Publication | Closed Access
Cooperative Catalysis for the First Asymmetric Formal [3+2] Cycloaddition Reaction of Isocyanoacetates to α,β‐Unsaturated Ketones
86
Citations
40
References
2011
Year
Silver NitrateCross-coupling ReactionNovel OrganocatalystsEngineeringDiversity Oriented SynthesisNatural SciencesBifunctional RoleDiversity-oriented SynthesisCooperative CatalysisOrganic ChemistryCycloaddition ReactionOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
Abstract A cooperative multicatalytic cascade sequence involving isocyanoacetates and α,β‐unsaturated ketones is described for the enantioselective synthesis of 2,3‐dihydropyrroles. The key to promoting the multistep asymmetric reaction is the combination of cinchona alkaloid derived organocatalysts with silver nitrate. Merging both organic and metal catalytic cycles enables the formation of two C–C bonds and the generation of a stereogenic center in a single process. The study has also shown that the bifunctional role of the organocatalyst is crucial for the asymmetric version of the cycloaddition reaction.
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