FIELD: biotechnology, biochemistry. SUBSTANCE: method involves usage of 2-aminopropane as a donor of amino-group in stereoselective synthesis of chiral amine from ketone using transaminase. In part, (S)-1-methoxy-2-aminopropane is prepared by contacting methoxyacetone with transaminase in the presence of 2- aminopropane. Reaction is carried out up to the significant conversion of methoxyacetone to (S)-1-methoxy-2-aminopropane and conversion of 2-aminopropane to acetone. Then (S)-1-methoxy-2- aminopropane is isolated. Method provides reduction of energy and working consumptions and enhanced yield of chiral amine. EFFECT: improved preparing method. 3 cl, 5 ex
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METHOD OF ENANTIOMERIC ENRICHMENT OF A MIXTURE CONSISTING OF TWO ENANTIOMERIC CHIRAL AMINES |
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|
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