Jennifer R. Mazzone, Ph.D.
Affiliations: | 2011 | University of New Hampshire, Durham, NH, United States |
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Organic ChemistryGoogle:
"Jennifer Mazzone"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Charles Kent Zercher | grad student | 2011 | UNH | |
| (I. The synthesis of papyracillic acids: Application of the tandem chain extension-acylation reaction. II. Diastereoselective synthesis of beta-methyl-gamma-keto esters through the utility of an L-serine auxiliary.) | ||||
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| Henderson CS, Mazzone JR, Moore AM, et al. (2021) Tandem Homologation-Acylation Chemistry: Single and Double Homologation. Tetrahedron. 91 |
| Roy S, Kapoor A, Zhu F, et al. (2020) Artemisinins target the intermediate filament protein vimentin for human cytomegalovirus inhibition. The Journal of Biological Chemistry |
| Fox JM, Moynihan JR, Mott BT, et al. (2016) Artemisinin-derived dimer ART-838 potently inhibited human acute leukemias, persisted in vivo, and synergized with antileukemic drugs. Oncotarget |
| Conyers RC, Mazzone JR, Tripathi AK, et al. (2015) Antimalarial chemotherapy: orally curative artemisinin-derived trioxane dimer esters. Bioorganic & Medicinal Chemistry Letters. 25: 245-8 |
| Mazzone JR, Conyers RC, Tripathi AK, et al. (2014) Antimalarial chemotherapy: artemisinin-derived dimer carbonates and thiocarbonates. Bioorganic & Medicinal Chemistry Letters. 24: 2440-3 |
| Conyers RC, Mazzone JR, Siegler MA, et al. (2014) The survival times of malaria-infected mice are prolonged more by several new two-carbon-linked artemisinin-derived dimer carbamates than by the trioxane antimalarial drug artemether. Bioorganic & Medicinal Chemistry Letters. 24: 1285-9 |
| Mazzone JR, Zercher CK. (2012) Syntheses of papyracillic acids: Application of the tandem chain extension-acylation reaction Journal of Organic Chemistry. 77: 9171-9178 |
| Jacobine AM, Mazzone JR, Slack RD, et al. (2012) Malaria-infected mice live until at least day 30 after a new artemisinin-derived thioacetal thiocarbonate combined with mefloquine are administered together in a single, low, oral dose. Journal of Medicinal Chemistry. 55: 7892-9 |