David F. Wiemer

Affiliations: 
Chemistry University of Iowa, Iowa City, IA 
Area:
Organic Chemistry, Biochemistry
Website:
https://chem.uiowa.edu/people/david-f-wiemer
Google:
"David Francis Wiemer"
Bio:

DOI: 10.1021/acsmedchemlett.7b00245

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Parents

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Nelson J. Leonard grad student 1976 UIUC
 (Chemical and radiative modification of nucleic acid bases)
Jerrold Meinwald post-doc 1976-1978 Cornell
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Publications

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Stockdale DP, Beutler JA, Wiemer DF. (2022) Substitution of a triazole for the central olefin in biologically active stilbenes. Bioorganic & Medicinal Chemistry Letters. 128980
Schroeder CM, Dey PN, Beutler JA, et al. (2021) Synthesis of a Coumarin-Based Analogue of Schweinfurthin F. The Journal of Organic Chemistry
Harmon NM, Huang X, Schladetsch MA, et al. (2020) Potent double prodrug forms of synthetic phosphoantigens. Bioorganic & Medicinal Chemistry. 28: 115666
Goetz DB, Varney ML, Wiemer DF, et al. (2020) Amides as bioisosteres of triazole-based geranylgeranyl diphosphate synthase inhibitors. Bioorganic & Medicinal Chemistry. 28: 115604
Bhuiyan NH, Varney ML, Wiemer DF, et al. (2019) Novel benzimidazole phosphonates as potential inhibitors of protein prenylation. Bioorganic & Medicinal Chemistry Letters. 126757
Li J, Lentini NA, Wiemer DF, et al. (2019) A luciferase lysis assay reveals in vivo malignant cell sensitization by phosphoantigen prodrugs. Biochemical Pharmacology. 113668
Lentini NA, Hsiao CC, Crull GB, et al. (2019) Synthesis and Bioactivity of the Alanyl Phosphonamidate Stereoisomers Derived from a Butyrophilin Ligand. Acs Medicinal Chemistry Letters. 10: 1284-1289
Bhuiyan NH, Varney ML, Bhattacharya DS, et al. (2019) ω-Hydroxy isoprenoid bisphosphonates as linkable GGDPS inhibitors. Bioorganic & Medicinal Chemistry Letters. 126633
Foust BJ, Li J, Hsiao CC, et al. (2019) Stability and Efficiency of Mixed Aryl Phosphonate Prodrugs. Chemmedchem
Lentini N, Foust BJ, Hsiao CC, et al. (2018) Phosphonamidate prodrugs of a butyrophilin ligand display plasma stability and potent Vγ9Vδ2 T cell stimulation. Journal of Medicinal Chemistry
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