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Asymmetric Allylic Alkylation, an Enabling Methodology

The Journal of Organic Chemistry · 2004 · Vol. 69(18) · pp. 5813–5837
Barry M. Trost

Abstract

The diversity of mechanisms for enantiodiscrimination and of bond types that can be formed make Pd-catalyzed asymmetric allylic alkylation a powerful key step for simplification of synthetic strategy to complex molecular targets. Using a wide range of different classes of compounds including alkaloids, polyhydrofurans, nucleosides and carbanucleosides, cyclohexitols and cyclopentitols, chromanes, cyclopentanoids, amino acids, barbiturates, etc., novel synthetic strategies emerge that provide short efficient asymmetric syntheses.

Asymmetric Synthesis and CatalysisChemical Synthesis and AnalysisSynthetic Organic Chemistry MethodsChemistryTsuji–Trost reactionAlkylationCombinatorial chemistryAllylic rearrangementOrganic chemistryStereochemistryCatalysis

MeSH terms

AlkaloidsAlkylationAllyl CompoundsBiological FactorsCatalysisModels, ChemicalPalladiumStereoisomerismMolecular Structure
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