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Hybrid Metal/Organo Relay Catalysis Enables Enynes To Be Latent Dienes for Asymmetric Diels–Alder Reaction
168
Citations
51
References
2012
Year
Chiral N-triflyl PhosphoramideAsymmetric CatalysisCross-coupling ReactionEngineeringAlkene MetathesisNatural SciencesDiversity-oriented SynthesisAsymmetric Diels–alder ReactionHybrid AuOrganic ChemistryLatent 1,3-SilyloxydienesCatalysisOrganometallic CatalysisChemistryLatent DienesEnantioselective SynthesisBiomolecular Engineering
The hybrid Au(I)/Brønsted acid binary catalyst system enables enynes to serve as latent 1,3-silyloxydienes capable of participating in the first cascade hydrosiloxylation of an enynyl silanol/asymmetric Diels-Alder reaction. A variety of polycyclic compounds bearing multistereogenic centers were obtained in high yields and excellent enantioselectivities from the relay catalytic cascade reaction between (2-(but-3-en-1-ynyl)phenyl) silanols and quinones catalyzed by the combined achiral gold complex and chiral N-triflyl phosphoramide.
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