1453201-18-7Relevant articles and documents
Highly enantioselective reduction of α-methylated nitroalkenes
Burda, Edyta,Re?, Tina,Winkler, Till,Giese, Carolin,Kostrov, Xenia,Huber, Tobias,Hummel, Werner,Gr?ger, Harald
, p. 9323 - 9326 (2013/09/12)
Highly selective: The reduction of α-methyl-substituted nitroalkenes succeeds in a highly enantioselective fashion with an ene reductase from Gluconobacter oxydans. Under optimized reaction conditions the desired nitroalkanes are formed with enantiomeric excesses of up to 95% in these biotransformations. Copyright