142696-01-3Relevant articles and documents
Lipase-catalyzed kinetic resolution of (+/-)-cis-flavan-4-ol and its acetate: synthesis of chiral 3-hydroxyflavanones.
Todoroki, Tamotsu,Saito, Akiko,Tanaka, Akira
, p. 1772 - 1774 (2002)
Lipase-catalyzed kinetic resolution of (+/-)-cis-flavan-4-ol and its acetate led to enantiomerically enriched flavan-4-ol and its acetate. These chiral compounds were converted to (2R, 3R)- and (25, 3S)-3-hydroxyflavanones.
Enzymatic Kinetic Resolution of Flavanone and cis-4-Acetoxyflavan
Izumi, Taeko,Hino, Toshimi,Kasahara, Akira
, p. 1265 - 1268 (2007/10/02)
The microbial, asymmetric reduction of flavanone with fermenting bakers' yeast led to the formation of (2S,4S)-(+)-cis-4-hydroxyflavan and (2R)-(+)-flavanone.The kinetic resolution of racemic cis-4-acetoxyflavan with lipase PS yields (2R,4R)-(-)-cis-4-hydroxyflavan, and the (2S,4S)-(+)-enantiomer remains as the acetate.