about
3-Aminopyrazole inhibitors of CDK2/cyclin A as antitumor agents. 1. Lead findingEnabling technologies and green processes in cyclodextrin chemistryFirst Cdc7 kinase inhibitors: pyrrolopyridinones as potent and orally active antitumor agents. 2. Lead discoveryDesign and Synthesis of a γ(1)β(8)-Cyclodextrin Oligomer: A New Platform with Potential Application as a Dendrimeric Multicarrier.Complexes of peracetylated cyclodextrin in a non-aqueous aprotic medium: the role of residual water.Derivatization reactions of heterocyclic scaffolds on solid phase: tools for the synthesis of drug-like molecule libraries.Synthesis, characterization and potential application of monoacyl-cyclodextrins.Pd/C-catalyzed aerobic oxidative esterification of alcohols and aldehydes: a highly efficient microwave-assisted green protocol.A novel SWCNT platform bearing DOTA and β-cyclodextrin units. "One shot" multidecoration under microwave irradiation.Combined Microwaves/Ultrasound, a Hybrid Technology.Cdc7 kinase inhibitors: 5-heteroaryl-3-carboxamido-2-aryl pyrroles as potential antitumor agents. 1. Lead finding.Cdc7 kinase inhibitors: pyrrolopyridinones as potential antitumor agents. 1. Synthesis and structure-activity relationships.One-pot sequential synthesis of isocyanates and urea derivatives via a microwave-assisted Staudinger-aza-Wittig reaction.Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins.New asymmetrical per-substituted cyclodextrins (2-O-methyl-3-O-ethyl- and 2-O-ethyl-3-O-methyl-6-O-t-butyldimethylsilyl-beta-derivatives) as chiral selectors for enantioselective gas chromatography in the flavour and fragrance field.Efficient microwave-assisted synthetic protocols and in silico behaviour prediction of per-substituted β-cyclodextrins.Microwave-Assisted Synthesis and Physicochemical Characterization of Tetrafuranylporphyrin-Grafted Reduced-Graphene Oxide.Surface modification and cellular uptake evaluation of Au-coated Ni80Fe20 nanodiscs for biomedical applications.Efficient synthetic protocols in glycerol under heterogeneous catalysis.High throughput mechanochemistry: application to parallel synthesis of benzoxazines.Solvent-free copper-catalyzed azide-alkyne cycloaddition under mechanochemical activation.A new class of cationic cyclodextrins: synthesis and chemico-physical propertiesAmino derivatives of PEEK-WCImproving the esterification activity of Pseudomonas fluorescens and Burkholderia cepacia lipases via cross-linked cyclodextrin immobilizationCyclodextrin nanosponges as effective gas carriersInclusion of cinnamaldehyde in modified γ-cyclodextrinsCyclodextrin-Grafted Silica-Supported Pd Nanoparticles: An Efficient and Versatile Catalyst for Ligand-Free C−C Coupling and HydrogenationEfficient Green Protocols for Preparation of Highly Functionalized β-Cyclodextrin-Grafted SilicaFirst Cdc7 Kinase Inhibitors: Pyrrolopyridinones as Potent and Orally Active Antitumor Agents. 2. Lead DiscoveryEco-Friendly Physical Activation Methods for Suzuki–Miyaura ReactionsMicrowave-Assisted, Green Synthesis of 4(3H)-Quinazolinones under CO Pressure in γ-Valerolactone and Reusable Pd/β-Cyclodextrin Cross-Linked CatalystSelective hydrogenation of alkynes over ppm-level Pd/boehmite/Al2O3 beads in a continuous-flow reactorNucleophilic Substitutions of 6I-O-Monotosyl-β-cyclodextrin in a Planetary Ball MillRecent advances and perspectives in the synthesis of bioactive coumarinsHighly Efficient Mechanochemical N-Arylation of Amino Alcohols and Diamines with Cu0 PowderHighly Efficient Microwave-Assisted CO Aminocarbonylation with a Recyclable Pd(II)/TPP-β-Cyclodextrin Cross-Linked CatalystInterplay Between Mechanochemistry and SonochemistryOrganisation and complexation of mono-and bis-β-cyclodextrins without chromophores with a fluorescence-sensitive probe in aqueous solutionsPredicting self-assembly and structure in diluted aqueous solutions of modified mono- and bis-β-cyclodextrins that contain naphthoxy chromophore groupsSoluble cyanine dye/β-cyclodextrin derivatives: Potential carriers for drug delivery and optical imaging
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P50
description
researcher ORCID ID = 0000-0003-2256-5021
@en
wetenschapper
@nl
name
K Martina
@nl
Katia Martina
@en
Katia Martina
@es
type
label
K Martina
@nl
Katia Martina
@en
Katia Martina
@es
altLabel
K Martina
@en
prefLabel
K Martina
@nl
Katia Martina
@en
Katia Martina
@es
P106
P1153
22235080700
P21
P31
P496
0000-0003-2256-5021