Organic Letters · 2002 · 45 citations · 15 references
Asymmetric CatalysisChemical EngineeringCorresponding ThiolateEngineeringNovel ApproachSulfide PrecursorOrganic ChemistrySulfenate AnionsCatalysisStereoselective SynthesisChemistryEnantioenriched SulfoxidesNatural Product SynthesisSulfenate AnionSynthetic ChemistryEnantioselective Synthesis
[reaction: see text] Efficient 1,4-asymmetric induction with an enantiopure aminoalkyl group as the chiral auxiliary has been achieved in the first example of diastereoselective alkylation (up to 98:2) of a sulfenate anion, readily prepared by oxidation of the corresponding thiolate. The stereochemistry of the sulfoxide produced is the opposite of that obtained by the conventional route based on oxidation of the sulfide precursor.
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Eusebio Juaristi, José Luis León-Romo, Adelfo Reyes et al. · Tetrahedron Asymmetry · 1999 · 170 citations
Engineering, Organic Chemistry, Stereoselective Synthesis +8
Eusebio Juaristi, Jaime Escalante, José Luis León-Romo et al. · Tetrahedron Asymmetry · 1998 · 148 citations