Micah Maetani

Affiliations: 
Harvard University, Cambridge, MA, United States 
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"Micah Maetani"
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Li W, Garcia-Rivera EM, Mitchell DC, et al. (2024) Highly specific intracellular ubiquitination of a small molecule. Biorxiv : the Preprint Server For Biology
Melillo B, Zoller J, Hua BK, et al. (2018) Synergistic effects of stereochemistry and appendages on the performance diversity of a collection of synthetic compounds. Journal of the American Chemical Society
Verho O, Maetani M, Melillo B, et al. (2017) Stereospecific Palladium-Catalyzed C-H Arylation of Pyroglutamic Acid Derivatives at the C3 Position Enabled by 8-Aminoquinoline as a Directing Group. Organic Letters
Maetani M, Zoller J, Melillo B, et al. (2017) Synthesis of a bicyclic azetidine with in vivo antimalarial activity enabled by stereospecific, directed C(sp(3))-H arylation. Journal of the American Chemical Society
Maetani M, Kato N, Jabor VAP, et al. (2017) Discovery of Antimalarial Azetidine-2-carbonitriles That Inhibit P. falciparum Dihydroorotate Dehydrogenase. Acs Medicinal Chemistry Letters. 8: 438-442
Kato N, Comer E, Sakata-Kato T, et al. (2016) Diversity-oriented synthesis yields novel multistage antimalarial inhibitors. Nature
Swann J, Corey V, Scherer CA, et al. (2016) High-Throughput Luciferase-Based Assay for the Discovery of Therapeutics That Prevent Malaria. Acs Infectious Diseases. 2: 281-293
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