Works matching AU D'hooghe, Matthias
Results: 36
Use of functionalized β-lactams as building blocks in heterocyclic chemistry.
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- Pure & Applied Chemistry, 2010, v. 82, n. 9, p. 1749, doi. 10.1351/PAC-CON-09-09-39
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- Article
Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments.
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- ChemistryOpen, 2023, v. 12, n. 2, p. 1, doi. 10.1002/open.202200262
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Expedient Synthesis of Lupulones and Their Derivatization to 2,8‐7H‐Dihydrochromen‐7‐ones.
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- ChemistryOpen, 2020, v. 9, n. 4, p. 442, doi. 10.1002/open.202000008
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Synthesis of Novel Aza‐aromatic Curcuminoids with Improved Biological Activities towards Various Cancer Cell Lines.
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- ChemistryOpen, 2018, v. 7, n. 5, p. 381, doi. 10.1002/open.201800029
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Synthetic Approaches toward Monocyclic 3-Amino-β-lactams.
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- ChemistryOpen, 2017, v. 6, n. 3, p. 301, doi. 10.1002/open.201700051
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Engineering Comamonas testosteroni for the production of 2-pyrone-4,6-dicarboxylic acid as a promising building block.
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- Microbial Cell Factories, 2023, v. 22, n. 1, p. 1, doi. 10.1186/s12934-023-02202-2
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Synthesis of Pyrrolidine‐fused β‐lactams as Potential β‐lactamase Inhibitors.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 11, p. 1, doi. 10.1002/ajoc.202400364
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Synthesis and Applications of 3-Methylene-4- (trifluoromethyl)azetidin-2-ones as Building Blocks for the Preparation of Mono- and Spirocyclic 4-CF<sub>3</sub>-β-Lactams.
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- Asian Journal of Organic Chemistry, 2016, v. 5, n. 12, p. 1480, doi. 10.1002/ajoc.201600387
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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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- Chemistry - An Asian Journal, 2020, v. 15, n. 1, p. 51, doi. 10.1002/asia.201901470
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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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- Chemistry - An Asian Journal, 2018, v. 13, n. 4, p. 421, doi. 10.1002/asia.201701636
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Nucleophile-Dependent Regio- and Stereoselective Ring Opening of 1-Azoniabicyclo[3.1.0]hexane Tosylate.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 4, p. 1060, doi. 10.1002/asia.201301551
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Conjugate addition of 2-(bromomethyl)- and 2-(2-bromoethyl)-piperidine to alkyl acrylates: application towards the synthesis of 2-(methoxycarbonyl)indolizidine.
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- ARKIVOC: Online Journal of Organic Chemistry, 2010, p. 93
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Antibacterial and β‐Lactamase Inhibitory Activity of Monocyclic β‐Lactams.
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- Medicinal Research Reviews, 2018, v. 38, n. 2, p. 426, doi. 10.1002/med.21443
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Synthesis of Indoline‐Based Benzhydroxamic Acids as Potential HDAC6 Inhibitors.
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- ChemistrySelect, 2019, v. 4, n. 42, p. 12308, doi. 10.1002/slct.201902042
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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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- European Journal of Organic Chemistry, 2021, v. 2021, n. 42, p. 5823, doi. 10.1002/ejoc.202100975
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Carbonylation of Aziridines as a Powerful Tool for the Synthesis of Functionalized β-Lactams.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 40, p. 5943, doi. 10.1002/ejoc.201700698
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LiAlH<sub>4</sub>-Induced Thia-Aza-Payne Rearrangement of Functionalized 2-(Thiocyanatomethyl)aziridines into 2-(Aminomethyl)thiiranes as an Entry to 5-(Chloromethyl)thiazolidin-2-ones.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 22, p. 3229, doi. 10.1002/ejoc.201700549
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Carboxylic Acid Bioisosteres in Medicinal Chemistry: Synthesis and Properties.
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- Journal of Chemistry, 2022, p. 1, doi. 10.1155/2022/2164558
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Synthesis of Novel Nitroxoline Analogs with Potent Cathepsin B Exopeptidase Inhibitory Activity.
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- ChemMedChem, 2020, v. 15, n. 24, p. 2477, doi. 10.1002/cmdc.202000402
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Bicyclic Aziridinium Ions in Azaheterocyclic Chemistry - Preparation and Synthetic Application of 1-Azoniabicyclo[n.1.0]alkanes.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 22, p. 3485, doi. 10.1002/adsc.201600750
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Front Cover Picture: Bicyclic Aziridinium Ions in Azaheterocyclic Chemistry - Preparation and Synthetic Application of 1-Azoniabicyclo[n.1.0]alkanes (Adv. Synth. Catal. 22/2016).
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 22, p. 3483, doi. 10.1002/adsc.201601081
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Electrophilic Bromination in Flow: A Safe and Sustainable Alternative to the Use of Molecular Bromine in Batch.
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- Molecules, 2019, v. 24, n. 11, p. 2116, doi. 10.3390/molecules24112116
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Selective pharmacological inhibitors of HDAC6 reveal biochemical activity but functional tolerance in cancer models.
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- International Journal of Cancer, 2019, v. 145, n. 3, p. 735, doi. 10.1002/ijc.32169
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α‐Unsaturated 3‐Amino‐1‐carboxymethyl‐β‐lactams as Bacterial PBP Inhibitors: Synthesis and Biochemical Assessment.
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- Chemistry - A European Journal, 2019, v. 25, n. 70, p. 16128, doi. 10.1002/chem.201904139
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Synthesis of 1,4‐Thiazepane‐Based Curcuminoids with Promising Anticancer Activity.
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- Chemistry - A European Journal, 2019, v. 25, n. 54, p. 12583, doi. 10.1002/chem.201902549
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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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- Chemistry - A European Journal, 2018, v. 24, n. 57, p. 15254, doi. 10.1002/chem.201801868
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Reactivity of 3-Oxo-β-lactams with Respect to Primary Amines-An Experimental and Computational Approach.
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- Chemistry - A European Journal, 2017, v. 23, n. 71, p. 18002, doi. 10.1002/chem.201703852
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Synthesis of Potent and Selective HDAC6 Inhibitors Bearing a Cyclohexane- or Cycloheptane-Annulated 1,5-Benzothiazepine Scaffold.
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- Chemistry - A European Journal, 2017, v. 23, n. 1, p. 128, doi. 10.1002/chem.201604167
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LiAlH<sub>4</sub>-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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- Chemistry - A European Journal, 2016, v. 22, n. 14, p. 4945, doi. 10.1002/chem.201504853
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Selective Synthesis of Functionalized Trifluoromethylated Pyrrolidines, Piperidines, and Azepanes Starting from 1-Tosyl-2-(trifluoromethyl)aziridine.
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- Chemistry - A European Journal, 2014, v. 20, n. 34, p. 10650, doi. 10.1002/chem.201304759
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Nucleophile-Directed Selective Transformation of cis-1-Tosyl-2-tosyloxymethyl-3-(trifluoromethyl)aziridine into Aziridines, Azetidines, and Benzo-Fused Dithianes, Oxathianes, Dioxanes, and (Thio)morpholines.
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- Chemistry - A European Journal, 2013, v. 19, n. 19, p. 5966, doi. 10.1002/chem.201204485
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Synthesis of 2-Hydroxy-1,4-oxazin-3-ones through Ring Transformation of 3-Hydroxy-4-(1,2-dihydroxyethyl)-β-lactams and a Study of Their Reactivity.
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- Chemistry - A European Journal, 2013, v. 19, n. 10, p. 3383, doi. 10.1002/chem.201203314
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Highly Stereoselective Synthesis of β-Lactams Utilizing α-Chloroimines as New and Powerful Chiral Inductors.
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- Chemistry - A European Journal, 2008, v. 14, n. 21, p. 6336, doi. 10.1002/chem.200800845
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- Article
High-yield synthesis of 2-O-α-d-glucosyl-d-glycerate by a bifunctional glycoside phosphorylase.
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- Applied Microbiology & Biotechnology, 2024, v. 108, n. 1, p. 1, doi. 10.1007/s00253-023-12970-x
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High-yield synthesis of 2-O-α-d-glucosyl-d-glycerate by a bifunctional glycoside phosphorylase.
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- Applied Microbiology & Biotechnology, 2024, v. 108, n. 1, p. 1, doi. 10.1007/s00253-023-12970-x
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Synthesis of 4‐imidoyl‐, 4‐oxiranyl‐ and 4‐propargyloxyphenyl‐substituted β‐lactam building blocks.
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- Journal of Heterocyclic Chemistry, 2023, v. 60, n. 3, p. 423, doi. 10.1002/jhet.4597
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