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Irreversible inhibitors of the proline racemase unveil innovative mechanism of action as antibacterial agents against Clostridioides difficile.
- Published in:
- Chemical Biology & Drug Design, 2022, v. 99, n. 4, p. 513, doi. 10.1111/cbdd.14005
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- Article
Designed mono- and di-covalent inhibitors trap modeled functional motions for Trypanosoma cruzi proline racemase in crystallography.
- Published in:
- PLoS Neglected Tropical Diseases, 2018, v. 12, n. 10, p. 1, doi. 10.1371/journal.pntd.0006853
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- Article
Reactivity of N-Boc-Protected Amino-Ynones in the Presence of Zinc Chloride: Formation of Acetylenic Cyclic Imines and Their Palladium Complexes.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 22, p. 4868, doi. 10.1002/ejoc.201500569
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- Article
Methanesulfonic Acid Mediated Cyclization and Meyer-Schuster Rearrangement of γ-Amino-ynones: Access to Enantiopure Pyrrolidine Exocyclic Vinylogous Amides.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 21, p. 4506, doi. 10.1002/ejoc.201402336
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- Article
From Aspartic Acid to Dihydropyridone-2-carboxylates: Access to Enantiopure 6-Substituted 4-Oxo- and 4-Hydroxypipecolic Acid Derivatives.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 29, p. 6677, doi. 10.1002/ejoc.201300812
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- Article
Combined Approaches for Drug Design Points the Way to Novel Proline Racemase Inhibitor Candidates to Fight Chagas’ Disease.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060955
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- Article
Synthese de dihydro-6,7 benzo- b [1 H] azonines par extension de cycle de dihydro-4,5 benzo- b [1 H] azepines.
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- Journal of Heterocyclic Chemistry, 1989, v. 26, n. 6, p. 1719, doi. 10.1002/jhet.5570260637
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- Article