Ene‐reductase: a multifaceted biocatalyst in organic synthesis
T Kumar Roy, R Sreedharan, P Ghosh… - … A European Journal, 2022 - Wiley Online Library
Biocatalysis integrate microbiologists, enzymologists, and organic chemists to access the
repertoire of pharmaceutical and agrochemicals with high chemoselectivity, regioselectivity …
repertoire of pharmaceutical and agrochemicals with high chemoselectivity, regioselectivity …
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 …
synthetic organic chemistry, a broad variety of biocatalysts are being applied in an …
Discovery, characterization, engineering, and applications of ene-reductases for industrial biocatalysis
Recent studies of multiple enzyme families collectively called ene-reductases (ERs) have
highlighted potential industrial applications of these biocatalysts in the production of fine and …
highlighted potential industrial applications of these biocatalysts in the production of fine and …
Ancestral sequence reconstruction enhances gene mining efforts for industrial ene reductases by expanding enzyme panels with thermostable catalysts
J Livada, AM Vargas, CA Martinez, RD Lewis - ACS Catalysis, 2023 - ACS Publications
Ancestral sequence reconstruction (ASR) has been used to produce enzymes that exhibit
enhanced stability, activity, and promiscuity compared to wild-type (WT) enzymes. In this …
enhanced stability, activity, and promiscuity compared to wild-type (WT) enzymes. In this …
Asymmetric α-benzylation of cyclic ketones enabled by concurrent chemical aldol condensation and biocatalytic reduction
Y Liu, T Ma, Z Guo, L Zhou, G Liu, Y He, L Ma… - Nature …, 2024 - nature.com
Chemoenzymatic cascade catalysis has emerged as a revolutionary tool for streamlining
traditional retrosynthetic disconnections, creating new possibilities for the asymmetric …
traditional retrosynthetic disconnections, creating new possibilities for the asymmetric …
Biocatalytic reduction of activated CC-bonds and beyond: emerging trends
Highlights•OYE homologues (ene-reductases) are widely used for C double bond C-bond
reduction reactions.•Protein diversity screening and protein engineering aim at providing …
reduction reactions.•Protein diversity screening and protein engineering aim at providing …
“A study in yellow”: Investigations in the stereoselectivity of ene‐reductases
Ene‐reductases from the Old Yellow Enzyme (OYE) superfamily are a well‐known and
efficient biocatalytic alternative for the asymmetric reduction of C= C bonds. Considering the …
efficient biocatalytic alternative for the asymmetric reduction of C= C bonds. Considering the …
Catalytic asymmetric conjugate reduction
G Lonardi, R Parolin, G Licini… - Angewandte Chemie …, 2023 - Wiley Online Library
Enantioselective reduction reactions are privileged transformations for the construction of
trisubstituted stereogenic centers. While these include established synthetic strategies, such …
trisubstituted stereogenic centers. While these include established synthetic strategies, such …
Asymmetric reductive carbocyclization using engineered ene reductases
K Heckenbichler, A Schweiger… - Angewandte Chemie …, 2018 - Wiley Online Library
Ene reductases from the Old Yellow Enzyme (OYE) family reduce the C= C double bond in
α, β‐unsaturated compounds bearing an electron‐withdrawing group, for example, a …
α, β‐unsaturated compounds bearing an electron‐withdrawing group, for example, a …
Visible-light-driven palladium-catalyzed Dowd–Beckwith ring expansion/C–C bond formation cascade
L Chen, LN Guo, S Liu, L Liu, XH Duan - Chemical Science, 2021 - pubs.rsc.org
A visible-light-induced palladium-catalyzed Dowd–Beckwith ring expansion/C–C bond
formation cascade is described. A range of six to nine-membered β-alkenylated cyclic …
formation cascade is described. A range of six to nine-membered β-alkenylated cyclic …