IV. Cembranoids from Marine Invertebrates.- A. Gorgonacea.- 1. Eunicea Species.- 2. Lophogorgia and Leptogorgia Species.- 3. Plexaura Species.- 4. Pseudopterogorgia Species.- B. Alcyonacea.- 1. Alcyonium Species.- 2. Gersemia Species.- 3. Lobophytum Species.- 4. Sarcophyton Species.- 5. Sinularia Species.- C. Stolonifera.- V. Pseudopteranoids from Marine Invertebrates.- Addendum-Cubitanoids.- Acknowledgements.- References.- Author Index.


PRODUCT DETAILS

ISBN-13: 9783709191521
Publisher: Springer (Springer Verlag GmbH)
Publication date: February, 2012
Pages: 328
Weight: 528g
Availability: Available
Subcategories: Biochemistry, Pharmacology
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