Engineering new catalytic activities in enzymes

K Chen, FH Arnold - Nature Catalysis, 2020 - nature.com
The efficiency, selectivity and sustainability benefits offered by enzymes are enticing
chemists to consider biocatalytic transformations to complement or even supplant more …

Enantioselective chemo‐and biocatalysis: partners in retrosynthesis

M Hönig, P Sondermann, NJ Turner… - Angewandte Chemie …, 2017 - Wiley Online Library
Recent developments of stereoselective biocatalytic and chemocatalytic methods are
discussed. The review provides a guide to the use of biocatalytic methods in the area of …

Visible-light-mediated formal carbene insertion reaction: enantioselective synthesis of 1, 4-dicarbonyl compounds containing all-carbon quaternary stereocenter

H Zhang, Z Wang, Z Wang, Y Chu, S Wang… - ACS Catalysis, 2022 - ACS Publications
We developed an efficient visible-light-mediated formal carbene insertion reaction of 1, 3-
diketones with diazoesters for the construction of enantioenriched 1, 4-dicarbonyl …

Building bridges: Biocatalytic C–C-bond formation toward multifunctional products

NG Schmidt, E Eger, W Kroutil - ACS catalysis, 2016 - ACS Publications
Carbon–carbon bond formation is the key reaction for organic synthesis to construct the
carbon framework of organic molecules. The review gives a selection of biocatalytic C–C …

Structure, chemical synthesis, and biosynthesis of prodiginine natural products

DX Hu, DM Withall, GL Challis, RJ Thomson - Chemical reviews, 2016 - ACS Publications
The prodiginine family of bacterial alkaloids is a diverse set of heterocyclic natural products
that have likely been known to man since antiquity. In more recent times, these alkaloids …

Chemomimetic biocatalysis: exploiting the synthetic potential of cofactor-dependent enzymes to create new catalysts

CK Prier, FH Arnold - Journal of the American Chemical Society, 2015 - ACS Publications
Despite the astonishing breadth of enzymes in nature, no enzymes are known for many of
the valuable catalytic transformations discovered by chemists. Recent work in enzyme …

Highly enantioselective synthesis of α‐amino acid derivatives by an NHC‐catalyzed intermolecular Stetter reaction

T Jousseaume, NE Wurz, F Glorius - Angewandte Chemie International …, 2011 - infona.pl
PROTONtype: An NHC‐catalyzed (NHC= N‐heterocyclic carbene), highly asymmetric
intermolecular Stetter reaction allows the atom‐economic and efficient formation of valuable …

Catalytic asymmetric intermolecular Stetter reaction of enals with nitroalkenes: enhancement of catalytic efficiency through bifunctional additives

DA DiRocco, T Rovis - Journal of the American Chemical Society, 2011 - ACS Publications
An asymmetric intermolecular Stetter reaction of enals with nitroalkenes catalyzed by chiral
N-heterocyclic carbenes has been developed. The reaction rate and efficiency are …

Highly Asymmetric NHC‐Catalyzed Hydroacylation of Unactivated Alkenes

I Piel, M Steinmetz, K Hirano… - Angewandte Chemie …, 2011 - Wiley Online Library
N-Heterocyclic carbene (NHC)-catalyzed umpolung reactions [1] offer an elegant access to
several important classes of compounds, such as benzoins [2] or g-butyrolactones.[3] In …

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 …