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- W2101926836 endingPage "782" @default.
- W2101926836 startingPage "762" @default.
- W2101926836 abstract "Abstract Redox enzymes have tremendous potential as catalysts for preparative organic chemistry. Their usually high selectivity, paired with their catalytic efficiency under mild reaction conditions, makes them potentially very valuable tools for synthesis. The number of interesting monooxygenases, dehydrogenases, reductases, oxidases, and peroxidases is steadily increasing and the tailoring of a given biocatalyst is more and more becoming standard technology. However, their cofactor dependency still represents a major impediment en route to true preparative applicability. Currently, three different approaches to deal with this ‘cofactor challenge’ are being pursued: using whole cells, biomimetic approaches comprising enzymatic cofactor regenerations systems, and ‘unconventional’ nonenzymatic regeneration. The latter technique offers the promise of enabling simple, easily applicable, and robust reaction schemes, for example, by circumventing the ‘cofactor challenge’ and introducing redox power directly to the enzyme’s active sites." @default.
- W2101926836 created "2016-06-24" @default.
- W2101926836 creator A5028443868 @default.
- W2101926836 creator A5039285985 @default.
- W2101926836 creator A5046359505 @default.
- W2101926836 date "2010-07-07" @default.
- W2101926836 modified "2023-10-07" @default.
- W2101926836 title "Biocatalytic Redox Reactions for Organic Synthesis: Nonconventional Regeneration Methods" @default.
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