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Highly Stereoselective Conjugate Addition and α‐Alkynylation Reaction with Electron‐Deficient Alkynes Catalyzed by Chiral Scandium(III) Complexes
43
Citations
52
References
2013
Year
Asymmetric CatalysisChemical EngineeringScandium ComplexesEngineeringAlkene MetathesisCross-coupling ReactionNovel OrganocatalystsChiral ScandiumOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryUnstable Z-olefin DerivativesStereoselective Conjugate Additionα‐Alkynylation Reaction3-Substituted OxindolesEnantioselective Synthesis
The highly Z-selective asymmetric conjugate addition of 3-substituted oxindoles to alkynyl carbonyl compounds has been developed by using scandium complexes of chiral N,N'-dioxides under mild conditions. The thermodynamically unstable Z-olefin derivatives were obtained in excellent yields and high enantiomeric and geometric control. The catalyst was also found to be effective in the asymmetric acetylenic substitution reaction of 3-substituted oxindoles, giving excellent enantioselectivities.
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