Biocatalysis making waves in organic chemistry

U Hanefeld, F Hollmann, CE Paul - Chemical Society Reviews, 2022 - pubs.rsc.org
Biocatalysis has an enormous impact on chemical synthesis. The waves in which
biocatalysis has developed, and in doing so changed our perception of what organic …

Enzymatic asymmetric synthesis of chiral amino acids

YP Xue, CH Cao, YG Zheng - Chemical Society Reviews, 2018 - pubs.rsc.org
Chiral amino acids are extensively applied in the pharmaceutical, food, cosmetic,
agricultural, and feedstuff industries. The development of synthetic methodologies for …

Beyond 20 in the 21st century: prospects and challenges of non-canonical amino acids in peptide drug discovery

JL Hickey, D Sindhikara, SL Zultanski… - ACS Medicinal …, 2023 - ACS Publications
Life is constructed primarily using a toolbox of 20 canonical amino acids─ relying upon
these building blocks for the assembly of proteins and peptides that regulate nearly every …

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 …

C− C bond-forming lyases in organic synthesis

M Brovetto, D Gamenara, P Saenz Mendez… - Chemical …, 2011 - ACS Publications
Lyases are enzymes that catalyze the bond construction and breaking by means other than
hydrolysis or redox reactions. Such enzymes are particular in the sense that they only …

Recent progress in stereoselective synthesis with aldolases

P Clapés, WD Fessner, GA Sprenger… - Current Opinion in …, 2010 - Elsevier
Aldol reactions constitute a powerful methodology for carbon–carbon bond formation in
synthetic organic chemistry. Biocatalysis by means of aldolases offers a unique …

Biocatalytic Methods for C C Bond Formation

K Fesko, M Gruber‐Khadjawi - ChemCatChem, 2013 - Wiley Online Library
Carbon‐carbon bond formation is among the most challenging transformations in the
organic synthetic chemistry. Enzymes capable to perform this reaction are of great interest …

Efficient asymmetric biomimetic aldol reaction of glycinates and trifluoromethyl ketones by carbonyl catalysis

A Cheng, L Zhang, Q Zhou, T Liu, J Cao… - Angewandte Chemie …, 2021 - Wiley Online Library
The direct asymmetric aldol reaction of glycinates represents an intriguing and
straightforward strategy to make biologically significant chiral β‐hydroxy‐α‐amino‐acid …

Deciphering the Key Loop: Enhancing l-Threonine Transaldolase's Catalytic Potential

Z Xi, J Rao, X Zhang, Z Liu, M Zheng, L Li… - ACS …, 2024 - ACS Publications
l-Threonine transaldolase (LTTA) is an attractive biocatalyst because of its potential
diastereoselectivity in the synthesis of β-hydroxy-α-amino acids (βHAAs). However …

Threonine aldolases: perspectives in engineering and screening the enzymes with enhanced substrate and stereo specificities

K Fesko - Applied microbiology and biotechnology, 2016 - Springer
Threonine aldolases have emerged as a powerful tool for asymmetric carbon-carbon bond
formation. These enzymes catalyse the unnatural aldol condensation of different aldehydes …