Nicotinamide-independent asymmetric bioreduction of C Created by potrace 1.16, written by Peter Selinger 2001-2019 C-bonds via disproportionation of enones catalyzed by enoate reductases
The asymmetric bioreduction of activated C C-bonds catalyzed by a single flavoprotein was achieved via direct hydrogen transfer from a sacrificial 2-enone or 1,4-dione as hydrogen donor without requirement of a nicotinamide cofactor. Due to its simplicity, this system has clear advantages over conve...
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Published in | Tetrahedron Vol. 66; no. 3-2; pp. 663 - 667 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Pergamon Press
16.01.2010
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Online Access | Get full text |
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Abstract | The asymmetric bioreduction of activated C
C-bonds catalyzed by a single flavoprotein was achieved via direct hydrogen transfer from a sacrificial 2-enone or 1,4-dione as hydrogen donor without requirement of a nicotinamide cofactor. Due to its simplicity, this system has clear advantages over conventional FAD-recycling systems. |
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AbstractList | The asymmetric bioreduction of activated C
C-bonds catalyzed by a single flavoprotein was achieved via direct hydrogen transfer from a sacrificial 2-enone or 1,4-dione as hydrogen donor without requirement of a nicotinamide cofactor. Due to its simplicity, this system has clear advantages over conventional FAD-recycling systems. |
Author | Stueckler, Clemens Reiter, Tamara C. Baudendistel, Nina Faber, Kurt |
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Copyright | 2010 Elsevier Ltd. 2009 Elsevier Ltd |
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C-bonds catalyzed by a single flavoprotein was achieved via direct hydrogen transfer from a sacrificial 2-enone or... |
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Title | Nicotinamide-independent asymmetric bioreduction of C Created by potrace 1.16, written by Peter Selinger 2001-2019 C-bonds via disproportionation of enones catalyzed by enoate reductases |
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