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Toward Structural Correctness: Aquatolide and the Importance of 1D Proton NMR FID ArchivingPlastidial metabolite MEcPP induces a transcriptionally centered stress-response hub via the transcription factor CAMTA3Comparison of small molecule inhibitors of the bacterial cell division protein FtsZ and identification of a reliable cross-species inhibitor.A structurally diverse library of polycyclic lactams resulting from systematic placement of proximal functional groups.N-Benzyl-3-sulfonamidopyrrolidines as novel inhibitors of cell division in E. coli.Naturally diverse: highlights in versatile synthetic methods enabling target- and diversity-oriented synthesis.Recent advances in multicomponent reactions for diversity-oriented synthesis.Gyramides prevent bacterial growth by inhibiting DNA gyrase and altering chromosome topology.Diastereoselective magnesium halide-catalyzed anti-aldol reactions of chiral N-acyloxazolidinones.Magnesium halide-catalyzed anti-aldol reactions of chiral N-acylthiazolidinethiones.Synthesis of a γ-lactam library via formal cycloaddition of imines and substituted succinic anhydrides.Failsafe mechanisms couple division and DNA replication in bacteria.Synthesis of a library of "lead-like" γ-lactams by a one pot, four-component reactionPractical synthesis of PC190723, an inhibitor of the bacterial cell division protein FtsZ.Zinc-catalyzed silylation of terminal alkynes.Ammonia synthons for the multicomponent assembly of complex gamma-lactams.N-Benzyl-3-sulfonamidopyrrolidines are a New Class of Bacterial DNA Gyrase Inhibitors.Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZDirect displacement of alkoxy groups of vinylogous esters by Grignard reagents.Synthesis of the diaryl ether cores common to chrysophaentins A, E and F.Characterization of Caulobacter crescentus FtsZ protein using dynamic light scatteringSynthesis of 6,6'-binaphthopyran-2-one natural products: pigmentosin A, talaroderxines A and B.Preparation of a conjugation-ready thiol responsive molecular switch.Chemical inhibition of the mitochondrial division dynamin reveals its role in Bax/Bak-dependent mitochondrial outer membrane permeabilizationFrom bead to flask: Synthesis of a complex β-amido-amide for probe-development studies.Synthesis of antimicrobial natural products targeting FtsZ: (+/-)-dichamanetin and (+/-)-2' ''-hydroxy-5' '-benzylisouvarinol-B.Mechanism of alkoxy groups substitution by Grignard reagents on aromatic rings and experimental verification of theoretical predictions of anomalous reactionsDesign and synthesis of mimics of the T7-loop of FtsZ.Identification of the molecular target of small molecule inhibitors of HDL receptor SR-BI activity.Synthesis and hybridization property of an oligonucleotide containing a 3-thioformacetal linked pentathymidylate.Diastereoselective synthesis of γ- and δ-lactams from imines and sulfone-substituted anhydrides.Targeting the Bacterial Division Protein FtsZ.Stereocontrol in asymmetric γ-lactam syntheses from imines and cyanosuccinic anhydrides.Inhibitors of bacterial tubulin target bacterial membranes in vivoCatalytic Alkene Cyclization Reactions for the Stereoselective Synthesis of Complex "Terpenoid-like" Heterocycles.The Synthesis and Antimicrobial Activity of Heterocyclic Derivatives of Totarol.Synthesis of (-)-viriditoxin: a 6,6'-binaphthopyran-2-one that targets the bacterial cell division protein FtsZ.Enantioselective synthesis of isotopically labeled homocitric acid lactone.Second-Generation Synthesis of (-)-Viriditoxin.Stereoselective synthesis of γ-lactams from imines and cyanosuccinic anhydrides.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jared Shaw
@ast
Jared Shaw
@en
Jared Shaw
@es
Jared Shaw
@nl
Jared Shaw
@sl
type
label
Jared Shaw
@ast
Jared Shaw
@en
Jared Shaw
@es
Jared Shaw
@nl
Jared Shaw
@sl
prefLabel
Jared Shaw
@ast
Jared Shaw
@en
Jared Shaw
@es
Jared Shaw
@nl
Jared Shaw
@sl
P108
P106
P1153
7403898693
P21
P31
P496
0000-0001-5190-493X