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enzyme catalysis (4) 4
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imine reductase (4) 4
chemistry, physical (3) 3
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ChemCatChem, ISSN 1867-3880, 01/2018, Volume 10, Issue 1, pp. 183 - 187
In the last years, imine reductases (IREDs) have gained importance for the formation of chiral amines by catalyzing asymmetric reductions of imines and chemo‐... 
site-directed mutagenesis | activity recovery | enzyme catalysis | cofactor specificity | imine reductase | NADPH | IREDS | CATALYZED ORGANIC-SYNTHESIS | REGENERATION | CHEMISTRY, PHYSICAL | PHOSPHITE DEHYDROGENASE | CHIRAL AMINES | FORMATE DEHYDROGENASE | AMINATION | ENZYME | RATIONAL DESIGN | Schiff bases | Enzymes | Chemotherapy | Catalysis | Analysis | Cancer
Journal Article
ChemCatChem, ISSN 1867-3880, 01/2018, Volume 10, Issue 1, pp. 3 - 3
The Cover Feature shows the switch of the cofactor specificity of an imine reductase from NADPH to NADH. In their Full Paper, N. Borlinghaus and B. M. Nestl... 
site-directed mutagenesis | activity recovery | enzyme catalysis | cofactor specificity | imine reductase
Journal Article
ISSN 1463-9262, 3/2019, Volume 21, Issue 6, pp. 1396 - 14
Herein, we report an enzymatic cascade involving an oxidase, an imine reductase and a hydrogenase for the H 2 -driven synthesis of N -heterocycles. Variants of... 
Journal Article
Green Chemistry, ISSN 1463-9262, 03/2019, Volume 21, Issue 6, pp. 1396 - 1400
Herein, we report an enzymatic cascade involving an oxidase, an imine reductase and a hydrogenase for the H2-driven synthesis of N-heterocycles. Variants of... 
Journal Article
ACS Catalysis, ISSN 2155-5435, 04/2018, Volume 8, Issue 4, pp. 3727 - 3732
Given the widespread importance of piperazines as building blocks for the production of pharmaceuticals, an efficient and selective synthesis is highly... 
enantioselectivity | IMINE REDUCTASES IREDS | double reductive amination | imine reductase | HYDROGENATION | REAGENTS | CHEMISTRY, PHYSICAL | N- and C-substituted heterocycles | KETONES | HERQULINE | substrate scope | piperazines | REDUCTIVE AMINATION | ALKALOIDS
Journal Article
Green Chemistry, ISSN 1463-9262, 01/2019, Volume 21, Issue 6, pp. 1396 - 1400
Herein, we report an enzymatic cascade involving an oxidase, an imine reductase and a hydrogenase for the H2-driven synthesis of N-heterocycles. Variants of... 
Hydrogenase | Diamines | Synthesis | Oxidase | Rhodococcus | Putrescine oxidase | Selectivity | NADP | Putrescine | Substrates | Reductase
Journal Article
ChemCatChem, ISSN 1867-3880, 12/2019, Volume 11, Issue 23, pp. 5738 - 5742
Synthesis of 3‐methylpiperidine from 1,5‐diamino‐2‐methylpentane in preparative scale is reported by using recombinant Escherichia coli cells expressing a... 
amine oxidase | imine reductase | whole cell enzyme cascade | methylpiperidine | upscaling
Journal Article
Green Chemistry, ISSN 1463-9262, 2019, Volume 21, Issue 6, pp. 1396 - 1400
Herein, we report an enzymatic cascade involving an oxidase, an imine reductase and a hydrogenase for the H-2-driven synthesis of N-heterocycles. Variants of... 
PUTRESCINE OXIDASE | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | IMINE | TOOLBOX | ENZYMES | WELL | ASYMMETRIC REDUCTION | BIOCATALYST | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
ChemCatChem, ISSN 1867-3880, 05/2016, Volume 8, Issue 9, pp. 1636 - 1640
The Wittig‐type carbonyl olefination reaction has no biocatalytic equivalent. To build complex molecular scaffolds, however, C−C bond‐forming reactions are... 
C−C bond formation | enzyme catalysis | Wittig reactions | biocatalysis | olefination | C-C bond formation | COMPLEX | CHEMISTRY, PHYSICAL | ALDEHYDES | SQUALENE HOPENE CYCLASES | EFFICIENT | Enzymes | Catalysis | Aldehydes | Escherichia coli | Heme
Journal Article
World journal of microbiology & biotechnology, 10/2017, Volume 33, Issue 11, p. 199
Imine reductases are nicotinamide-dependent enzymes that catalyze the asymmetric reduction of various imines to the corresponding amine products. Owing to the... 
Journal Article
ChemCatChem, ISSN 1867-3880, 05/2016, Volume 8, Issue 9, pp. 1636 - 1640
Journal Article
ChemCatChem, ISSN 1867-3880, 05/2016, Volume 8, Issue 9, pp. 1747 - 1747
The Cover shows an enzymatic carbonyl olefination reaction in E.coli where the corresponding enzyme—depicted as the clownfish nemo—has to be found in the... 
C−C bond formation | enzyme catalysis | Wittig reactions | biocatalysis | olefination
Journal Article
ChemistrySelect, ISSN 2365-6549, 05/2016, Volume 1, Issue 6, pp. 1243 - 1251
Journal Article
ChemistrySelect, ISSN 2365-6549, 05/2016, Volume 1, Issue 6, pp. 1243 - 1251
The native redox partners of many novel cytochrome P450 monooxygenases (CYPs) are unknown. Therefore, they are combined with non‐native redox partners to... 
redox partner | reductase | redox partner interaction site | CYP | Cytochrome P450 | RECOGNITION | DIRECTED MUTAGENESIS | IDENTIFICATION | CHEMISTRY, MULTIDISCIPLINARY | MUTANTS | ELECTRON-TRANSFER | HEME | STRUCTURAL BASIS | SURFACE | BINDING-SITE | P450
Journal Article
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