Jérémy Kister

Zionsville Community High School — United States

Chemistry · Physical Sciences

11h-index522citations31works0.02yr avg
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Research Topics

Asymmetric Synthesis and Catalysis(9), Synthetic Organic Chemistry Methods(7), Asymmetric Hydrogenation and Catalysis(5), Organoboron and organosilicon chemistry(5), Synthesis and biological activity(3)

Publications31 total

Improved synthetic route to quinoxyfen photometabolite 2‐chloro‐10‐fluorochromeno[2,3,4‐<i>de</i>]quinoline
Pest Management Science·2017· 1 cited
ChemInform Abstract: Enantio‐ and Diastereoselective Synthesis of syn‐β‐Hydroxy‐α‐vinyl Carboxylic Esters via Reductive Aldol Reactions of Ethyl Allenecarboxylate with 10‐TMS‐9‐Borabicyclo[3.3.2]decane and DFT Analysis of the Hydroboration Pathway.
ChemInform·2014
Enantio- and Diastereoselective Synthesis of <i>syn</i>-β-Hydroxy-α-vinyl Carboxylic Esters via Reductive Aldol Reactions of Ethyl Allenecarboxylate with 10-TMS-9-Borabicyclo[3.3.2]decane and DFT Analysis of the Hydroboration Pathway
Organic Letters·2013· 20 citedOpen Access
Optimization and Characterization of an Inhibitor for NADPH Oxidase 1 (NOX-1)
Europe PMC (PubMed Central)·2011· 12 cited
Figure 7, Treatment with compound 1 (ML171) significantly blocks ECM degradation in DLD1 cells
2011
Table 4, SAR Table of Phenothiazines
2011
Table 5, NIMH’s Psychoactive Drug Screening Program results for compound 1
2011· 1 cited
Table 1, Overview of PubChem assays for NOX1 inhibitor project
2011
Table 2, Compounds Submitted to the MLSMR
2011
Table 3, Selectivity of parent hit and probe compounds compared to that of chlorpromazine
2011
Figure 6, Compound 1 (ML171) treatment significantly blocks invadopodia formation in DLD1 cells
2011
Development of a double allylboration reagent targeting 1,5-syn-(E)-diols: application to the synthesis of the C(23)–C(40) fragment of tetrafibricin [Tetrahedron 67 (35) (2011) 6497–6512]
Tetrahedron·2011· 3 cited
ChemInform Abstract: A Synthetic Route to α‐Substituted Butenolides: Enantioselective Synthesis of (+)‐Ancepsenolide.
ChemInform·2011
Development of a double allylboration reagent targeting 1,5-syn-(E)-diols: application to the synthesis of the C(23)–C(40) fragment of tetrafibricin
Tetrahedron·2011· 25 citedOpen Access
ChemInform Abstract: Enantio‐ and Diastereoselective Synthesis of (E)‐1,5‐syn‐Diols: Application to the Synthesis of the C(23)—C(40) Fragment of Tetrafibricin.
ChemInform·2011
A Synthetic Route to α‐Substituted Butenolides: Enantioselective Synthesis of (+)‐Ancepsenolide
European Journal of Organic Chemistry·2011· 24 cited
Enantio- and Diastereoselective Synthesis of (<i>E</i>)-1,5-<i>syn</i>-Diols: Application to the Synthesis of the C(23)−C(40) Fragment of Tetrafibricin
Organic Letters·2011· 38 citedOpen Access
A Novel and Specific NADPH Oxidase-1 (Nox1) Small-Molecule Inhibitor Blocks the Formation of Functional Invadopodia in Human Colon Cancer Cells
ACS Chemical Biology·2010· 185 cited
ChemInform Abstract: Stereoselective Synthesis of γ‐Substituted (Z)‐Allylic Boranes via Kinetically Controlled Hydroboration of Allenes with 10‐TMS‐9‐Borabicyclo[3.3.2]decane.
ChemInform·2010
Origin of Thermodynamic versus Kinetic Control of Allene Hydroboration with 9-Borabicyclo[3.3.1]nonane and 10(R)-Trimethylsilyl-9-Borabicyclo[3.3.2]decane
Organic Letters·2009· 38 cited
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Frequent Co-authors

William Roush(11), SJ Brown(8), Hugh Rosen(7), Peter Hodder(7), Ricardo Lira(6), WR Roush(6), D Gianni(5), N Nicolas(5), C Der Mardirossian(5), GM Bokoch(5), Davide Gianni(4), Daniel H. Ess(4), Philippe Nuhant(4), Achim Sorg(4), Nayla Nicolas(3), C Der Mardirossian(3), GM Bokoch(3), Luis E. Martínez(2), Amy C. DeBaillie(2), Ming Chen(2)