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Synthesis and cytotoxic evaluation of monocarbonyl curcuminoids and their pyrazoline derivatives

Monatshefte für Chemie, 2019-12, Vol.150 (12), p.2045-2051

2019

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Diastereoselective Synthesis of Bicyclic γ-Lactams via Ring Expansion of Monocyclic β-Lactams

Journal of organic chemistry, 2009-02, Vol.74 (4), p.1644-1649

2009

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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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Synthesis and reactivity of 4-(trifluoromethyl)azetidin-2-ones

Monatshefte für Chemie, 2018-04, Vol.149 (4), p.687-700

2018

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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 and cancer cell cytotoxicity of 2-aryl-4-(4-aryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes

Phytochemistry letters, 2023-06, Vol.55, p.117-123

2023

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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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Identification of mercaptoacetamide-based HDAC6 inhibitors via a lean inhibitor strategy: screening, synthesis, and biological evaluation

Chemical communications (Cambridge, England), 2022-05, Vol.58 (42), p.6239-6242

2022

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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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Covalent organic framework supported palladium catalysts

Journal of materials chemistry. A, Materials for energy and sustainability, 2022-10, Vol.1 (39), p.277-2729

2022

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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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Chemoenzymatic Approach toward the Synthesis of 3‑O‑(α/β)-Glucosylated 3‑Hydroxy-β-lactams

ACS omega, 2018-11, Vol.3 (11), p.15235-15245

2018

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Engineering the specificity of trehalose phosphorylase as a general strategy for the production of glycosyl phosphates

Chemical communications (Cambridge, England), 2014-07, Vol.50 (58), p.7834-7836

2014

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Microwave-Assisted Synthesis of Isopropyl β-(3,4-Dihydroxyphenyl)-α-hydroxypropanoate

Journal of chemistry, 2013-01, Vol.2013, p.1-7

2013

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LiAlH4-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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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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Synthesis of 1,4‐Thiazepane‐Based Curcuminoids with Promising Anticancer Activity

Chemistry : a European journal, 2019-09, Vol.25 (54), p.12583-12600

2019

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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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Rapid Reduction of Alkenes and Alkynes over Pd Nanoparticles Supported on Sulfonated Porous Carbon

Journal of chemistry, 2013-01, Vol.2013, p.1-7

2013

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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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Synthesis and cytotoxic evaluation of monocarbonyl curcuminoids and their pyrazoline derivatives

Diastereoselective Synthesis of Bicyclic γ-Lactams via Ring Expansion of Monocyclic β-Lactams

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

Synthesis and reactivity of 4-(trifluoromethyl)azetidin-2-ones

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

Synthesis and cancer cell cytotoxicity of 2-aryl-4-(4-aryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes

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

Identification of mercaptoacetamide-based HDAC6 inhibitors via a lean inhibitor strategy: screening, synthesis, and biological evaluation

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

Covalent organic framework supported palladium catalysts

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

Chemoenzymatic Approach toward the Synthesis of 3‑O‑(α/β)-Glucosylated 3‑Hydroxy-β-lactams

Engineering the specificity of trehalose phosphorylase as a general strategy for the production of glycosyl phosphates

Microwave-Assisted Synthesis of Isopropyl β-(3,4-Dihydroxyphenyl)-α-hydroxypropanoate

LiAlH4-Induced Selective Ring Rearrangement of 2-(2-Cyanoethyl)aziridines toward 2-(Aminomethyl)pyrrolidines and 3-Aminopiperidines as Eligible Heterocyclic Building Blocks

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

Synthesis of 1,4‐Thiazepane‐Based Curcuminoids with Promising Anticancer Activity

Rapid Reduction of Alkenes and Alkynes over Pd Nanoparticles Supported on Sulfonated Porous Carbon

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

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