Beth Knapp-Reed
Affiliations: | 2005-2006 | University of Michigan, Ann Arbor, Ann Arbor, MI |
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| Su DS, Qu J, Schulz M, et al. (2020) Discovery of Isoxazole Amides as Potent and Selective SMYD3 Inhibitors. Acs Medicinal Chemistry Letters. 11: 133-140 |
| Haffner CD, Charnley AK, Aquino CJ, et al. (2019) Discovery of Pyrazolocarboxamides as Potent and Selective Receptor Interacting Protein 2 (RIP2) Kinase Inhibitors. Acs Medicinal Chemistry Letters. 10: 1518-1523 |
| Morales-Ramos AI, Mecom JS, Kiesow TJ, et al. (2008) Tetrahydro-4-quinolinamines identified as novel P2Y(1) receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 18: 6222-6 |
| Chrovian CC, Knapp-Reed B, Montgomery J. (2008) Total synthesis of aigialomycin D: surprising chemoselectivity dependence on alkyne structure in nickel-catalyzed cyclizations. Organic Letters. 10: 811-4 |
| Knapp-Reed B, Mahandru GM, Montgomery J. (2005) Access to macrocyclic endocyclic and exocyclic allylic alcohols by nickel-catalyzed reductive cyclization of ynals. Journal of the American Chemical Society. 127: 13156-7 |
| Roush WR, Cheng J, Knapp-Reed B, et al. (2001) Potent second generation vinyl sulfonamide inhibitors of the trypanosomal cysteine protease cruzain. Bioorganic & Medicinal Chemistry Letters. 11: 2759-62 |