Publication | Closed Access
Bimetallic Catalytic Asymmetric Tandem Reaction of β‐Alkynyl Ketones to Synthesize 6,6‐Spiroketals
26
Citations
57
References
2019
Year
Enantioselective SynthesisEngineeringNatural SciencesEnantioselective Tandem ReactionDiversity-oriented SynthesisStraightforward Accessβ‐Alkynyl KetonesOrganic ChemistryCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisCatalytic CycleBiomolecular Engineering
Abstract The enantioselective tandem reaction of β,γ‐unsaturated α‐ketoesters with β‐alkynyl ketones was realized by a bimetallic catalytic system of achiral Au ΙΙΙ salt and chiral N , N ′‐dioxide‐Mg ΙΙ complex. The cycloisomerization of β‐alkynyl ketone and asymmetric intermolecular [4+2] cycloaddition with β,γ‐unsaturated α‐ketoesters subsequently occurred, providing an efficient and straightforward access to chiral multifunctional 6,6‐spiroketals in up to 97 % yield, 94 % ee and >19/1 d.r. Besides, a catalytic cycle was proposed based on the results of control experiments.
| Year | Citations | |
|---|---|---|
Page 1
Page 1