250 related articles for article (PubMed ID: 22498437)
41. Chemoenzymatic Oxosulfonylation-Bioreduction Sequence for the Stereoselective Synthesis of β-Hydroxy Sulfones.
López-Agudo M; Ríos-Lombardía N; González-Sabín J; Lavandera I; Gotor-Fernández V
ChemSusChem; 2022 May; 15(9):e202101313. PubMed ID: 34409744
[TBL] [Abstract][Full Text] [Related]
42. Asymmetric synthesis of both antipodes of beta-hydroxy nitriles and beta-hydroxy carboxylic acids via enzymatic reduction or sequential reduction/hydrolysis.
Ankati H; Zhu D; Yang Y; Biehl ER; Hua L
J Org Chem; 2009 Feb; 74(4):1658-62. PubMed ID: 19161324
[TBL] [Abstract][Full Text] [Related]
43. Biocatalytic approaches for the synthesis of optically pure vic-halohydrins.
Xue F; Li C; Xu Q
Appl Microbiol Biotechnol; 2021 May; 105(9):3411-3421. PubMed ID: 33851239
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. 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]
46. Production of Enantiopure Chiral Epoxides with
Gyuranová D; Štadániová R; Hegyi Z; Fischer R; Rebroš M
Molecules; 2021 Mar; 26(6):. PubMed ID: 33802034
[TBL] [Abstract][Full Text] [Related]
47. 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]
48. Stereoselective Synthesis of (+)-Annuionone A and (-)-Annuionone B.
Jiang L; Liu X; Yuan P; Zhang Y; Chen X
J Nat Prod; 2017 Apr; 80(4):805-812. PubMed ID: 28338330
[TBL] [Abstract][Full Text] [Related]
49. Highly stereoselective asymmetric 6pi-azaelectrocyclization utilizing the novel 7-alkyl substituted cis-1-amino-2-indanols: formal synthesis of 20-epiuleine.
Tanaka K; Katsumura S
J Am Chem Soc; 2002 Aug; 124(33):9660-1. PubMed ID: 12175196
[TBL] [Abstract][Full Text] [Related]
50. Stereoselectivity Switch in the Reduction of α-Alkyl-β-Arylenones by Structure-Guided Designed Variants of the Ene Reductase OYE1.
Crotti M; Parmeggiani F; Ferrandi EE; Gatti FG; Sacchetti A; Riva S; Brenna E; Monti D
Front Bioeng Biotechnol; 2019; 7():89. PubMed ID: 31080798
[TBL] [Abstract][Full Text] [Related]
51. Reinvigorating the Chiral Pool: Chemoenzymatic Approaches to Complex Peptides and Terpenoids.
Stout CN; Renata H
Acc Chem Res; 2021 Mar; 54(5):1143-1156. PubMed ID: 33543931
[TBL] [Abstract][Full Text] [Related]
52. Characteristics and biotechnology applications of aliphatic amino acid hydroxylases belonging to the Fe(II)/α-ketoglutarate-dependent dioxygenase superfamily.
Hibi M; Ogawa J
Appl Microbiol Biotechnol; 2014 May; 98(9):3869-76. PubMed ID: 24682483
[TBL] [Abstract][Full Text] [Related]
53. Metagenomic ene-reductases for the bioreduction of sterically challenging enones.
Dobrijevic D; Benhamou L; Aliev AE; Méndez-Sánchez D; Dawson N; Baud D; Tappertzhofen N; Moody TS; Orengo CA; Hailes HC; Ward JM
RSC Adv; 2019 Nov; 9(63):36608-36614. PubMed ID: 35539044
[TBL] [Abstract][Full Text] [Related]
54. "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]
55. Biocatalytic methods for the synthesis of enantioenriched odor active compounds.
Brenna E; Fuganti C; Gatti FG; Serra S
Chem Rev; 2011 Jul; 111(7):4036-72. PubMed ID: 21598986
[No Abstract] [Full Text] [Related]
56. Photoenzymatic enantioselective intermolecular radical hydroalkylation.
Huang X; Wang B; Wang Y; Jiang G; Feng J; Zhao H
Nature; 2020 Aug; 584(7819):69-74. PubMed ID: 32512577
[TBL] [Abstract][Full Text] [Related]
57. Identification of a novel ene reductase from
Zhang B; Sun J; Zheng Y; Mao X; Lin J; Wei D
RSC Adv; 2022 May; 12(22):13924-13931. PubMed ID: 35558851
[TBL] [Abstract][Full Text] [Related]
58. Applications of protein engineering to members of the old yellow enzyme family.
Amato ED; Stewart JD
Biotechnol Adv; 2015; 33(5):624-31. PubMed ID: 25940546
[TBL] [Abstract][Full Text] [Related]
59. Thermal, electrochemical and photochemical reactions involving catalytically versatile ene reductase enzymes.
Toogood HS; Scrutton NS
Enzymes; 2020; 47():491-515. PubMed ID: 32951833
[TBL] [Abstract][Full Text] [Related]
60. Metal-free intramolecular carbocyanation of alkenes: catalytic stereoselective construction of pyrrolo[2,1-a]isoquinolines with multiple substituents.
Chen J; Xu Q; Liao W
Chemistry; 2014 Oct; 20(43):13876-80. PubMed ID: 25187506
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]