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    Indole Alkaloids

    Indole Alkaloids

    - Spirooxindole

    Af +1
    Bog E-bog
    • Format
    • Bog, paperback
    • Engelsk

    Beskrivelse

    Indole Alkaloids: Spirooxindole details the multistep synthesis of natural products using schematic diagrams, providing a quick-and-easy way to review and understand new and novel synthetic strategies to construct structural frameworks of natural products. As a volume in the Visual Guides to Natural Product Synthesis series, this book presents the schematic total syntheses of natural products containing a “spirooxindole” core structure. It covers spirooxindole molecules through visual diagrams, highlighting key steps involved in total, formal and semi-syntheses. Sections cover Brevianamide A and B, Citrinadin A and B, Coerulescine and Horsfiline, Elacomine and Isoelacomine, Gelsemine, Paraherquamide A and B, Rynchophylline, Isorynchophylline, and more. Visual layouts provide quick-and- easy access to developed synthetic routes towards the targeted spirooxindoles.

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    Detaljer
    Størrelse og vægt
  • Vægt390 g
    • coffee cup img
    10 cm
    book img
    15,2 cm
    22,9 cm

    Forfattere

    Maliha Uroos Abdul Hameed Sadia Naz Muhammad Raza Shah

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    Asymmetric synthesis Claisen rearrangement Heck reaction Carreira Cross Metathesis Hydrogenolysis Diketopiperazine Asymmetric Carbamoylation Chiral auxiliary 12-epi-Spirotryprostatin B 2+2 photocycloaddition 3+2 Annulation 5-exo cyclization 8-phenylmenthol 3-Dipolar Cycloaddition 3+2 cycloaddition Aminal urethane Austamide Asymmetric Allylic Alkylation (-)-Affinisine Asymmetric nitroolefination Aza-Michael initiated ring closure (aza-MIRC) Ban’s intermediate Amide coupling Beckmann Rearrangement Barton-modified Hunsdiecker protocol Bosch chiral lactam Chiral Bronsted acid Citrinadin A Citrinadin B Carreira’s diastereoselective 3+2 annulation Claisen Condensation Azomethine ylides Corynoxeine Dieckmann-condensation Dieckmann cyclization Corey–Chaykovsky epoxidation Brevianamide A Brevianamide B Cross-dehydrogenative coupling (CDC) Cycloisomerization Brevianamide C Butenylation Carboline Carbomagnesation Deformylation enantioselective Chemoselective Eschweiler–Clarke Curtius rearrangement DMDO-mediated oxidative rearrangement Elacomine ?(E)-dienoate Fischer-indole synthesis Coerulescine Dihydrosecologanin aglycone Convergent selective annulation reaction Formal synthesis Heptacycle Cyclopropanation Hydrogenolysis deprotection Davis’ oxaziridine Dehydrobrevianamide E Heck cyclization Dehydrospiropyrrolidine Dihydrocorynantheine Dihydrospirotryprostatin B Intramolecular SN2 displacement Diazo Transfer Hynchophyline Horner–Wordsworth–Emmons reaction Horsfiline Intramolecular iminium ion spirocyclization Ellman imine Ender’s epoxidation Enone lactam Lactamization Enantioelective Mannich spirocyclization Intramolecular lactamization Intramolecular oxymercuration Isorhynchophyline Knoevengel condensation Gassman oxindole synthesis Marcfortine A Mannich–Michael addition Gramine Heck cyanation Gelsemine Horner–Wordsworth–Emmons Intramolecular cyclization Julia–Kocienski olefination Isorhynchophylline L-proline Intermolecular 3+2 nitrone cycloaddition Isoelacomine

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