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Recent Advances in the Direct Nucleophilic Substitution of Allylic Alcohols through SN1-Type Reactions
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2013
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Cross-coupling ReactionAllylic Alcohols 2.1New Allylic CompoundsEngineeringNatural SciencesDiversity-oriented SynthesisCatalytic SynthesisAllylic AlcoholsOrganic ChemistryOrganometallic CatalysisCatalysisMolecular CatalysisChemistryAsymmetric CatalysisRecent AdvancesEnantioselective SynthesisBiomolecular EngineeringDirect Nucleophilic Substitution
Direct nucleophilic substitution reactions of allylic alcohols are environmentally friendly, since they generate only water as a byproduct, allowing access to new allylic compounds. This reaction has, thus, attracted the interest of the chemical community and several strategies have been developed for its successful accomplishment. This review gathers the latest advances in this methodology involving S<sub>N</sub>1-type reactions. 1 Introduction 2 S<sub>N</sub>1-Type Direct Nucleophilic Substitution Reactions of Allylic Alcohols 2.1 Lewis Acids as Catalysts 2.2 Brønsted Acids as Catalysts 2.3 Other Promoters 3 Conclusions and Outlook