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    Asymmetric Synthetic Methodology
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      • Publisher's listprice GBP 190.00
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        96 159 Ft (91 580 Ft + 5% VAT)
      • Discount 20% (cc. 19 232 Ft off)
      • Discounted price 76 927 Ft (73 264 Ft + 5% VAT)

    96 159 Ft

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    Estimated delivery time: In stock at the publisher, but not at Prospero's office. Delivery time approx. 3-5 weeks.
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    Product details:

    • Edition number 1
    • Publisher CRC Press
    • Date of Publication 21 November 1995

    • ISBN 9780849389429
    • Binding Hardback
    • No. of pages512 pages
    • Size 254x178 mm
    • Weight 1090 g
    • Language English
    • Illustrations 29 Tables, black & white
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    Short description:

    This comprehensive text presents a critical discussion of the scopes and limitations of various organic synthetic methodologies that are available for performing asymmetric transformations

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    Long description:

    This comprehensive text presents a critical discussion of the scopes and limitations of various organic synthetic methodologies that are available for performing asymmetric transformations. In addition to purely chemical methods, the book covers applications of new enzymes and other biological systems that are increasingly useful in asymmetric methodology.

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    Table of Contents:

    IntroductionNomenclatureWhy Asymmetric Synthesis?Methods to Achieve Asymmetric SynthesisResolutionA Question of ScaleGeneral RulesCarbonyl AdditionsHouk's RuleAllylic StrainBaldwin's RulesPericyclic Transition StatesOne-Carbon TransformationsInversions at a Single Carbon CenterChiral Organometallic ReagentsOther ReactionsReactions With Carbonyl CompoundsReactions of Carbonyl Compounds With NucleophilesAcetal ReactionsOther ElectrophilesOther ReactionsReductionsEnolate Reactions of Carbonyl CompoundsEnol Ethers and Enolate FormationReactions of Enol Ethers and EnolatesUse of Nitrogen DerivativesAsymmetric Deprotonations and ProtonationsReactions of Functionalized Carbonyl SystemsAlkylations of 1,2-Functionalized Carbonyl CompoundsReductions of 1,2-Functionalized Carbonyl CompoundsAlkylations of 1,3-Functionalized Carbonyl CompoundsReductions of 1,3-Functionalized Carbonyl CompoundsOther SystemsAldol and Related ReactionsThe Aldol Reaction: Methods of ControlThe Aldol Reaction: The Role of Enolate Geometry and Metal CounterionThe Formose ReactionPreparation and Reactions of AlkenesAlkene SynthesisReactions of AlkenesReactions of Functionalized AlkenesHydrogenationsOther Transition Metal Catalyzed ReactionsHydride Delivery AgentsReactions of Some Functionalized AlkenesConjugate AdditionsAllyl AlkylationsOther ReactionsAsymmetric Oxidations of Isolated AlkenesEpoxidationsReactions of Epoxides1,2-DiolsFormation and Reactions of Cyclic SulfatesPreparation and Reactions of AziridinesOxidations of Functionalized AlkenesEpoxidation of Allyl AlcoholsReactions of 2,3-Epoxy Alcohols and Related SystemsEpoxidations and Reactions of Other Unsaturated SystemsOther OxidationsOther SystemsPericyclic ReactionsThe Diels-Alder ReactionClaisen

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    Asymmetric Synthetic Methodology

    Asymmetric Synthetic Methodology

    Ager, David John; East, Michael B.;

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