Vicente Gotor Fernández

Associate Professor

University of Oviedo

Spain

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Vicente Gotor Fernández is an Associate Professor at Universidad de Oviedo, Spain. His research focuses on stereoselective reactions, enzymatic processes, and the application of biocatalysis in organic synthesis, as evidenced by his recent publications on topics such as γ,γ-dihalo-β-enols, enzymatic asymmetric carboligations, and chemoenzymatic synthesis. He is also exploring innovative methods combining photochemistry and enzymatic reductions, as well as the use of ionic liquids in catalytic processes.

Vicente Gotor Fernández

Research Interests

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Articles (27)

Stereoselective Access to γ,γ‐Dihalo‐β‐Enols From Alkynes Combining Visible Light and Biocatalysis

Influence of ionic liquids on enzymatic asymmetric carboligations

Merging Iron Catalysis and Enzymatic Reduction: A Deracemization Strategy of Secondary Alcohols in Iron‐Based Deep Eutectic Solvents

Combining Photocatalytic Oxidation of β‐Chlorohydrins with Carbonyl Bioreduction in a Deracemization Approach

L–Cysteine‐Catalysed Hydration of Activated Alkynes

L–Cysteine‐Catalysed Hydration of Activated Alkynes

Access to valuable 1,4- and 1,5-diketones through gold(i) catalysis in water: application to chemoenzymatic cascades

Chemoenzymatic synthesis of Tamsulosin

BioLindlar Catalyst: Ene‐Reductase‐Promoted Selective Bioreduction of Cyanoalkynes to Give (Z)‐Cyanoalkenes

Immobilised Alcohol Dehydrogenase and Ene‐Reductase Work in Concert to Reduce Cyclohex‐2‐enone in Bulk Organic Solvent

BioLindlar Catalyst: Ene‐Reductase‐Promoted Selective Bioreduction of Cyanoalkynes to Give (Z)‐Cyanoalkenes

Front Cover Picture: Merging Organolithium Chemistry and Stereoselective Biocatalysis: Transformation of Aromatic Nitriles into Chiral Alcohols (Adv. Synth. Catal. 14/2024)

Merging Organolithium Chemistry and Stereoselective Biocatalysis: Transformation of Aromatic Nitriles into Chiral Alcohols

Photocatalytic Oxidative Cleavage of Alkenes Followed by Carbonyl Stereoselective Bioreduction for the Synthesis of Enantioenriched Secondary Alcohols

β,β‐Disubstituted Alkan‐2‐ones from Propargylic Alcohols Combining a Meyer‐Schuster Rearrangement and Asymmetric Alkene Bioreduction

Chemoselective Lipase-Catalyzed Synthesis of Amido Derivatives from 5-Hydroxymethylfurfurylamine

Laccases from Pleurotus ostreatus Applied to the Oxidation of Furfuryl Alcohol for the Synthesis of Key Compounds for Polymer Industry

From Diazonium Salts to Optically Active 1‐Arylpropan‐2‐ols Through a Sequential Photobiocatalytic Approach

Expanding the Synthetic Toolbox through Metal–Enzyme Cascade Reactions

Chemoenzymatic Cascades Combining Biocatalysis and Transition Metal Catalysis for Asymmetric Synthesis

Chemoenzymatic Cascades Combining Biocatalysis and Transition Metal Catalysis for Asymmetric Synthesis

Gold and Biocatalysis for the Stereodivergent Synthesis of Nor(pseudo)ephedrine Derivatives: Cascade Design Toward Amino Alcohols, Diols, and Diamines

Development of an amine transaminase-lipase cascade for chiral amide synthesis under flow conditions

Biotransamination of Furan‐Based Aldehydes with Isopropylamine: Enzyme Screening and pH Influence

Spectrophotometric Assay for the Detection of 2,5-Diformylfuran and Its Validation through Laccase-Mediated Oxidation of 5-Hydroxymethylfurfural

Synthesis of Optically Active <i>syn</i>- and <i>anti</i>-Chlorohydrins through a Bienzymatic Reductive Cascade

Merging Gold(I) Catalysis with Amine Transaminases in Cascade Catalysis: Chemoenzymatic Transformation of Propargylic Alcohols into Enantioenriched Allylic Amines

Collaborators (5)

Raquel Soengas

Humberto Rodriguez-Solla

Vincenzo Lettera

Ivan Lavandera

Vito Capriati

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