Saltar al contenido
Merck

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
RESUMEN

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.

MATERIALES
Número de producto
Marca
Descripción del producto

Sigma-Aldrich
Azobisisobutyronitrile, 12 wt. % in acetone
Sigma-Aldrich
2,2′-Azobis(2-methylpropionitrile), recrystallized from methanol, 99%
Sigma-Aldrich
2,2′-Azobis(2-methylpropionitrile) solution, 0.2 M in toluene