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High-yield synthesis of 2-O-α-d-glucosyl-d-glycerate by a bifunctional glycoside phosphorylase
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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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- Journal Article
- A1
- open access
Synthesis of the 1,5-benzothiazepane scaffold : established methods and new developments
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- Journal Article
- A1
- open access
Synthesis of 4‐imidoyl‐, 4‐oxiranyl‐ and 4‐propargyloxyphenyl‐substituted β‐lactam building blocks
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- Journal Article
- A1
- open access
Engineering Comamonas testosteroni for the production of 2-pyrone-4,6-dicarboxylic acid as a promising building block
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- Journal Article
- A1
- open access
The zinc-binding group effect : lessons from non-hydroxamic acid vorinostat analogs
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- Journal Article
- A1
- open access
Synthesis and cancer cell cytotoxicity of 2-aryl-4-(4-aryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes
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Exposure of curcumin (analogues) to 2D and 3D intestinal in vitro models
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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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- Conference Paper
- C3
- open access
Unexpected formation of N-(chloromethyl)acetamides during attempted Staudinger β-lactam synthesis
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- Journal Article
- A1
- open access
Carboxylic acid bioisosteres in medicinal chemistry : synthesis and properties
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- Journal Article
- A1
- open access
Identification of mercaptoacetamide-based HDAC6 inhibitors via a lean inhibitor strategy : screening, synthesis, and biological evaluation
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- Journal Article
- A1
- open access
Covalent organic framework supported palladium catalysts
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The ubiquitin binding domain of HDAC6 : a key regulator of aggresomal protein disposal and new therapeutic target to combat multiple myeloma
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Fight against AMR : synthesis of pyrrolidine-fused azetidin-2-ones as potential antibacterials
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- Conference Paper
- C3
- open access
The ubiquitin binding domain of HDAC6 : a key regulator of aggresomal protein disposal and new therapeutic target to combat multiple myeloma
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The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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Curcumin-derived functionalized thiazepanes to selectively target colon cancer cells
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Curcumin-derived functionalized thiazepanes to selectively target colon cancer cells
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Unexpected formation of 2,2‐Dichloro‐N‐(chloromethyl)acetamides during attempted Staudinger 2,2‐Dichloro‐β‐lactam synthesis
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- Journal Article
- A1
- open access
Evolution of phosphorylases from N-acetylglucosaminide hydrolases in family GH3
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- Journal Article
- A1
- open access
Recent contributions of quinolines to antimalarial and anticancer drug discovery research
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Synthesis of novel nitroxoline analogs with potent cathepsin B exopeptidase inhibitory activity
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- Journal Article
- A1
- open access
Synthesis and biological evaluation of novel quinoline-piperidine scaffolds as antiplasmodium agents
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- Journal Article
- A1
- open access
A de novo synthetic method to the access of N-substituted benzazepines
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- Journal Article
- A1
- open access
Expedient synthesis of lupulones and their derivatization to 2,8-7H-dihydrochromen-7-ones
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- Journal Article
- A1
- open access
Synthetic strategies in curcumin chemistry focused on anticancer applications
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Design and synthesis of novel ferrocene-quinoline conjugates and evaluation of their electrochemical and antiplasmodium properties
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Synthesis and penicillin‐binding protein inhibitory assessment of dipeptidic 4‐phenyl‐β‐lactams from α‐amino acid‐derived imines
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- Journal Article
- A1
- open access
Deployment of aziridines for the synthesis of alkaloids and their derivatives
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- Journal Article
- A1
- open access
Synthesis of indoline‐based benzhydroxamic acids as potential HDAC6 inhibitors
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- Journal Article
- A1
- open access
α‐Unsaturated 3‐Amino‐1‐carboxymethyl‐β‐lactams as bacterial PBP inhibitors : synthesis and biochemical assessment
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- Journal Article
- A1
- open access
Synthesis of non‐symmetrical nitrogen‐containing curcuminoids in the pursuit of new anticancer candidates
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- Journal Article
- A1
- open access
Synthesis of 1,4‐thiazepane‐based curcuminoids with promising anticancer activity
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- Journal Article
- A1
- open access
Synthesis and cytotoxic evaluation of monocarbonyl curcuminoids and their pyrazoline derivatives
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- Journal Article
- A1
- open access
Electrophilic bromination in flow : a safe and sustainable alternative to the use of molecular bromine in batch
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Selective pharmacological inhibitors of HDAC6 reveal biochemical activity but functional tolerance in cancer models
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Reactivity of 3-oxo-β-lactams with respect to primary amines
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Reactivity of 3-oxo-β-lactams with respect to primary amines
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Use of 3-hydroxy-4-(trifluoromethyl)azetidin-2-ones as building blocks for the preparation of trifluoromethyl-containing aminopropanes, 1,3-oxazinan-2-ones, aziridines, and 1,4-dioxan-2-ones
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Theoretical insight into the regioselective ring-expansions of bicyclic aziridinium ions
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- Conference Paper
- C3
- open access
Synthesis of nitrogen-containing curcumin analogues in the pursuit of new anticancer candidates
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Formation of fluorinated amido esters through unexpected C3-C4 bond fission in 4-trifluoromethyl-3-oxo-β-lactams
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- Journal Article
- A1
- open access
Synthesis and reactivity of 4-(trifluoromethyl)azetidin-2-ones
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- Journal Article
- A1
- open access
Synthesis of Novel Aza‐aromatic Curcuminoids with Improved Biological Activities towards Various Cancer Cell Lines
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Exploring the sequence diversity in glycoside hydrolase family 13_18 reveals a novel glucosylglycerol phosphorylase
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- Journal Article
- A1
- open access
In silico design and enantioselective synthesis of functionalized monocyclic 3-amino-1-carboxymethyl-β-lactams as inhibitors of penicillin-binding proteins of resistant bacteria
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- Journal Article
- A1
- open access
Chemoenzymatic approach toward the synthesis of 3-O-(α/β)-glucosylated 3-hydroxy-β-lactams