Studies in Natural Products Chemistry: Structure and Chemistry (Part F)
Natural Products Chemistry continues to grow at an increasing pace and this growth is reflected in the present volume of Studies in Natural Products Chemistry, which is the 20th of this series. The first 20 volumes were largely devoted to structure and synthesis of various classes of natural products, irrespective of their bioactivity. Subsequent volumes of this series will however be devoted to the chemistry of bioactive natural products and will therefore a departure from the earlier volumes.
The present volume contains contributions from a number of eminent scientists and covers interesting reviews on terpenes, alkaloids and other types of natural products reported from terrestrial and marine sources. Comprehensive indexes covering all the 20 volumes have been prepared which include a Cumulative General Subject Index along with more focused Cumulative Indices on Organic Synthesis, Pharmacological Activity and Biological Source. This comprehensive indexing of the volumes should make the entire series much more valuable and user-friendly.
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Chapter 6 Natural Products by Oxidative Phenolic Coupling Phytochemistry Biosynthesis and Synthesis
Chapter 7 Narcissus Alkaloids
Chapter 8 Total Synthesis of Naphthylisoquinoline Alkaloids
Chapter 11 Synthesis of Carotenoids
Chapter 12 Structure Elucidation of Phenylpropanoid Wood Extractives
Chapter 13 Chemical and Biological Investigations of Salvia Species Growing in Turkey
Chapter 14 The Chemistry of Some Natural Colourants
Chapter 15 Bioactive Natural and Synthetic Acronycine Derivatives Modified at the Pyran Ring
Chapter 16 Chiral Synthons by Selective Redox Reactions Catalysed by Hitherto Unknown Enzymes Present in Resting Microbial Cells
Chapter 17 Microcystins and Nodularins Hepatotoxic Cyclic Peptides of Cyanobacterial Origin
Chapter 9 DNA Damaging Natural Products with Potential Anticancer Activity
Chapter 10 In Vitro Models of Human Disease States
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Abstr acetate acetyl acid acronycine Acta activity agents alcohol aldehyde alkaloids allylic antimalarial antitumor aromatic Artemisia aryl assay asymmetric atropisomer baccata biaryl bioactive bioassay biosynthesis bond Cancer carbon carboxylates carotenoids cell lines Chem chemical Chemistry chiral chloride colourant compounds coupling crinitol cuspidata cytotoxic dehydrogenation derivatives doid drugs enoate reductase enzyme epoxide ester ether extracts Fdez formation glycosides H NMR H-NMR hydrogen hydrolysis hydroxyl incomparabilis Mill inhibition inhibitor intramolecular isolated isomers ketone lactone lignans mediators MeOH methyl microcystin molecular NADH natural products nodularin OMe OMe oxidation Pharm phenolic Physalin Phytochemistry plant presence Prod productivity number Products Chemistry protein protons pseudonarcissus pyridine racemic reagent rearrangement reduction ring Salvia Scheme side chain signals Sē Sē sodium somnifera species spectral stereochemistry stereoselective structure substrate Table tazetta Tetrahedron Lett thermoaceticum toxicity withanolides Wittig reaction yeast yield