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Synthesis and applications of benzohydroxamic acid-based histone deacetylase inhibitors

European journal of medicinal chemistry, 2017-07, Vol.135, p.174-195

2017

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The Zinc-Binding Group Effect: Lessons from Non-Hydroxamic Acid Vorinostat Analogs

Journal of medicinal chemistry, 2023-06, Vol.66 (12), p.7698-7729

2023

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High-yield synthesis of 2-O-α-d-glucosyl-d-glycerate by a bifunctional glycoside phosphorylase

Applied microbiology and biotechnology, 2024-12, Vol.108 (1), p.55-55, Article 55

2024

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Exploring the sequence diversity in glycoside hydrolase family 13_18 reveals a novel glucosylglycerol phosphorylase

Applied microbiology and biotechnology, 2018-04, Vol.102 (7), p.3183-3191

2018

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Recent contributions of quinolines to antimalarial and anticancer drug discovery research

European journal of medicinal chemistry, 2021-12, Vol.226, p.113865-113865, Article 113865

2021

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Synthesis and biological evaluation of novel quinoline-piperidine scaffolds as antiplasmodium agents

European journal of medicinal chemistry, 2020-07, Vol.198, p.112330, Article 112330

2020

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Design and synthesis of novel ferrocene-quinoline conjugates and evaluation of their electrochemical and antiplasmodium properties

European journal of medicinal chemistry, 2020-02, Vol.187, p.111963-111963, Article 111963

2020

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Engineering Comamonas testosteroni for the production of 2-pyrone-4,6-dicarboxylic acid as a promising building block

Microbial cell factories, 2023-09, Vol.22 (1), p.1-188, Article 188

2023

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Carbonylation of Aziridines as a Powerful Tool for the Synthesis of Functionalized [beta]-Lactams

European journal of organic chemistry, 2017-11, Vol.2017 (40), p.5943

2017

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Carboxylic Acid Bioisosteres in Medicinal Chemistry: Synthesis and Properties

Journal of chemistry, 2022, Vol.2022, p.1-21

2022

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Antibacterial and β‐Lactamase Inhibitory Activity of Monocyclic β‐Lactams

Medicinal research reviews, 2018-03, Vol.38 (2), p.426-503

2018

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Synthesis of novel curcuminoids accommodating a central β-enaminone motif and their impact on cell growth and oxidative stress

European journal of medicinal chemistry, 2016-11, Vol.123, p.727-736

2016

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An update on the synthesis and reactivity of spiro-fused Î²-lactams

ARKIVOC free online journal of organic chemistry, 2019-03, Vol.2018 (6), p.314-347

2019

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Design, Synthesis, and Antiviral Evaluation of Purine-β-lactam and Purine-aminopropanol Hybrids

Journal of medicinal chemistry, 2012-06, Vol.55 (11), p.5637-5641

2012

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LiAlH 4 ‐Induced Thia‐Aza‐Payne Rearrangement of Functionalized 2‐(Thiocyanatomethyl)aziridines into 2‐(Aminomethyl)thiiranes as an Entry to 5‐(Chloromethyl)thiazolidin‐2‐ones

European journal of organic chemistry, 2017-06, Vol.2017 (22), p.3229-3233

2017

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Converting bulk sugars into prebiotics: semi-rational design of a transglucosylase with controlled selectivity

Chemical communications (Cambridge, England), 2016-03, Vol.52 (18), p.3687-3689

2016

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Selective pharmacological inhibitors of HDAC6 reveal biochemical activity but functional tolerance in cancer models

International journal of cancer, 2019-08, Vol.145 (3), p.735-747

2019

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Synthesis of Novel 2-Alkoxy-3-amino-3-arylpropan-1-ols and 5-Alkoxy-4-aryl-1,3-oxazinanes with Antimalarial Activity

Journal of medicinal chemistry, 2009-07, Vol.52 (13), p.4058-4062

2009

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Cobalt carbonyl-catalyzed carbonylation of functionalized aziridines to versatile β-lactam building blocksElectronic supplementary information (ESI) available: Experimental procedures, characterization data, 1H NMR and 13C NMR spectra. CCDC 1529989-1529991. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ob00832e

2017-06

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Biocatalytic production of novel glycolipids with cellodextrin phosphorylase

Bioresource technology, 2012-07, Vol.115, p.84-87

2012

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Synthesis of 2-(aminomethyl)aziridines and their microwave-assisted ring opening to 1,2,3-triaminopropanes as novel antimalarial pharmacophores

European journal of medicinal chemistry, 2011-02, Vol.46 (2), p.579-587

2011

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LiAlH 4 ‐Induced Selective Ring Rearrangement of 2‐(2‐Cyanoethyl)aziridines toward 2‐(Aminomethyl)pyrrolidines and 3‐Aminopiperidines as Eligible Heterocyclic Building Blocks

Chemistry : a European journal, 2016-03, Vol.22 (14), p.4945-4951

2016

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LiAlH sub(4)-Induced Selective Ring Rearrangement of 2-(2-Cyanoethyl)aziridines toward 2-(Aminomethyl)pyrrolidines and 3-Aminopiperidines as Eligible Heterocyclic Building Blocks

Chemistry : a European journal, 2016-03, Vol.22 (14), p.4945-4951

2016

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Theoretical insight into the regioselective ring-expansions of bicyclic aziridinium ionsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ob02253k

2018-01

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Synthesis of functionalized 3-, 5-, 6- and 8-aminoquinolines via intermediate (3-pyrrolin-1-yl)- and (2-oxopyrrolidin-1-yl)quinolines and evaluation of their antiplasmodial and antifungal activity

European journal of medicinal chemistry, 2015-03, Vol.92, p.91-102

2015

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1 – 25 von 159

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Synthesis and applications of benzohydroxamic acid-based histone deacetylase inhibitors

The Zinc-Binding Group Effect: Lessons from Non-Hydroxamic Acid Vorinostat Analogs

High-yield synthesis of 2-O-α-d-glucosyl-d-glycerate by a bifunctional glycoside phosphorylase

Exploring the sequence diversity in glycoside hydrolase family 13_18 reveals a novel glucosylglycerol phosphorylase

Recent contributions of quinolines to antimalarial and anticancer drug discovery research

Synthesis and biological evaluation of novel quinoline-piperidine scaffolds as antiplasmodium agents

Design and synthesis of novel ferrocene-quinoline conjugates and evaluation of their electrochemical and antiplasmodium properties

Engineering Comamonas testosteroni for the production of 2-pyrone-4,6-dicarboxylic acid as a promising building block

Carbonylation of Aziridines as a Powerful Tool for the Synthesis of Functionalized [beta]-Lactams

Carboxylic Acid Bioisosteres in Medicinal Chemistry: Synthesis and Properties

Antibacterial and β‐Lactamase Inhibitory Activity of Monocyclic β‐Lactams

Synthesis of novel curcuminoids accommodating a central β-enaminone motif and their impact on cell growth and oxidative stress

An update on the synthesis and reactivity of spiro-fused Î²-lactams

Design, Synthesis, and Antiviral Evaluation of Purine-β-lactam and Purine-aminopropanol Hybrids

LiAlH 4 ‐Induced Thia‐Aza‐Payne Rearrangement of Functionalized 2‐(Thiocyanatomethyl)aziridines into 2‐(Aminomethyl)thiiranes as an Entry to 5‐(Chloromethyl)thiazolidin‐2‐ones

Converting bulk sugars into prebiotics: semi-rational design of a transglucosylase with controlled selectivity

Selective pharmacological inhibitors of HDAC6 reveal biochemical activity but functional tolerance in cancer models

Synthesis of Novel 2-Alkoxy-3-amino-3-arylpropan-1-ols and 5-Alkoxy-4-aryl-1,3-oxazinanes with Antimalarial Activity

Biocatalytic production of novel glycolipids with cellodextrin phosphorylase

Synthesis of 2-(aminomethyl)aziridines and their microwave-assisted ring opening to 1,2,3-triaminopropanes as novel antimalarial pharmacophores

LiAlH 4 ‐Induced Selective Ring Rearrangement of 2‐(2‐Cyanoethyl)aziridines toward 2‐(Aminomethyl)pyrrolidines and 3‐Aminopiperidines as Eligible Heterocyclic Building Blocks

LiAlH sub(4)-Induced Selective Ring Rearrangement of 2-(2-Cyanoethyl)aziridines toward 2-(Aminomethyl)pyrrolidines and 3-Aminopiperidines as Eligible Heterocyclic Building Blocks

Theoretical insight into the regioselective ring-expansions of bicyclic aziridinium ionsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ob02253k

Synthesis of functionalized 3-, 5-, 6- and 8-aminoquinolines via intermediate (3-pyrrolin-1-yl)- and (2-oxopyrrolidin-1-yl)quinolines and evaluation of their antiplasmodial and antifungal activity

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