NAD(P)h-independent asymmetric C=C bond reduction catalyzed by ene reductases by using artificial co-substrates as the hydrogen donor

Chemistry - A European Journal

Volumn 20, Issue 5, 2014, Pages 1403-1409

  Winkler, Christoph K ^a   Clay, Dorina ^a   Entner, Marcello ^a   Plank, Markus ^a   Faber, Kurt ^a  

^a UNIVERSITY OF GRAZ   (Austria)

Author keywords

Alkene reduction; Artificial biocatalysis; Ene reductases; Enzyme catalysis; Hydrogen donors

Indexed keywords

AMIDES; CATALYSIS; ENZYMES; HYDROGEN; HYDROGEN BONDS;

ASYMMETRIC BIOREDUCTION; BIOCATALYSIS; ENE REDUCTASES; ENZYME CATALYSIS; HYDROGEN DONOR; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATES; OPTIMIZED CONDITIONS; RECYCLING SYSTEMS;

REDUCTION;

BIOMATERIAL; CARBON; HYDROGEN; NICOTINAMIDE ADENINE DINUCLEOTIDE; OXIDOREDUCTASE;

ALKENE REDUCTION; ARTICLE; ARTIFICIAL BIOCATALYSIS; BIOCATALYSIS; CHEMISTRY; ENE REDUCTASES; ENZYME CATALYSIS; ENZYME SPECIFICITY; HYDROGEN DONORS; METABOLISM; OXIDATION REDUCTION REACTION; STEREOISOMERISM;

ALKENE REDUCTION; ARTIFICIAL BIOCATALYSIS; ENE REDUCTASES; ENZYME CATALYSIS; HYDROGEN DONORS;

BIOCATALYSIS; BIOCOMPATIBLE MATERIALS; CARBON; HYDROGEN; NAD; OXIDATION-REDUCTION; OXIDOREDUCTASES; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 84895928265     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201303897     Document Type: Article

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