250 related articles for article (PubMed ID: 22498437)
21. 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]
22. Characterization of an ene-reductase from Meyerozyma guilliermondii for asymmetric bioreduction of α,β-unsaturated compounds.
Zhang B; Zheng L; Lin J; Wei D
Biotechnol Lett; 2016 Sep; 38(9):1527-34. PubMed ID: 27193896
[TBL] [Abstract][Full Text] [Related]
23. Organocatalytic asymmetric vinylogous addition to quinones - formation of optically active alpha-aryl ketones.
Alemán J; Jacobsen CB; Frisch K; Overgaard J; Jørgensen KA
Chem Commun (Camb); 2008 Feb; (5):632-4. PubMed ID: 18209813
[TBL] [Abstract][Full Text] [Related]
24. Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans.
Richter N; Gröger H; Hummel W
Appl Microbiol Biotechnol; 2011 Jan; 89(1):79-89. PubMed ID: 20717668
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Structural and functional characterization of a new thermophilic-like OYE from Aspergillus flavus.
Li N; Wang Y; Meng Y; Lv Y; Zhang S; Wei S; Ma P; Hu Y; Lin H
Appl Microbiol Biotechnol; 2024 Dec; 108(1):134. PubMed ID: 38229304
[TBL] [Abstract][Full Text] [Related]
27. 'New uses for an Old Enzyme'--the Old Yellow Enzyme family of flavoenzymes.
Williams RE; Bruce NC
Microbiology (Reading); 2002 Jun; 148(Pt 6):1607-1614. PubMed ID: 12055282
[No Abstract] [Full Text] [Related]
28. Substrate scope and synthetic applications of the enantioselective reduction of α-alkyl-β-arylenones mediated by Old Yellow Enzymes.
Brenna E; Cosi SL; Ferrandi EE; Gatti FG; Monti D; Parmeggiani F; Sacchetti A
Org Biomol Chem; 2013 May; 11(18):2988-96. PubMed ID: 23532545
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. A novel catalytic and highly enantioselective approach for the synthesis of optically active carbohydrate derivatives.
Audrain H; Thorhauge J; Hazell RG; Jørgensen KA
J Org Chem; 2000 Jul; 65(15):4487-97. PubMed ID: 10959849
[TBL] [Abstract][Full Text] [Related]
31. Asymmetric tandem Michael addition-ylide olefination reaction for the synthesis of optically active cyclohexa-1,3-diene derivatives.
Ye LW; Wang SB; Wang QG; Sun XL; Tang Y; Zhou YG
Chem Commun (Camb); 2009 Jun; (21):3092-4. PubMed ID: 19462097
[TBL] [Abstract][Full Text] [Related]
32. Highly enantioselective reduction of α-methylated nitroalkenes.
Burda E; Reß T; Winkler T; Giese C; Kostrov X; Huber T; Hummel W; Gröger H
Angew Chem Int Ed Engl; 2013 Aug; 52(35):9323-6. PubMed ID: 23893708
[No Abstract] [Full Text] [Related]
33. Characterization of two styrene monooxygenases from marine microbes.
Pu W; Cui C; Guo C; Wu ZL
Enzyme Microb Technol; 2018 May; 112():29-34. PubMed ID: 29499777
[TBL] [Abstract][Full Text] [Related]
34. Preparative scale application of Mucor circinelloides ene-reductase and alcohol dehydrogenase activity for the asymmetric bioreduction of α,β-unsaturated γ-ketophosphonates.
Janicki I; Kiełbasiński P; Szeląg J; Głębski A; Szczęsna-Antczak M
Bioorg Chem; 2020 Mar; 96():103548. PubMed ID: 31982820
[TBL] [Abstract][Full Text] [Related]
35. Engineering Rieske Non-Heme Iron Oxygenases for the Asymmetric Dihydroxylation of Alkenes.
Gally C; Nestl BM; Hauer B
Angew Chem Int Ed Engl; 2015 Oct; 54(44):12952-6. PubMed ID: 26351244
[TBL] [Abstract][Full Text] [Related]
36. Solid-phase selenium-catalyzed selective allylic chlorination of polyprenoids: facile syntheses of biologically active terpenoids.
Barrero AF; Quílez Del Moral JF; Herrador MM; Cortés M; Arteaga P; Catalan JV; Sanchez EM; Arteaga JF
J Org Chem; 2006 Jul; 71(15):5811-4. PubMed ID: 16839173
[TBL] [Abstract][Full Text] [Related]
37. Old yellow enzyme: stepwise reduction of nitro-olefins and catalysis of aci-nitro tautomerization.
Meah Y; Massey V
Proc Natl Acad Sci U S A; 2000 Sep; 97(20):10733-8. PubMed ID: 10995477
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Green synthesis of enantiopure (S)-1-(benzofuran-2-yl)ethanol by whole-cell biocatalyst.
Şahin E
Chirality; 2019 Oct; 31(10):892-897. PubMed ID: 31423658
[TBL] [Abstract][Full Text] [Related]
40. Design and application of a bi-functional redox biocatalyst through covalent co-immobilization of ene-reductase and glucose dehydrogenase.
Nagy F; Gyujto I; Tasnádi G; Barna B; Balogh-Weiser D; Faber K; Poppe L; Hall M
J Biotechnol; 2020 Nov; 323():246-253. PubMed ID: 32891641
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
