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Biocatalytic Reduction Reactions from a Chemist's Perspective
Frank Hollmann1,2, Diederik J Opperman2, Caroline E Paul1
1Department of Biotechnology, Delft University of Technology, Van der Maasweg 9, 2629 HZ, Delft, The Netherlands.
Enzymatic reductions offer selective and efficient routes in organic synthesis for chiral compounds. This review covers enzymes catalyzing various reductions, including carbonyl and reductive aminations.
Area of Science:
- Organic Chemistry
- Biocatalysis
- Synthetic Chemistry
Background:
- Reductions are fundamental transformations in organic synthesis.
- Enzymatic catalysis offers high selectivity (stereo-, regio-, chemo-) for reduction reactions.
- Enzymes provide greener and potentially shorter synthetic pathways.
Purpose of the Study:
- To review the current state-of-the-art in enzymatic reductions.
- To highlight the potential of enzymes in catalyzing diverse reduction reactions.
- To cover a range of enzymatic reduction types, including carbonyl, enone, aromatic reductions, and reductive aminations.
Main Methods:
- Literature review of enzymatic reduction studies.
- Analysis of enzyme classes and their catalytic mechanisms for reductions.
- Compilation of examples showcasing enzyme applications in synthesis.
Main Results:
- Enzymes demonstrate remarkable selectivity in catalyzing reductions.
- Enzymatic routes can be competitive with or superior to classical methods.
- A broad spectrum of reduction reactions can be achieved using enzymes.
Conclusions:
- Enzymatic reductions are powerful tools for producing chiral molecules.
- Enzymes offer sustainable and efficient alternatives for synthesizing valuable compounds.
- The scope of enzymatic reductions continues to expand, impacting both fine chemicals and bulk chemical production.
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