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  • Switching from (R)- to (S)-selective chemoenzymatic DKR of amines involving sulfanyl radical-mediated racemization.

Switching from (R)- to (S)-selective chemoenzymatic DKR of amines involving sulfanyl radical-mediated racemization.

Organic & biomolecular chemistry (2010-07-28)
Lahssen El Blidi, Nicolas Vanthuyne, Didier Siri, Stéphane Gastaldi, Michèle P Bertrand, Gérard Gil
ZUSAMMENFASSUNG

Chemoenzymatic dynamic kinetic resolution (DKR) of amines involving sulfanyl radical-induced racemization happened to be the very first switchable DKR process allowing the synthesis of either (R)- or (S)-amides, in good yield and high enantiomeric excess, depending on the nature of the enzyme; the different steps of the development of (S)-selective DKR are discussed.

MATERIALIEN
Produktnummer
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Produktbeschreibung

Sigma-Aldrich
2,2′-Azobis(2-Methylpropionitril), 98%
Sigma-Aldrich
AIBN -Lösung, 0.2 M in toluene
Sigma-Aldrich
2,2′-Azobis(2-Methylpropionitril), purum, ≥98.0% (GC)