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  • 1
    UID:
    almahu_9949983226402882
    Format: 1 online resource (530 p.)
    Edition: First edition.
    ISBN: 9780128034439 , 0128034432
    Series Statement: The Alkaloids, Volume 75
    Note: Description based upon print version of record. , Front Cover; The Alkaloids Chemistry and Biology; Copyright; Contents; CONTRIBUTORS; PREFACE; One - Simple Indolizidine and Quinolizidine Alkaloids; 1. INTRODUCTION; 2. INDOLIZIDINE ALKALOIDS FROM FUNGAL AND MICROBIAL SOURCES; 2.1 Slaframine; 2.2 Cyclizidine and JBIR-102; 2.3 Streptomyces Metabolites; 2.4 Pantocins A and A2; 3. HYDROXYLATED INDOLIZIDINE ALKALOIDS; 3.1 General Reviews; 3.2 1-Hydroxyindolizidines; 3.3 Lentiginosine and Related Compounds; 3.3.1 Isolation and Biological Activity; 3.3.2 Synthesis; 3.3.2.1 Routes Employing Late-Stage C-1/C-2 Bond Formation , 3.3.2.2 Routes Employing Late-Stage Alkylative C-3/N Bond Formation3.3.2.3 Routes Employing Late-Stage Acylative C-3/N Bond Formation; 3.3.2.4 Routes Employing Late-Stage N/C-5 Bond Formation; 3.3.2.5 Routes Employing Double Cyclization with C-3/N/C-5 Bond Formation; 3.3.2.6 Simultaneous Formation of N/C-5 and C-8/C-8a Bonds: An Aza-Diels-Alder Approach; 3.3.2.7 Routes Employing Late-Stage C-6/C-7 or C-7/C-8 Bond Formation; 3.3.2.8 Routes Employing Late-Stage C-8/C-8a Bond Formation; 3.4 Steviamine; 3.5 Swainsonine; 3.5.1 Occurrence, Isolation, and Characterization; 3.5.2 Synthesis , 3.5.2.1 Routes Employing Late-Stage C-1/C-2 Bond Formation3.5.2.2 Routes Employing Late-Stage C-3/N Bond Formation; 3.5.2.3 Routes Employing Late-Stage N/C-5 Bond Formation; 3.5.2.4 Routes Employing Tandem Cyclizations with C-3/N/C-5 or N/C-5/C-8a Bond Formation; 3.5.2.5 Routes Employing Late-Stage C-6/C-7 Bond Formation; 3.5.2.6 Routes Employing Late-Stage Bond Formation to C-8a; 3.5.3 Biological Activity; 3.5.3.1 Glycosidase Inhibition; 3.5.3.2 Swainsonine Toxicosis and Lysosomal Storage Diseases; 3.5.3.3 Anticancer and Immunomodulatory Effects; 3.6 Castanospermine and Related Compounds , 3.6.1 Isolation and Structure3.6.2 Synthesis; 3.6.2.1 Routes Employing Late-Stage C-3/N Bond Formation; 3.6.3.2 Routes Employing Late-Stage N/C-5 Bond Formation; 3.6.2.3 Routes Employing Late-Stage C-6/C-7 Bond Formation; 3.6.2.4 Routes Employing Late-Stage Bond Formation to C-8a; 3.6.3 Biological Activity; 3.6.3.1 Glycosidase Inhibition; 3.6.3.2 Antiviral Activity; 3.6.3.3 Other Biological Effects; 3.7 The Putative Uniflorines; 4. PLANT INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDS BEARING ALKYL, FUNCTIONALIZED ALKYL, OR ALKENYL SUBSTITUENTS; 4.1 Dendroprimine; 4.2 Prosopis Alkaloids , 4.3 5,6,7,8-Tetrahydroindolizine Alkaloids4.4 Anibamine; 4.5 Elaeocarpus Alkaloids; 4.5.1 Isolation and Characterization; 4.5.2 Biogenesis; 4.5.3 Synthesis; 4.6 Lupin Alkaloids; 4.6.1 Occurrence and Characterization; 4.6.2 Structural Investigations; 4.6.3 Synthesis; 4.6.3.1 Syntheses of Tashiromine; 4.6.3.2 Syntheses of Lupinine and Epilupinine; 4.6.3.3 Synthesis of (+)-Hupeol; 4.7 Myrtine and Epimyrtine; 4.8 Lycopodium Alkaloids; 4.8.1 Isolation and Characterization; 4.8.2 Synthesis; 4.9 Porantheridine; 4.10 Plumerinine , 5. PLANT INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDS BEARING ARYL OR HETEROARYL SUBSTITUENTS , English
    Additional Edition: ISBN 9780128034347
    Additional Edition: ISBN 0128034343
    Language: English
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