Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 15, Pages 1530-1531Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b617537f
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Funding
- Biotechnology and Biological Sciences Research Council [BB/C504751/1] Funding Source: Medline
- Wellcome Trust Funding Source: Medline
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Enantioselective oxidation of racemic O-methyl-N-hydroxy-cyclohexylethylamine, using a variant of monoamine oxidase N (MAO-N) from Aspergillus niger, yields unreacted (R)-enantiomer (e.e. = 99%) together with the oxime exclusively in the (E)-configuration.
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