Artículos de revistas
Bioreduction of alpha-haloacetophenones by Rhodotorula glutinis and Geotrichum candidum
Registro en:
Arkivoc. Arkat Usa Inc, n. 404, n. 410, 2003.
1551-7012
WOS:000220556500038
Autor
Fardelone, LC
Rodrigues, JAR
Moran, PJS
Institución
Resumen
Enantioselective reductions with enantiocomplementarity of alpha-haloacetophenones by Rhodotorula glutinis CCT 2182 and Geotrichum candidum CCT 1205 afforded the corresponding (R)- and (S)-halohydrins (halo = Cl, Br and I), respectively, in high chemical yields (89-99%) and enantiomeric excesses (92-99%). These halohydrins are potential chiral building blocks for the stereoselective syntheses of valuable compounds. 10 404 410