Detalhe da pesquisa
1.
Expanding the Synthetic Toolbox through Metal-Enzyme Cascade Reactions.
Chem Rev
; 123(9): 5297-5346, 2023 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36626572
2.
Biotransamination of Furan-Based Aldehydes with Isopropylamine: Enzyme Screening and pH Influence.
Chembiochem
; 24(23): e202300514, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37737725
3.
A Multiplex Assay to Assess the Transaminase Activity toward Chemically Diverse Amine Donors.
Chembiochem
; 24(2): e202200614, 2023 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36385460
4.
Spectrophotometric Assay for the Detection of 2,5-Diformylfuran and Its Validation through Laccase-Mediated Oxidation of 5-Hydroxymethylfurfural.
Int J Mol Sci
; 24(23)2023 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38069183
5.
Chemoenzymatic Cascades Combining Biocatalysis and Transition Metal Catalysis for Asymmetric Synthesis.
Angew Chem Int Ed Engl
; 62(18): e202217713, 2023 04 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36744518
6.
Combination of gold and redox enzyme catalysis to access valuable enantioenriched aliphatic ß-chlorohydrins.
Org Biomol Chem
; 20(48): 9650-9658, 2022 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36413183
7.
Alcohol Dehydrogenases and N-Heterocyclic Carbene Gold(I) Catalysts: Design of a Chemoenzymatic Cascade towards Optically Active ß,ß-Disubstituted Allylic Alcohols.
Angew Chem Int Ed Engl
; 60(25): 13945-13951, 2021 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33721361
8.
Sequential Two-Step Stereoselective Amination of Allylic Alcohols through the Combination of Laccases and Amine Transaminases.
Chembiochem
; 21(1-2): 200-211, 2020 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31513330
9.
Stereoselective Bioreduction of α-diazo-ß-keto Esters.
Molecules
; 25(4)2020 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32093093
10.
Temperature-Controlled Stereodivergent Synthesis of 2,2'-Biflavanones Promoted by Samarium Diiodide.
Chemistry
; 25(57): 13104-13108, 2019 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31361369
11.
Novel chemoenzymatic oxidation of amines into oximes based on hydrolase-catalysed peracid formation.
Org Biomol Chem
; 15(15): 3196-3201, 2017 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28362446
12.
Determination of volatile compounds in cider apple juices using a covalently bonded ionic liquid coating as the stationary phase in gas chromatography.
Anal Bioanal Chem
; 409(11): 3033-3041, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28251289
13.
Stereoselective Access to 1-[2-Bromo(het)aryloxy]propan-2-amines Using Transaminases and Lipases; Development of a Chemoenzymatic Strategy Toward a Levofloxacin Precursor.
J Org Chem
; 81(20): 9765-9774, 2016 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-27662230
14.
Recent Advances in Biocatalytic Promiscuity: Hydrolase-Catalyzed Reactions for Nonconventional Transformations.
Chem Rec
; 15(4): 743-59, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26147872
15.
Chemoenzymatic asymmetric synthesis of 1,4-benzoxazine derivatives: application in the synthesis of a levofloxacin precursor.
J Org Chem
; 80(8): 3815-24, 2015 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-25786159
16.
Chiral triazolium salts and ionic liquids: from the molecular design vectors to their physical properties through specific supramolecular interactions.
Chemistry
; 19(3): 892-904, 2013 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23197418
17.
C-C Bond formation catalyzed by natural gelatin and collagen proteins.
Beilstein J Org Chem
; 9: 1111-8, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23843902
18.
Chemoselective Lipase-Catalyzed Synthesis of Amido Derivatives from 5-Hydroxymethylfurfurylamine.
ACS Sustain Chem Eng
; 11(28): 10284-10292, 2023 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37476422
19.
Laccases from Pleurotus ostreatus Applied to the Oxidation of Furfuryl Alcohol for the Synthesis of Key Compounds for Polymer Industry.
ChemSusChem
; 16(13): e202300226, 2023 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36929693
20.
Asymmetric chemoenzymatic synthesis of ramatroban using lipases and oxidoreductases.
J Org Chem
; 77(10): 4842-8, 2012 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22515546