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Bioreduction of 4′-Hydroxychalcone in Deep Eutectic Solvents: Optimization and Efficacy with Various Yeast Strains

International journal of molecular sciences, 2024-07, Vol.25 (13), p.7152

2024

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Lipase-mediated Baeyer–Villiger oxidation of benzylcyclopentanones in ester solvents and deep eutectic solvents

Scientific reports, 2022-08, Vol.12 (1), p.14795-14795, Article 14795

2022

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Microbial Transformations of Halolactones and Evaluation of Their Antiproliferative Activity

International journal of molecular sciences, 2023-04, Vol.24 (8), p.7587

2023

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Synthesis and Antimicrobial Activity of Methoxy- Substituted γ-Oxa-ε-lactones Derived from Flavanones

Molecules (Basel, Switzerland), 2019-11, Vol.24 (22), p.4151

2019

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Deciphering minimal antigenic epitopes associated with Burkholderia pseudomallei and Burkholderia mallei lipopolysaccharide O-antigens

Nature communications, 2017-07, Vol.8 (1), p.115-13, Article 115

2017

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Regio- and enantioselective microbial hydroxylation and evaluation of cytotoxic activity of β-cyclocitral-derived halolactones

PloS one, 2017-08, Vol.12 (8), p.e0183429-e0183429

2017

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Microbial Asymmetric Functionalization of β-Cyclocitral-Derived Tetramethyl-Substituted γ-Lactone

Molecules (Basel, Switzerland), 2019-02, Vol.24 (4), p.666

2019

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Microbial Hydrolysis of Racemic β-Aryl-γ-ethylidene-γ-lactones and Antifeedant Activity of the Products against Alphitobius diaperinus Panzer

Molecules (Basel, Switzerland), 2018-06, Vol.23 (7), p.1516

2018

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Microbial transformations of halolactones with p-menthane system

Journal of bioscience and bioengineering, 2015-01, Vol.119 (1), p.72-76

2015

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Preparation of Enantiomeric β-(2',5'-Dimethylphenyl)Bromolactones, Their Antiproliferative Activity and Effect on Biological Membranes

Molecules (Basel, Switzerland), 2018-11, Vol.23 (11), p.3035

2018

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Biotechnological Approach for the Production of Enantiomeric Hydroxylactones Derived from Benzaldehyde and Evaluation of Their Cytotoxic Activity

Catalysts, 2020-11, Vol.10 (11), p.1313

2020

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Chemoenzymatic Synthesis of Enantiomeric, Bicyclic δ-Halo-γ-lactones with a Cyclohexane Ring, Their Biological Activity and Interaction with Biological Membranes

Biomolecules (Basel, Switzerland), 2020-01, Vol.10 (1), p.95

2020

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Baker’s yeast-mediated asymmetric reduction of ethyl 3-oxobutanoate in deep eutectic solvents

Process biochemistry (1991), 2015-11, Vol.50 (11), p.1788-1792

2015

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Enantiomeric trans β-aryl-δ-iodo-γ-lactones derived from 2,5-dimethylbenzaldehyde induce apoptosis in canine lymphoma cell lines by downregulation of anti-apoptotic Bcl-2 family members Bcl-xL and Bcl-2

Bioorganic & medicinal chemistry letters, 2018-04, Vol.28 (7), p.1171-1177

2018

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Regio- and enantioselective microbial hydroxylation and evaluation of cytotoxic activity of [beta]-cyclocitral-derived halolactones

PloS one, 2017-08, Vol.12 (8), p.e0183429

2017

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Convenient Chemoenzymatic Route to Optically Active β-Aryl-δ-iodo-γ-lactones and β-Aryl-γ-iodo-δ-lactones with the Defined Configurations of Stereogenic Centers

European journal of organic chemistry, 2015-01, Vol.2015 (3), p.605-615

2015

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Optically active stereoisomers of 5-(1-iodoethyl)-4-(4′-isopropylphenyl)dihydrofuran-2-one: The effect of the configuration of stereocenters on apoptosis induction in canine cancer cell lines

Chemico-biological interactions, 2017-01, Vol.261, p.18-26

2017

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4′-Methoxyphenacyl-Assisted Synthesis of β‑Kdo Glycosides

Journal of organic chemistry, 2016-11, Vol.81 (22), p.10585-10599

2016

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Convenient Chemoenzymatic Route to Optically Active [beta]-Aryl-[delta]-iodo-[gamma]-lactones and [beta]-Aryl-[gamma]-iodo-[delta]-lactones with the Defined Configurations of Stereogenic Centers

European journal of organic chemistry, 2015-01, Vol.2015 (3), p.605

2015

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Synthesis and anticancer activity of novel halolactones with β-aryl substituents from simple aromatic aldehydes

Tetrahedron, 2013-12, Vol.69 (48), p.10414-10423

2013

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Lactones 46. Synthesis, antifeedant and antibacterial activity of γ -lactones with a p -methoxyphenyl substituent: Biologically active lactones with a methoxyphenyl substituent

Pest management science, 2016-03, Vol.72 (3), p.489-496

2016

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Lactones 43. New biologically active lactones: β-cyclocitral derivatives

Pest management science, 2014-02, Vol.70 (2), p.286-294

2014

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Conformational flexibility of the glycosidase NagZ allows it to bind structurally diverse inhibitors to suppress β‐lactam antibiotic resistance

Protein science, 2017-06, Vol.26 (6), p.1161-1170

2017

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Lactones 46. Synthesis, antifeedant and antibacterial activity of γ‐lactones with a p‐methoxyphenyl substituent

Pest management science, 2016-03, Vol.72 (3), p.489-496

2016

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Chiral δ-iodo-γ-lactones derived from cuminaldehyde, 2,5-dimethylbenzaldehyde and piperonal: chemoenzymatic synthesis and antiproliferative activity

Tetrahedron: asymmetry, 2016-04, Vol.27 (6), p.227-237

2016

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Bioreduction of 4′-Hydroxychalcone in Deep Eutectic Solvents: Optimization and Efficacy with Various Yeast Strains

Lipase-mediated Baeyer–Villiger oxidation of benzylcyclopentanones in ester solvents and deep eutectic solvents

Microbial Transformations of Halolactones and Evaluation of Their Antiproliferative Activity

Synthesis and Antimicrobial Activity of Methoxy- Substituted γ-Oxa-ε-lactones Derived from Flavanones

Deciphering minimal antigenic epitopes associated with Burkholderia pseudomallei and Burkholderia mallei lipopolysaccharide O-antigens

Regio- and enantioselective microbial hydroxylation and evaluation of cytotoxic activity of β-cyclocitral-derived halolactones

Microbial Asymmetric Functionalization of β-Cyclocitral-Derived Tetramethyl-Substituted γ-Lactone

Microbial Hydrolysis of Racemic β-Aryl-γ-ethylidene-γ-lactones and Antifeedant Activity of the Products against Alphitobius diaperinus Panzer

Microbial transformations of halolactones with p-menthane system

Preparation of Enantiomeric β-(2',5'-Dimethylphenyl)Bromolactones, Their Antiproliferative Activity and Effect on Biological Membranes

Biotechnological Approach for the Production of Enantiomeric Hydroxylactones Derived from Benzaldehyde and Evaluation of Their Cytotoxic Activity

Chemoenzymatic Synthesis of Enantiomeric, Bicyclic δ-Halo-γ-lactones with a Cyclohexane Ring, Their Biological Activity and Interaction with Biological Membranes

Baker’s yeast-mediated asymmetric reduction of ethyl 3-oxobutanoate in deep eutectic solvents

Enantiomeric trans β-aryl-δ-iodo-γ-lactones derived from 2,5-dimethylbenzaldehyde induce apoptosis in canine lymphoma cell lines by downregulation of anti-apoptotic Bcl-2 family members Bcl-xL and Bcl-2

Regio- and enantioselective microbial hydroxylation and evaluation of cytotoxic activity of [beta]-cyclocitral-derived halolactones

Convenient Chemoenzymatic Route to Optically Active β-Aryl-δ-iodo-γ-lactones and β-Aryl-γ-iodo-δ-lactones with the Defined Configurations of Stereogenic Centers

Optically active stereoisomers of 5-(1-iodoethyl)-4-(4′-isopropylphenyl)dihydrofuran-2-one: The effect of the configuration of stereocenters on apoptosis induction in canine cancer cell lines

4′-Methoxyphenacyl-Assisted Synthesis of β‑Kdo Glycosides

Convenient Chemoenzymatic Route to Optically Active [beta]-Aryl-[delta]-iodo-[gamma]-lactones and [beta]-Aryl-[gamma]-iodo-[delta]-lactones with the Defined Configurations of Stereogenic Centers

Synthesis and anticancer activity of novel halolactones with β-aryl substituents from simple aromatic aldehydes

Lactones 46. Synthesis, antifeedant and antibacterial activity of γ -lactones with a p -methoxyphenyl substituent: Biologically active lactones with a methoxyphenyl substituent

Lactones 43. New biologically active lactones: β-cyclocitral derivatives

Conformational flexibility of the glycosidase NagZ allows it to bind structurally diverse inhibitors to suppress β‐lactam antibiotic resistance

Lactones 46. Synthesis, antifeedant and antibacterial activity of γ‐lactones with a p‐methoxyphenyl substituent

Chiral δ-iodo-γ-lactones derived from cuminaldehyde, 2,5-dimethylbenzaldehyde and piperonal: chemoenzymatic synthesis and antiproliferative activity

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