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A Critical Study on Acylating and Covalent Reversible Fragment Inhibitors of SARS‐CoV‐2 Main Protease Targeting the S1 Site with Pyridine.
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- ChemMedChem, 2023, v. 18, n. 9, p. 1, doi. 10.1002/cmdc.202200635
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Chemical Evolution of Antivirals Against Enterovirus D68 through Protein‐Templated Knoevenagel Reactions.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 24, p. 13294, doi. 10.1002/anie.202102074
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- Article
Chemische Evolution antiviraler Wirkstoffe gegen Enterovirus D68 durch Proteintemplat‐gesteuerte Knoevenagelreaktionen.
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- Angewandte Chemie, 2021, v. 133, n. 24, p. 13405, doi. 10.1002/ange.202102074
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Protein‐Templated Ugi Reactions versus In‐Situ Ligation Screening: Two Roads to the Identification of SARS‐CoV‐2 Main Protease Inhibitors.
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- Chemistry - A European Journal, 2024, v. 30, n. 17, p. 1, doi. 10.1002/chem.202303940
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- Article