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Approaching boiling point stability of an alcohol dehydrogenase through computationally-guided enzyme engineering

eLife, 2020-03, Vol.9

2020

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Structure- and computational-aided engineering of an oxidase to produce isoeugenol from a lignin-derived compound

Nature communications, 2022-11, Vol.13 (1), p.7195-7195, Article 7195

2022

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Computational Design of Enantiocomplementary Epoxide Hydrolases for Asymmetric Synthesis of Aliphatic and Aromatic Diols

Chembiochem : a European journal of chemical biology, 2020-07, Vol.21 (13), p.1893-1904

2020

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Mining the Genome of Streptomyces leeuwenhoekii : Two New Type I Baeyer-Villiger Monooxygenases From Atacama Desert

Frontiers in microbiology, 2018-07, Vol.9, p.1609-1609

2018

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An aldol approach to the enantioselective synthesis of (-)-oseltamivir phosphate

Organic & biomolecular chemistry, 2011-10, Vol.9 (20), p.6927-6929

2011

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Chemoenzymatic Synthesis of an Unnatural Deazaflavin Cofactor That Can Fuel F 420 -Dependent Enzymes

ACS catalysis, 2019-07, Vol.9 (7), p.6435-6443

2019

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Production of Hydroxy Acids: Selective Double Oxidation of Diols by Flavoprotein Alcohol Oxidase

Angewandte Chemie (International ed.), 2020-03, Vol.59 (12), p.4869-4872

International ed. in English, 2020

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Chemoenzymatic Synthesis of an Unnatural Deazaflavin Cofactor That Can Fuel F420-Dependent Enzymes

ACS catalysis, 2019-07, Vol.9 (7), p.6435-6443

2019

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The Biocatalytic Synthesis of Syringaresinol from 2,6-Dimethoxy-4-allylphenol in One-Pot Using a Tailored Oxidase/Peroxidase System

ACS catalysis, 2018-06, Vol.8 (6), p.5549-5552

2018

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Enantio- and regioselective ene-reductions using F420H2-dependent enzymes

Chemical communications (Cambridge, England), 2018-10, Vol.54 (79), p.11208-11211

2018

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Facile Stereoselective Reduction of Prochiral Ketones by using an F 420 -dependent Alcohol Dehydrogenase

Chembiochem : a European journal of chemical biology, 2021-01, Vol.22 (1), p.156-159

2021

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Facile Stereoselective Reduction of Prochiral Ketones by using an F420‐dependent Alcohol Dehydrogenase

Chembiochem : a European journal of chemical biology, 2021-01, Vol.22 (1), p.156-159

2021

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One-Pot Biocatalytic Synthesis of rac-Syringaresinol from a Lignin-Derived Phenol

ACS catalysis, 2023-11, Vol.13 (22), p.14639-14649

2023

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Chemoenzymatic Synthesis of the Most Pleasant Stereoisomer of Jessemal

Journal of organic chemistry, 2022-05, Vol.87 (9), p.6499-6503

2022

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Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers

ACS catalysis, 2020-11, Vol.10 (21), p.13050-13057

2020

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Discovery, Biocatalytic Exploration and Structural Analysis of a 4‐Ethylphenol Oxidase from Gulosibacter chungangensis

Chembiochem : a European journal of chemical biology, 2021-11, Vol.22 (22), p.3225-3233

2021

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Substrate binding tunes the reactivity of hispidin 3-hydroxylase, a flavoprotein monooxygenase involved in fungal bioluminescence

The Journal of biological chemistry, 2020-11, Vol.295 (47), p.16013-16022

2020

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Enantioselective Synthesis of the Platensimycin Core by Silver(I)-Promoted Cyclization of Δ 6 -α-Iodoketone

Chemistry : a European journal, 2019-03, Vol.25 (17), p.4340-4344

2019

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Enantioselective Synthesis of the Platensimycin Core by Silver(I)‐Promoted Cyclization of Δ6‐α‐Iodoketone

Chemistry : a European journal, 2019-03, Vol.25 (17), p.4340-4344

2019

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Total Synthesis of ( + )-Swainsonine, (–)- Swainsonine, ( + )-8- epi -Swainsonine and ( + )- Dideoxy-Imino-Lyxitol by an Organocatalyzed Aldolization/Reductive Amination Sequence

Natural product communications, 2022-04, Vol.17 (4), p.1934578

2022

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Enantio- and regioselective ene-reductions using F420H2-dependent enzymesElectronic supplementary information (ESI) available: Experimental procedures, Fig. S1 and S2, Tables S1 and S2, synthesis of substrates and products, chiral GC chromatograms, and NMR spectra (PDF). See DOI: 10.1039/c8cc04449j

2018-10

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Enantio- and regioselective ene-reductions using F 420 H 2 -dependent enzymes

Chemical communications (Cambridge, England), 2018-10, Vol.54 (79), p.11208-11211

2018

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Introducing an Artificial Deazaflavin Cofactor in Escherichia coli and Saccharomyces cerevisiae

ACS synthetic biology, 2022-02, Vol.11 (2), p.938-952

2022

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A convenient procedure for the preparation of Garner’s aldehyde

Tetrahedron: asymmetry, 2012-04, Vol.23 (8), p.602-604

2012

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A Biocatalytic One‐Pot Approach for the Preparation of Lignin Oligomers Using an Oxidase/Peroxidase Cascade Enzyme System

Advanced synthesis & catalysis, 2017-10, Vol.359 (19), p.3354-3361

2017

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Approaching boiling point stability of an alcohol dehydrogenase through computationally-guided enzyme engineering

Structure- and computational-aided engineering of an oxidase to produce isoeugenol from a lignin-derived compound

Computational Design of Enantiocomplementary Epoxide Hydrolases for Asymmetric Synthesis of Aliphatic and Aromatic Diols

Mining the Genome of Streptomyces leeuwenhoekii : Two New Type I Baeyer-Villiger Monooxygenases From Atacama Desert

An aldol approach to the enantioselective synthesis of (-)-oseltamivir phosphate

Chemoenzymatic Synthesis of an Unnatural Deazaflavin Cofactor That Can Fuel F 420 -Dependent Enzymes

Production of Hydroxy Acids: Selective Double Oxidation of Diols by Flavoprotein Alcohol Oxidase

Chemoenzymatic Synthesis of an Unnatural Deazaflavin Cofactor That Can Fuel F420-Dependent Enzymes

The Biocatalytic Synthesis of Syringaresinol from 2,6-Dimethoxy-4-allylphenol in One-Pot Using a Tailored Oxidase/Peroxidase System

Enantio- and regioselective ene-reductions using F420H2-dependent enzymes

Facile Stereoselective Reduction of Prochiral Ketones by using an F 420 -dependent Alcohol Dehydrogenase

Facile Stereoselective Reduction of Prochiral Ketones by using an F420‐dependent Alcohol Dehydrogenase

One-Pot Biocatalytic Synthesis of rac-Syringaresinol from a Lignin-Derived Phenol

Chemoenzymatic Synthesis of the Most Pleasant Stereoisomer of Jessemal

Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers

Discovery, Biocatalytic Exploration and Structural Analysis of a 4‐Ethylphenol Oxidase from Gulosibacter chungangensis

Substrate binding tunes the reactivity of hispidin 3-hydroxylase, a flavoprotein monooxygenase involved in fungal bioluminescence

Enantioselective Synthesis of the Platensimycin Core by Silver(I)-Promoted Cyclization of Δ 6 -α-Iodoketone

Enantioselective Synthesis of the Platensimycin Core by Silver(I)‐Promoted Cyclization of Δ6‐α‐Iodoketone

Total Synthesis of ( + )-Swainsonine, (–)- Swainsonine, ( + )-8- epi -Swainsonine and ( + )- Dideoxy-Imino-Lyxitol by an Organocatalyzed Aldolization/Reductive Amination Sequence

Enantio- and regioselective ene-reductions using F420H2-dependent enzymesElectronic supplementary information (ESI) available: Experimental procedures, Fig. S1 and S2, Tables S1 and S2, synthesis of substrates and products, chiral GC chromatograms, and NMR spectra (PDF). See DOI: 10.1039/c8cc04449j

Enantio- and regioselective ene-reductions using F 420 H 2 -dependent enzymes

Introducing an Artificial Deazaflavin Cofactor in Escherichia coli and Saccharomyces cerevisiae

A convenient procedure for the preparation of Garner’s aldehyde

A Biocatalytic One‐Pot Approach for the Preparation of Lignin Oligomers Using an Oxidase/Peroxidase Cascade Enzyme System

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