90105-50-3Relevant academic research and scientific papers
Stereoselective Reduction of Prochiral Cyclic 1,3-Diketones Using Different Biocatalysts
Contente, Martina Letizia,Dall’Oglio, Federica,Annunziata, Francesca,Molinari, Francesco,Rabuffetti, Marco,Romano, Diego,Tamborini, Lucia,Rother, D?rte,Pinto, Andrea
, p. 1176 - 1185 (2020)
We have developed biocatalytic methods for the stereoselective reduction of cyclic prochiral 1,3-diketones for the production of optically active β-hydroxyketones and/or 1,3-diols. The recombinant ketoreductase KRED1-Pglu (formulated as purified catalyst)
Asymmetric Microbial Reduction of Prochiral 2,2-Disubstituted Cycloalkanediones
Brooks, Dee W.,Mazdiyasni, Hormoz,Grothaus, Paul G.
, p. 3223 - 3232 (2007/10/02)
Asymmetric microbial reduction of a series of 2,2-disubstituted 1,3-cycloalkanediones with bakers' yeast was examined as an example of an enzyme-catalyzed distinction of a substrate containing two trigonal carbonyl centers with stereoheterotropic faces an
CHIRAL CYCLOHEXANOID SYNTHETIC PRECURSORS VIA ASYMMETRIC MICROBIAL REDUCTION OF PROCHIRAL CYCLOHEXANEDIONES
Brooks, Dee W.,Mazdiyasni, Hormoz,Chakrabarti, Sharmistha
, p. 1241 - 1244 (2007/10/02)
Microbial reduction of various 2,2-disubstituted-1,3-cyclohexanediones with bakers' yeast provides efficient access to chiral cyclohexanoid synthetic precursors.
