Studiebog
    Total Synthesis of Bioactive Natural Products

    Total Synthesis of Bioactive Natural Products

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    Bog E-bog
    • Format
    • Bog, paperback
    • Engelsk

    Beskrivelse

    Total Synthesis of Bioactive Natural Products provides step-by-step guidelines for effectively synthesizing the most promising bioactive agents from a broad range of natural products. Beginning with a concise background that outlines the benefits and challenges faced in effective synthesis, the book goes on to provide individual outlines for approximately 100 of the most promising bioactive agents. Taking a logical, user-friendly approach, the systematic name, compound class, structure, natural source, pharmaceutical potential and synthetic routes for each structure are detailed, with clear illustrations throughout, making this book an essential and practical guide for anyone working with both synthesis and natural products.

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    Detaljer
    • SprogEngelsk
    • Sidetal350
    • Udgivelsesdato27-04-2019
    • ISBN139780081028223
    • Forlag Elsevier / The Lancet
    • FormatPaperback
    Størrelse og vægt
  • Vægt570 g
    • coffee cup img
    10 cm
    book img
    15,1 cm
    22,9 cm

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    Diels-Alder reaction Hypericum perforatum Citrus fruits Claisen rearrangement Heck reaction Friedel-Crafts reaction Grignard reaction Epoxidation Cytotoxicity Coupling reaction Cross Metathesis Antibiotic Antioxidant Cytotoxic Hyperforin Antibacterial Anticancer Antiproliferative Antiviral Alkaloid Bombyx mori Antidepressant Antimicrobial Lignan Extra virgin olive oil Dess-Martin oxidation Cholesterol lowering Anti-tumor Antitumor Immunomodulatory Glycolipid 10-Membered macrolide (±)-3-Hydroxy-ß-ionone 3-Oxazolylindole alkaloid (+)-3-Oxo-a-ionol 5-Lipoxygenase inhibitor 7-Desmethoxyfusarentin 6-Deoxypladienolide D (-)-6-O-Desmethylantofine Ageladine A Agelas nakamurai Allelopathic Activity (+)-Ainsliadimer A Ainsliaea macrocephala [4 + 2]-Hetero-Diels-Alder dimerization Ancistrocladus ealaensis Allelopathic (-)-Andrographolide Amphidinium species (+)-Amphidinolide T1 Anogeissus acuminata Anti- Alzheimer’s antidiabetic (-)-Aiphanol Antipathogenic Anticanerous Antidengue Anti-HIV Ancistrotanzanine B Antitumor necrosis factor antagonism Anticancerous Antileishmanial Antrodia Camphorata Amide-Wittig olefination Aeruginosins 298-A and B Antimalarial Antiplatelet aggregation Bayer-Villiger oxidation Appel protocol Anolignan A Antiinflammatory Antileishmanials Anti-TMV Bauhinia purpurea Antrocamphin A Beilschmiedia kunstleri B. odoratissimum Bi-linderone Aiphanes aculeata Asymmetric Diels-Alder reaction Atroviridin Alder-Rickerts reaction Bisnorsesquiterpene A. tanzaniensis Austroplenckia populnea Baeyer-Villiger oxidation Bulbophylol-B Benzenoid Ancistroealaine A Basillus sp. strain B-60 Andrographis paniculata Brown allylation Birch reduction (+)-Chaetocin Anolignan B (+)-BINOL Chaetomium minutum Biomimetic cyclization Biphenyl ether derivative Bisnortriterpenoid Chugaev elimination Claisen cyclization Arenamide A Bauhinoxepin J Bischler-Napieralski reaction Corey-Bakshi-Shibata reduction Corey-Seabach umpolung method Barbier Reaction Cross-enyne metathesis Bombykol Cynanchum species Darzens reaction Dauben-Michno oxidative rearrangement Brown crotylation Diels-Alder cycloaddition Bulbophyllum kwangtungense Crabtree’s catalyst Daedalea dickinsii Danheiser’s protocol Caminoside A Caminus sphaeroconia Epidithiodiketopiperazine (ETP) alkaloid ent-Labdane diterpenoid Eschenmoser’s salt Dihydroisocoumarins Chromene-derivative Ciliatamides A and B Cyclooxygenases inhibitory activity Daedalin A Dictamnus dasycarpus Dienamide Clusia rosea Friedlander condensation Gliocladium roseum Cope rearrangement Furukawa cyclopropanation (+)-Harziphilone Cyclohexadepsipeptide f]oxepin Cyclopentenedione Hibarimicinone Croton steenkampianus Cylindol A Hünig''s base (+)-Gliocladin B Dess-Martin periodinane Dess-Martin periodinane oxidation Dihydrodibenz[b Integric acid Diterpenoid D-Hpla Intramolecular Dieckmann condensation Horner-Wadsworth-Emmons reaction Heat-shock protein 90 (HSP90) inhibitor Heck coupling Johnson-Claisen rearrangement Horner-Wardsworth-Emmons olefination Ito-Saegusa oxidation Ley oxidation Kumada-Tamao-Corriu coupling (±)-Marinopyrrole A L. erythrocarpa (±)-Limonin Lindera lucida Etnangien Evans-Carreria method Jones oxidation Karalicin (-)-Kunstleramide Kirschleger’s reaction L-Argol L-Choi Ley-Griffith oxidation Lindera aggregata Lindlar’s condition Linderaspirone A Garcinia atroviridis Herpes Simplex Virus 1 (HSV1) inhibitor Hepatoprotective (±)-Paecilomycine A Indole acyloin Jineol QUINOLINE ALKALOID (±)-Steenkrotin A (+)-Sattazolin Horner-Wadsworth-Emmon reaction Hoveyda-Grubbs catalyst Hoveyda-Grubbs second-generation catalyst (-)-Stagonolide A Imperata Cylindrica (+)-Xylarenal A Limonoid (tetranortriterpenoid) (-)-Oleocanthal (-)-Melotenine A Aaptos ciliata

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