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Synthetically Useful Reactions of Epoxides

Synthesis · 1984 · Vol. 1984(08) · pp. 629–656
Janice Smith

Abstract

The synthetically useful reactions of epoxides are reviewed in this article. An emphasis is placed on methods which have recently been reported in the literature. 1. Introduction 2. Reaction of Epoxides with Nucleophiles 2.1. General Considerations 2.2. Ring Opening of Epoxides with Heteroatomic Nucleophiles 2.3. Ring Opening of Epoxides with Carbon Nucleophiles 2.4. Intramolecular Ring Opening of Epoxides 3. Rearrangement of Epoxides to Carbonyl Compounds 4. Rearrangement of Epoxides to Allylic Alcohols 5. Deoxygenation of Epoxides to Olefins 6. Reduction of Epoxides to Alcohols 7. Epoxides with Adjacent Functional Groups 7.1. Monoepoxides of 1,3-Dienes 7.2. α,β-Epoxyketones 7.3. α,β-Epoxysilanes 8. Conclusions

Chemical Synthesis and ReactionsOrganic Chemistry Cycloaddition ReactionsSynthetic Organic Chemistry MethodsChemistryNucleophileDeoxygenationEpoxideRing (chemistry)Intramolecular forceAllylic rearrangementOrganic chemistryMedicinal chemistryCatalysis
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Cited by
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