about
Synthesis and TNF expression inhibitory properties of new thalidomide analogues derived via Heck cross coupling.Rapid evaluation of Antrodia camphorata natural products and derivatives in tumourigenic liver progenitor cells with a novel cell proliferation assay.New thalidomide analogues derived through Sonogashira or Suzuki reactions and their TNF expression inhibition profiles.Pd(II) conjugated chitosan nanofibre mats for application in Heck cross-coupling reactions.Identification of a thalidomide derivative that selectively targets tumorigenic liver progenitor cells and comparing its effects with lenalidomide and sorafenib.The synthesis and biological activity of novel anthracenone-pyranones and anthracenone-furans.The antiplasmodial activity of norcantharidin analogs.Efforts toward elucidating Thalidomide's molecular target: an expedient synthesis of the first Thalidomide biotin analogue.Formation and reactions of azepino[4,5-b]indoles: an unprecedented ozone reaction in the formation of novel benzo[c]naphthyridinones.Fluorescent triphenyl substituted maleimide derivatives: synthesis, spectroscopy and quantum chemical calculations.Domino Heck-aza-Michael reactions: efficient access to 1-substituted tetrahydro-beta-carbolines.Towards a total synthesis of the new anticancer agent mensacarcin: synthesis of the carbocyclic core.Inspiration from old dyes: tris(stilbene) compounds as potent gram-positive antibacterial agents.Metabolic transformation has a profound effect on anti-inflammatory activity of flavonoids such as quercetin: lack of association between antioxidant and lipoxygenase inhibitory activity.Enantioselective Synthesis of anti-1,2-Oxaborinan-3-enes from Aldehydes and 1,1-Di(boryl)alk-3-enes Using Ruthenium and Chiral Phosphoric Acid Catalysts.Synthesis of Enantiopure C3 -Symmetric Triangular Molecules.Palladium-catalyzed dicarbonylative synthesis of tetracycle quinazolinones.Spectrum of antibacterial activity and mode of action of a novel tris-stilbene bacteriostatic compound.Transition Metal-free Methylation of Amines with Formaldehyde as the Reductant and Methyl SourceHeterocyclic substituted cantharidin and norcantharidin analogues—synthesis, protein phosphatase (1 and 2A) inhibition, and anti-cancer activityNorcantharimides, synthesis and anticancer activity: Synthesis of new norcantharidin analogues and their anticancer evaluationSynthesis and biological evaluation of norcantharidin analogues: Towards PP1 selectivityN6-(5,6-epoxynorbornyl)adenosine analogs as A1 adenosine agonistsA general approach to N-heterocyclic scaffolds using domino Heck-aza-Michael reactionsDomino reactions for the synthesis of anthrapyran-2-ones and the total synthesis of the natural product (±)-BE-26554ATris(tri-o-tolyl phosphite-κP)nickel: a coordinatively unsaturated nickel(0) complexStereoselective synthesis of 2,3-dihydropyrroles from terminal alkynes, azides, and α,β-unsaturated aldehydes via N-sulfonyl-1,2,3-triazolesNickel Phosphite/Phosphine-Catalyzed C-S Cross-Coupling of Aryl Chlorides and ThiolsA One-Pot Reaction of α-Imino Rhodium Carbenoids and Halohydrins: Access to 2,6-Substituted Dihydro-2H-1,4-oxazinesHeterologous biosynthesis of elsinochrome A sheds light on the formation of the photosensitive perylenequinone systemAsymmetric Synthesis and Stereochemical Assignment of 12C/13C Isotopomers
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Scott G. Stewart
@ast
Scott G. Stewart
@en
Scott G. Stewart
@es
Scott G. Stewart
@nl
Scott G. Stewart
@sl
type
label
Scott G. Stewart
@ast
Scott G. Stewart
@en
Scott G. Stewart
@es
Scott G. Stewart
@nl
Scott G. Stewart
@sl
prefLabel
Scott G. Stewart
@ast
Scott G. Stewart
@en
Scott G. Stewart
@es
Scott G. Stewart
@nl
Scott G. Stewart
@sl
P106
P1153
7401747026
P21
P31
P496
0000-0002-7537-247X