Found: 7
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Baylis–Hillman adducts with molluscicidal activity against Biomphalaria glabrata.
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- Pest Management Science, 2006, v. 62, n. 3, p. 288, doi. 10.1002/ps.1153
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- Article
One-Electron Reduction Potentials: Calibration of Theoretical Protocols for Morita-Baylis-Hillman Nitroaromatic Compounds in Aprotic Media.
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- Molecules, 2018, v. 23, n. 9, p. 2129, doi. 10.3390/molecules23092129
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- Article
Morita-Baylis-Hillman Adducts Display Anti-Inflammatory Effects by Modulating Inflammatory Mediator Expression in RAW264.7 Cells.
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- Mediators of Inflammation, 2017, p. 1, doi. 10.1155/2017/6898505
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- Article
Morita–Baylis–Hillman adducts derived from thymol: synthesis, in silico studies and biological activity against Giardia lamblia.
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- Molecular Diversity, 2022, v. 26, n. 4, p. 1969, doi. 10.1007/s11030-021-10308-1
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- Article
Synthesis, anti-proliferative activity, theoretical and 1H NMR experimental studies of Morita–Baylis–Hillman adducts from isatin derivatives.
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- Molecular Diversity, 2020, v. 24, n. 1, p. 265, doi. 10.1007/s11030-019-09950-7
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- Article
<i>Trypanosoma cruzi</i> Cell Death Induced by the Morita-Baylis-Hillman Adduct 3-Hydroxy-2-Methylene-3-(4-Nitrophenylpropanenitrile).
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0093936
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- Article
Comparisons between Crystallography Data and Theoretical Parameters and the Formation of Intramolecular Hydrogen Bonds: Benznidazole.
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- Crystals (2073-4352), 2016, v. 6, n. 5, p. 56, doi. 10.3390/cryst6050056
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- Article