Found: 13
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Photohydrogenation of Acetophenone Using Coumarin Dye-Sensitized Titanium Dioxide under Visible Light Irradiation.
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- Catalysts (2073-4344), 2015, v. 5, n. 3, p. 1417, doi. 10.3390/catal5031417
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- Article
A Multicomponent Coupling Reaction Induced by Insertion of Arynes into the CO Bond of Formamide.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 29, p. 6638, doi. 10.1002/anie.201102088
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- Article
Three-Component Coupling Reactions of Arynes for the Synthesis of Benzofurans and Coumarins.
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- Molecules, 2014, v. 19, n. 1, p. 863, doi. 10.3390/molecules19010863
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- Article
Oxidative Radical Cyclization–Cyclization Reaction Leading to 1H-Benzo[f ]isoindole Derivatives.
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- Molbank, 2017, v. 2017, n. 1, p. m929, doi. 10.3390/M929
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- Article
2,3,4,9-Tetrahydro-9-(3-hydroxy-1,4-dioxo-1H-dihydro-naphthalen-2-yl)-8-methoxy-3,3-dimethyl-1H-xanthen-1-one.
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- Molbank, 2015, v. 2015, n. 1, p. 1, doi. 10.3390/M841
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- Article
P4-258: Amyloid imaging of a patient with Alzheimer's disease harboring a novel APP mutation (E693Δ)
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- 2008
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- Abstract
P2-054: Pattern of Aβ deposition in familial Alzheimer's disease is not related to mutation type or cognitive status
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- 2008
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- Abstract
O4-06-08: Identification and characterization of a novel APP mutation (E693Δ) in familial Alzheimer's disease
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- 2008
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- Abstract
A Multicomponent Coupling Reaction Induced by Insertion of Arynes into the CO Bond of Formamide.
- Published in:
- Angewandte Chemie, 2011, v. 123, n. 29, p. 6768, doi. 10.1002/ange.201102088
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- Article
Frontispiece: Progress in Enantioselective Radical Cyclizations.
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- Chemistry - A European Journal, 2017, v. 23, n. 26, p. n/a, doi. 10.1002/chem.201782661
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- Article
Progress in Enantioselective Radical Cyclizations.
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- Chemistry - A European Journal, 2017, v. 23, n. 26, p. 6225, doi. 10.1002/chem.201603124
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- Article
A new amyloid β variant favoring oligomerization in Alzheimer's-type dementia.
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- Annals of Neurology, 2008, v. 63, n. 3, p. 377, doi. 10.1002/ana.21321
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- Article
Intramolecular Cyclopropanation of Active Methylene Derivatives Based on FeCl<sub>2</sub> or FeCl<sub>3</sub>‐Promoted Radical‐Polar Crossover Reactions.
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- Chemistry - A European Journal, 2024, v. 30, n. 36, p. 1, doi. 10.1002/chem.202400602
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- Article