Enzymatic reductions for the chemist

F Hollmann, IWCE Arends, D Holtmann - Green Chemistry, 2011 - pubs.rsc.org
When challenged by a difficult reduction reaction, a chemist should always also consider
biocatalysis in synthesis planning. The inherent selectivity of enzymes has been known for …

Enantioselective enzymatic desymmetrizations in organic synthesis

E García-Urdiales, I Alfonso, V Gotor - Chemical Reviews, 2005 - ACS Publications
During the recent past years, tremendous efforts have been made to establish
enantioselective routes for the preparation of enantiomerically pure compounds due to their …

Cooperative asymmetric reactions combining photocatalysis and enzymatic catalysis

ZC Litman, Y Wang, H Zhao, JF Hartwig - Nature, 2018 - nature.com
Living organisms rely on simultaneous reactions catalysed by mutually compatible and
selective enzymes to synthesize complex natural products and other metabolites. To …

Biocatalytic reductions and chemical versatility of the old yellow enzyme family of flavoprotein oxidoreductases

HS Toogood, JM Gardiner, NS Scrutton - ChemCatChem, 2010 - Wiley Online Library
The old yellow enzyme (OYE) family is a large group of flavin‐dependent redox biocatalysts
with major applications in the industrial reduction of activated alkenes. These enzymes have …

Better than nature: nicotinamide biomimetics that outperform natural coenzymes

T Knaus, CE Paul, CW Levy, S De Vries… - Journal of the …, 2016 - ACS Publications
The search for affordable, green biocatalytic processes is a challenge for chemicals
manufacture. Redox biotransformations are potentially attractive, but they rely on unstable …

[PDF][PDF] How Green is Biocatalysis? To Calculate is To Know.

Y Ni, D Holtmann, F Hollmann - ChemCatChem, 2014 - researchgate.net
Green chemistry aims to minimize the environmental hazards of chemical processes and
their products. Ever since its introduction by Anastas,[1] this principle has inspired …

Enantioenriched compounds via enzyme-catalyzed redox reactions

M Hall, AS Bommarius - Chemical reviews, 2011 - ACS Publications
Redox reactions are essential to any currently known form of life and are at the core of a
majority of metabolic processes, such as cellular respiration or photosynthesis. As about …

[HTML][HTML] Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds

CK Winkler, G Tasnádi, D Clay, M Hall, K Faber - Journal of biotechnology, 2012 - Elsevier
Ene-reductases from the 'Old Yellow Enzyme'family of flavoproteins catalyze the asymmetric
reduction of various α, β-unsaturated compounds at the expense of a nicotinamide cofactor …

Enzymatic strategies for asymmetric synthesis

M Hall - RSC Chemical Biology, 2021 - pubs.rsc.org
Enzymes, at the turn of the 21st century, are gaining a momentum. Especially in the field of
synthetic organic chemistry, a broad variety of biocatalysts are being applied in an …

Old yellow enzyme-catalysed asymmetric hydrogenation: linking family roots with improved catalysis

A Scholtissek, D Tischler, AH Westphal… - Catalysts, 2017 - mdpi.com
Asymmetric hydrogenation of activated alkenes catalysed by ene-reductases from the old
yellow enzyme family (OYEs) leading to chiral products is of potential interest for industrial …