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A convenient one-pot approach to the synthesis of novel pyrazino[1,2-a]indoles fused to heterocyclic systems and evaluation of their biological activity as acetylcholinesterase inhibitors.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2021, v. 76, n. 5, p. 303, doi. 10.1515/znb-2020-0205
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The reaction of imidazo[1,5-a]pyridines with ninhydrin revisited.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2020, v. 75, n. 6/7, p. 559, doi. 10.1515/znb-2020-0027
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The reaction of imidazo[1,5-a]pyridines with ninhydrin revisited.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2020, v. 75, n. 6, p. 559, doi. 10.1515/znb-2020-0027
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The reaction of imidazo[1,5-a]pyridines with ninhydrin revisited.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2020, p. 559, doi. 10.1515/znb-2020-0027
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- Article
Facile synthesis of model 2,4-diaryl-1,3,4-thiadiazino[5,6-h]fluoroquinolones.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2019, v. 74, n. 6, p. 507, doi. 10.1515/znb-2019-0023
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Allyl-End-Grafted Carbosilane Dendrimers Based on 1,4-Phenylene Units: Synthesis, Reactivity, Structure, and Bonding Motifs.
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- European Journal of Inorganic Chemistry, 2013, v. 2013, n. 13, p. 2368, doi. 10.1002/ejic.201201428
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A new and convenient synthetic method for 1,2,3,5,6,11b-hexahydroimidazo[1,2-d][1,4]benzoxazepine and its derivatives.
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- ARKIVOC: Online Journal of Organic Chemistry, 2011, p. 277
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- Article
The Nature of Halogen⋅⋅⋅Halogen Synthons: Crystallographic and Theoretical Studies.
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- Chemistry - A European Journal, 2006, v. 12, n. 35, p. 8952, doi. 10.1002/chem.200600523
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- Article
Theoretical and X-ray studies on the cyclization of 1-phenyl-5-(3-aryltriaz-1-en-1-yl)- 1H-pyrazole-4-carbonitriles and 2-amino-3-(3-aryltriaz-1-en-1-yl)maleonitriles: A comparison study.
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- Kuwait Journal of Science, 2022, v. 49, n. 3, p. 1, doi. 10.48129/kjs.14503
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- Article
Bis-heterocycles. Part I: tetrahydro-5,5′- bi(1,2,4-triazin-6-ones).
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2018, v. 73, n. 12, p. 965, doi. 10.1515/znb-2018-0148
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Oxidative coupling of cycloalkanones with 3-(pyridin-2-yl)-1,2,4-triazinone coordinated to Pd(II).
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2018, v. 73, n. 8, p. 583, doi. 10.1515/znb-2018-0077
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A study on the reaction of 3-alkyl(aryl)imidazo[1,5-<italic>a</italic>]pyridines with ninhydrin.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2018, v. 73, n. 6, p. 413, doi. 10.1515/znb-2018-0039
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Heterocycles [h]-fused onto 4-oxoquinoline-3-carboxylic acid. Part XII: synthesis of 5-fluoro-7-oxodihydo[1,3,4]thiadiazino [5,6-h]quinoline-8-carboxylic acid and ester.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2018, v. 73, n. 1, p. 23, doi. 10.1515/znb-2017-0136
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Trimolecular Co-crystals of Ciprofloxacin, p-Coumaric Acid, and Benzoic Acid or Salicylic Acid.
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- Journal of Chemical Crystallography, 2022, v. 52, n. 3, p. 304, doi. 10.1007/s10870-022-00925-5
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4-(9H-Fluoren-9-yl)-4-methylmorpholin-4-ium bromide, C<sub>18</sub>H<sub>20</sub>BrNO.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2021, v. 236, n. 1, p. 179, doi. 10.1515/ncrs-2020-0436
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Crystal structure of 3-(pyrazin-2-ylamino)-2-benzofuran-1(3H)-one, C<sub>12</sub>H<sub>9</sub>N<sub>3</sub>O<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2014, v. 229, n. 4, p. 385, doi. 10.1515/ncrs-2014-0204
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Theoretical study of molecularly imprinted polymers prepared for homatropine methylbromide.
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- Journal of Polymer Research, 2023, v. 30, n. 4, p. 1, doi. 10.1007/s10965-023-03513-z
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Docking, synthesis, and anticancer assessment of novel quinoline-amidrazone hybrids.
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- Pharmacia (0428-0296), 2024, v. 71, n. 1, p. 1, doi. 10.3897/pharmacia.71.e117192
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Thiophene ring-opening reactions VI. Attempted cyclization towards [fused]-tricyclic system involving a thiolate anion and suitably located electrophilic carbon.
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- Zeitschrift für Naturforschung. Section C: A Journal of Biosciences, 2023, v. 78, n. 3/4, p. 133, doi. 10.1515/znc-2022-0080
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