Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Lacey Hizartzidis"'
Autor:
Ahmed Al Otaibi, Adam McCluskey, Cecilia C. Russell, Lacey Hizartzidis, Fiona M. Deane, Jennette A. Sakoff, Siobhann N. McCluskey
Publikováno v:
RSC Advances. 9:7652-7663
The Ugi four component reaction of an aldehyde, amine, isocyanide and an ethanoic acid was effected smoothly in protic ionic liquids ethylammonium nitrate (EAN) and propylammonium nitrate (PAN) to afford analogues of α-phenylacetamido amides in good
Publikováno v:
ChemMedChem. 14(12)
Octahydroepoxyisoindole analogues of norcantharidin were accessed through a Diels-Alder reaction of an amine-substituted furan with maleic anhydride and subsequent reduction of the bicyclo[2.2.1]heptene olefin. Despite retention of the carboxylate an
Publikováno v:
Organic & Biomolecular Chemistry. 13:7119-7130
There has been an increasing body of evidence that flow hydrogenation enhances reduction outcomes across a wide range of synthetic transformations. Moreover flow reactors enhance laboratory safety with pyrophoric catalysts contained in sealed cartrid
Autor:
Adam McCluskey, Christopher P. Gordon, Lacey Hizartzidis, Mark J. Robertson, Michela I. Simone, Kelly A. Young, Peter J. Cossar
Publikováno v:
RSC Adv.. 4:56743-56748
A commonly observed limitation of conducting hydrogenations under flow chemistry conditions is hydrodehalogenation. In a bid to circumvent this limitation a series of hydrogenation catalysts were screened, with 5% Pt/C (sulfided) catalyst identified
Autor:
Christopher P. Gordon, Lacey Hizartzidis, Jennette A. Sakoff, Bronwyn E. Campbell, Robin B. Gasser, Jayne Gilbert, Mark Tarleton, Adam McCluskey
Publikováno v:
Med. Chem. Commun.. 5:159-164
We report the discovery of a series of acrylonitrile-containing molecules and α-amino amides which cause 99–100% lethality in H. contortus. Of the 22 acrylonitrile analogues investigated, the most active were 2-cyano-3-[1-(3-dimethylaminopropyl)-2
Publikováno v:
ChemInform. 46
There has been an increasing body of evidence that flow hydrogenation enhances reduction outcomes across a wide range of synthetic transformations. Moreover flow reactors enhance laboratory safety with pyrophoric catalysts contained in sealed cartrid
Autor:
Trieu N. Trinh, David G. Harman, Lacey Hizartzidis, Christopher P. Gordon, Andrew J. S. Lin, Adam McCluskey
Publikováno v:
Organicbiomolecular chemistry. 12(47)
Suzuki cross-couplings of 5-formyl-2-furanylboronic acid with activated or neutral aryl bromides were performed under continuous flow conditions in the presence of (Bu)4N(+)F(-) and the immobilised t-butyl based palladium catalyst CatCart™ FC1032
Publikováno v:
ChemInform. 45
Two series (VI) and (XI) of norcantharidin analogues are synthesized using continuous flow hydrogenation in key steps.
Publikováno v:
ChemInform. 42
Four-component Ugi—Knoevenagel reaction of o-aminophenyl ketones (I) with aromatic aldehydes, cyanoacetic acid and isonitriles provides access towards polyfunctionalized quinolinones, e.g. (V) and (IX).
Publikováno v:
RSC Advances. 4:9709
Two libraries of highly decorated norcantharidin analogues were accessed via a series of sequential chemoselective flow hydrogenations and solvent-free transformations. Utilising a 10% Pd/C catalyst, modifications to reaction parameters (H2 pressure,