Publication | Closed Access
Chiral Sulfoxides as Neutral Coordinate-Organocatalysts in Asymmetric Allylation of <i>N</i>-Acylhydrazones Using Allyltrichlorosilanes
186
Citations
10
References
2003
Year
Asymmetric CatalysisActive Chiral SulfoxidesNovel OrganocatalystsAsymmetric AllylationEngineeringNeutral Coordinate-organocatalystsBiochemistryNatural SciencesEffective Neutral Coordinate-organocatalystsOrganic ChemistryStereoselective SynthesisChemistryHigh EnantioselectivityChiral SulfoxidesEnantioselective SynthesisBiomolecular Engineering
Sulfoxides were first introduced to the allylation of N-acylhydrazones with allyltrichlorosilanes as effective neutral coordinate-organocatalysts (NCOs). Both high diastereo- and enantioselectivity were attained when optically active chiral sulfoxides were used. Asymmetric crotylations using (Z)- and (E)-crotyltrichlorosilanes showed a high level of stereospecificity (Z --> anti and E --> syn) with high enantioselectivity.
| Year | Citations | |
|---|---|---|
Page 1
Page 1