197 related articles for article (PubMed ID: 35133702)
1. Ene-Reductase: A Multifaceted Biocatalyst in Organic Synthesis.
Kumar Roy T; Sreedharan R; Ghosh P; Gandhi T; Maiti D
Chemistry; 2022 Apr; 28(21):e202103949. PubMed ID: 35133702
[TBL] [Abstract][Full Text] [Related]
2. Comparative characterization of novel ene-reductases from cyanobacteria.
Fu Y; Castiglione K; Weuster-Botz D
Biotechnol Bioeng; 2013 May; 110(5):1293-301. PubMed ID: 23280373
[TBL] [Abstract][Full Text] [Related]
3. Identification of four ene reductases and their preliminary exploration in the asymmetric synthesis of (R)-dihydrocarvone and (R)-profen derivatives.
Shi Q; Jia Y; Wang H; Li S; Li H; Guo J; Dou T; Qin B; You S
Enzyme Microb Technol; 2021 Oct; 150():109880. PubMed ID: 34489033
[TBL] [Abstract][Full Text] [Related]
4. Investigation of the stereochemical course of ene reductase-catalysed reactions by deuterium labelling.
Brenna E; Fronza G; Fuganti C; Parmeggiani F
Isotopes Environ Health Stud; 2015; 51(1):24-32. PubMed ID: 25675259
[TBL] [Abstract][Full Text] [Related]
5. Systematic methodology for the development of biocatalytic hydrogen-borrowing cascades: application to the synthesis of chiral α-substituted carboxylic acids from α-substituted α,β-unsaturated aldehydes.
Knaus T; Mutti FG; Humphreys LD; Turner NJ; Scrutton NS
Org Biomol Chem; 2015 Jan; 13(1):223-33. PubMed ID: 25372591
[TBL] [Abstract][Full Text] [Related]
6. "A Study in Yellow": Investigations in the Stereoselectivity of Ene-Reductases.
Parmeggiani F; Brenna E; Colombo D; Gatti FG; Tentori F; Tessaro D
Chembiochem; 2022 Jan; 23(1):e202100445. PubMed ID: 34586700
[TBL] [Abstract][Full Text] [Related]
7. Asymmetric Ene-Reduction by F
Kang SW; Antoney J; Lupton DW; Speight R; Scott C; Jackson CJ
Chembiochem; 2023 Apr; 24(8):e202200797. PubMed ID: 36716144
[TBL] [Abstract][Full Text] [Related]
8. Photoexcited Enzymes for Asymmetric Csp
Schmidt S
Angew Chem Int Ed Engl; 2022 Dec; 61(52):e202214313. PubMed ID: 36239986
[TBL] [Abstract][Full Text] [Related]
9. Metals in Biotechnology: Cr-Driven Stereoselective Reduction of Conjugated C=C Double Bonds.
Rauch MCR; Gallou Y; Delorme L; Paul CE; Arends IWCE; Hollmann F
Chembiochem; 2020 Apr; 21(8):1112-1115. PubMed ID: 31713969
[TBL] [Abstract][Full Text] [Related]
10. Photobiocatalysis for Abiological Transformations.
Harrison W; Huang X; Zhao H
Acc Chem Res; 2022 Apr; 55(8):1087-1096. PubMed ID: 35353478
[TBL] [Abstract][Full Text] [Related]
11. Discovery, Characterisation, Engineering and Applications of Ene Reductases for Industrial Biocatalysis.
Toogood HS; Scrutton NS
ACS Catal; 2019 May; 8(4):3532-3549. PubMed ID: 31157123
[TBL] [Abstract][Full Text] [Related]
12. Old yellow enzymes: structures and structure-guided engineering for stereocomplementary bioreduction.
Shi Q; Wang H; Liu J; Li S; Guo J; Li H; Jia X; Huo H; Zheng Z; You S; Qin B
Appl Microbiol Biotechnol; 2020 Oct; 104(19):8155-8170. PubMed ID: 32830294
[TBL] [Abstract][Full Text] [Related]
13. Applications of Ene-Reductases in the Synthesis of Flavors and Fragrances.
Fan XY; Yu Y; Yao Y; Li WD; Tao FY; Wang N
J Agric Food Chem; 2024 Jul; ():. PubMed ID: 38966982
[TBL] [Abstract][Full Text] [Related]
14. Asymmetric Reductive Carbocyclization Using Engineered Ene Reductases.
Heckenbichler K; Schweiger A; Brandner LA; Binter A; Toplak M; Macheroux P; Gruber K; Breinbauer R
Angew Chem Int Ed Engl; 2018 Jun; 57(24):7240-7244. PubMed ID: 29689601
[TBL] [Abstract][Full Text] [Related]
15. Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds.
Winkler CK; Tasnádi G; Clay D; Hall M; Faber K
J Biotechnol; 2012 Dec; 162(4):381-9. PubMed ID: 22498437
[TBL] [Abstract][Full Text] [Related]
16. Cooperative asymmetric reactions combining photocatalysis and enzymatic catalysis.
Litman ZC; Wang Y; Zhao H; Hartwig JF
Nature; 2018 Aug; 560(7718):355-359. PubMed ID: 30111790
[TBL] [Abstract][Full Text] [Related]
17. Asymmetric Reduction of (R)-Carvone through a Thermostable and Organic-Solvent-Tolerant Ene-Reductase.
Tischler D; Gädke E; Eggerichs D; Gomez Baraibar A; Mügge C; Scholtissek A; Paul CE
Chembiochem; 2020 Apr; 21(8):1217-1225. PubMed ID: 31692216
[TBL] [Abstract][Full Text] [Related]
18. Functional characterization and stability improvement of a 'thermophilic-like' ene-reductase from Rhodococcus opacus 1CP.
Riedel A; Mehnert M; Paul CE; Westphal AH; van Berkel WJ; Tischler D
Front Microbiol; 2015; 6():1073. PubMed ID: 26483784
[TBL] [Abstract][Full Text] [Related]
19. Recombinant S. cerevisiae expressing Old Yellow Enzymes from non-conventional yeasts: an easy system for selective reduction of activated alkenes.
Romano D; Contente ML; Molinari F; Eberini I; Ruvutuso E; Sensi C; Amaretti A; Rossi M; Raimondi S
Microb Cell Fact; 2014 Apr; 13():60. PubMed ID: 24767246
[TBL] [Abstract][Full Text] [Related]
20. Structural investigation into the C-terminal extension of the ene-reductase from Ralstonia (Cupriavidus) metallidurans.
Opperman DJ
Proteins; 2017 Dec; 85(12):2252-2257. PubMed ID: 28833623
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
