Publication | Closed Access
The Trityl Cation Catalyzed Michael Type Reaction of Stannylated Nucleophiles with Ethylthioketene Dithioacetals
14
Citations
7
References
1987
Year
Cross-coupling ReactionEngineeringCatalytic AmountEthylthioketene DithioacetalsNatural SciencesDiversity-oriented SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisSynthetic ChemistryChemistryTrityl SaltAsymmetric CatalysisSynthetic EquivalentStannylated NucleophilesEnantioselective SynthesisBiomolecular Engineering
Abstract In the presence of a catalytic amount of trityl salt, allylstannanes and stannylated enolates smoothly react with 2-(2-ethylthioalkylidene)-1,3-dithiolane, synthetic equivalent of α,β-unsaturated ester, to afford the corresponding adducts in good yields, respectively.
| Year | Citations | |
|---|---|---|
Page 1
Page 1