Strategies and Tactics in Organic Synthesis

- Volume 8

Forfatter: info mangler
Bog
  • Format
  • Bog, hardback
  • Engelsk

Beskrivelse

A classic in the area of organic synthesis, Strategies and Tactics in Organic Synthesis provides a forum for investigators to discuss their approach to the science and art of organic synthesis. Rather than a simple presentation of data or a second-hand analysis, this book vividly demonstrates through first hand accounts how synthesis is really done and how by discovering new reactions, creating new designs and building molecules with atom and step economies, the advancement of the science of organic synthesis is providing solutions through function to create a better world.

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Detaljer
  • SprogEngelsk
  • Sidetal460
  • Udgivelsesdato03-08-2012
  • ISBN139780123865403
  • Forlag Academic Press Inc
  • FormatHardback
Størrelse og vægt
  • Vægt860 g
  • coffee cup img
    10 cm
    book img
    15,2 cm
    22,9 cm

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    Oxidation Glycosylation Biosynthesis Radicals Alkanes Claisen rearrangement Palladium Computations Asymmetric Allylation Alder Ene Reaction Mechanisms Cross Metathesis Cycloaddition Antibiotic Ring-closing Metathesis CH activation Triterpene Total Synthesis Piperidines Natural product Carbamate Natural product synthesis Polyketide Diamondoids Rearrangement Biomimetic Biomimetic synthesis Antifungal activity Atropisomerism Anticancer Enantioselective epoxidation Site-selective Functionalization Tetrahydropyran Oxidations Sulfone Borane Marine natural product Macrocyclization Selenides 2-metallate rearrangement 5-epi-vibsanin E acyclic stereocontrol allylboration 4-diol allylic transposition aminopyranose Antitumor Terpenoid ansa-compound Allylsilane Aminoimidazoles anchimeric assistance aiglialomycin antitumor antibiotic borylated alkyne boronic ester Baylis-Hillman reaction carbonyl ylide chelation-controlled reduction Chiral Bases copper hydride C-arylglycoside enantioselective enantioselective Lewis-base catalysis dianion oxidation Chemoselective Alcohol Oxidation chemobiosynthesis cross-metathesis (11 key words) Dipolar cycloaddition Eremanthus elaeagnus Evans aldol reaction Conjugate Addition Grignard exchange dianion structure diazabicyclo[3.2.1]octane Ireland-Claisen rearrangement Electrophiles π-allyl etherification Enolate C-Acylation Lycopodium alkaloids Macrocyclic Aldol Reaction Macrolactone Macrolides marine alkaloid natural product total synthesis glycosyloxyacetaldehyde Negishi cross-coupling halichlorine rhodium carbene pseudolaric acid photo-Fries reaction Rhenium Oxide regioselective epoxidation Ramberg-Backlund Rearrangement reductive aldol stereospecific oxacyclization solandelactone Hiyama-Denmark reaction tetrahydroisoquinoline squalene epoxides terrestrial natural product lyconadin A vinylboronates organosilicon cross-coupling palladium-catalyzed cross-coupling Oppolzer's Sultam papulacandin SN2′ displacement radical cyclization Sponge metabolites Suzuki cross-coupling Quinone methide vibsane natural products stereospecific rearrangement vibsanin E

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