Relevant bibliographies by topics / 1-phenyl-2-thiourea

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Academic literature on the topic '1-phenyl-2-thiourea'

Author: Grafiati
Published: 7 September 2021
Last updated: 29 July 2025

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Journal articles on the topic "1-phenyl-2-thiourea"

1

West, D. X., A. K. Hermetet, L. J. Ackerman, J. Valdés-Martínez, and S. Hernández-Ortega. "3-Phenyl-1-(2-pyridyl)thiourea." Acta Crystallographica Section C Crystal Structure Communications 55, no. 5 (1999): 811–13. http://dx.doi.org/10.1107/s0108270198018083.

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2

Bhattacharjee, Tirtha, Prasanta Gogoi, Vedavati G. Puranik, Rupesh L. Gawade, and Pranjit Barman. "1-Benzoyl-3-[(2-benzylsulfanyl)phenyl]thiourea." Acta Crystallographica Section C Crystal Structure Communications 68, no. 12 (2012): o485—o487. http://dx.doi.org/10.1107/s0108270112045167.

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In the title compound, C21H18N2OS2, a strong intramolecular N—H...O hydrogen bond [N...O = 2.642 (3) Å] between the amide N atom and the benzoyl O atom forms an almost planar six-membered ring in the central part of the molecule. In the crystal, molecules are packed through weak N—H...S interactions. Intra- and intermolecular hydrogen bonds and van der Waals interactions are the stabilizing forces for the crystal structure.
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3

Yue, Huadong, Yifeng Wang, Aibao Xia, Shuping Luo, and Danqian Xu. "1-[3,5-Bis(trifluoromethyl)phenyl]-3-(2-pyridyl)thiourea." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (2008): o858. http://dx.doi.org/10.1107/s1600536808009768.

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4

Xing, Zhi-Yong, and Hai-Tao Zhao. "1-(2-Chlorophenyl)-3-[(phenyl)(4-tolylimino)methyl]thiourea." Acta Crystallographica Section E Structure Reports Online 62, no. 6 (2006): o2268—o2269. http://dx.doi.org/10.1107/s1600536806016916.

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5

Venkatachalam, TK, Elise A. Sudbeck, Chen Mao, and Fatih M. Uckun. "Piperidinylethyl, Phenoxyethyl and Fluoroethyl Bromopyridyl Thiourea Compounds with Potent Anti-HIV Activity." Antiviral Chemistry and Chemotherapy 11, no. 5 (2000): 329–36. http://dx.doi.org/10.1177/095632020001100503.

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Derivatives of piperidinylethyl, phenoxyethyl and fluoroethyl bromopyridyl thioureas were designed and synthesized as non-nucleoside reverse transcriptase inhibitors (NNRTIs) of HIV-1 reverse transcriptase (RT). The anti-HIV activity of these compounds was examined by determining their ability to inhibit the replication of the HIV-1 strain HTLVIIIB in human peripheral blood mononuclear cells. The unsubstituted parent pyridyl thiourea compound N-[2-(1-piperidine)ethyl]-N′-[2-(pyridyl)] thiourea (1) exhibited no anti-HIV activity, even at 100 μM. However, the thiourea derivatives that contain a
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6

Sheena Mary, Y., V. V. Aswathy, C. Yohannan Panicker, et al. "Spectroscopic, single crystal XRD structure, DFT and molecular dynamics investigation of 1-(3-chloro-4-fluorophenyl)-3-[3-(trifluoromethyl)phenyl]thiourea." RSC Advances 6, no. 113 (2016): 111997–2015. http://dx.doi.org/10.1039/c6ra21396k.

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7

Ferrari, Marisa Belicchi, Giovanna Gasparri Fava, Corrado Pelizzi, and Pieralberto Tarasconi. "Synthesis and structural characterization of chloro-(triphenylphosphine)-[1-phenyl-3-(2-pyridyl)-2-thiourea]Cu(I) and chloro-bis[1-[phenyl-3-(2-pyridyl)-2-thiourea]-Cu(I)." Inorganica Chimica Acta 97, no. 1 (1985): 99–109. http://dx.doi.org/10.1016/s0020-1693(00)87996-7.

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8

Narule, Meghasham, Jyotsna Meshram, B. Santhakumari, and A. Shanware. "Synthesis of 2-[4-(10H-Substituted Phenothiazine-3-yl)-6-Pyrimidin-2-Phenylthiol/ol/amine/thiol] Pyrroles." E-Journal of Chemistry 4, no. 1 (2007): 53–59. http://dx.doi.org/10.1155/2007/572543.

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2-[4-Hydroxy benz-1(propene-1-one)]Pyrrole II on treatment with phenyl thiourea, guanidine carbonate, urea and thiourea in alcoholic KOH yielded compounds III, IV, V, VI which on treatment with different aryl anilines gave compounds VII, VIII, IX, X which under goes cyclisation with sulphur and iodine to give 2-[4-(10H-substituted phenothiazine-3-yl)-6-pyrimidin-2-phenylthiol/-ol/-amine/-thiol] pyrrole XI(a-j), XII(a-j), XIII(a-j) and XIV(a-j) respectively. The structural products were characterized by elemental analysis and spectral data.
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9

V, Mujalda, S. Tiwari, V. Sharma, P. Saxena, and M. Shrivastava. "Synthesis of 3-chloro-4- (2-hydroxy-5-(substituted phenyl (diazyl)-N-[(4-oxo-2-phenylquinazoline 3(4H)-yl)]-2-oxoazetidine-1-carbothiamide Analogs as Potential Antimicrobial Agents." International Journal of Drug Design and Discovery 3, no. 2 (2025): 798–802. https://doi.org/10.37285/ijddd.3.2.8.

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Some new series of 3-chloro-4-(2-hydroxy-5-(substituted phenyl (diazyl)-N-[(4-oxo -2-phenylquinazoline 3(4H)-yl)]-2-oxoazetidine-1-carbothiamide have been synthesized by the reaction of 1-[2-hydroxyl–5–(substituted phenyl)diazyl benzylidene-3-(4-oxo-2-phenylquinazolin-3(4H)-yl) thiourea with chloroacetyl chloride and triethyl amine in 1,4 dioxane. The structure of synthesized compounds is confirmed by IR, NMR & Mass spectral studies. The antimicrobial activities of the synthesized compounds were evaluated by screening on different human pathogens using the disc diffusion assay.
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10

Rosiak, Damian, Andrzej Okuniewski, and Jarosław Chojnacki. "The influence of the type of halogen substituent and its position on the molecular conformation, intermolecular interactions and crystal packing for a series of 1-benzoyl-3-(halogenophenyl)thioureas." Acta Crystallographica Section C Structural Chemistry 77, no. 1 (2021): 11–19. http://dx.doi.org/10.1107/s2053229620015594.

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By the reaction of benzoyl chloride, potassium isothiocyanate and the appropriate halogenoaniline, i.e. 2/3/4-(bromo/iodo)aniline, we have obtained five new 1-benzoyl-3-(halogenophenyl)thioureas, namely, 1-benzoyl-3-(2-bromophenyl)thiourea and 1-benzoyl-3-(3-bromophenyl)thiourea, C14H11BrN2OS, and 1-benzoyl-3-(2-iodophenyl)thiourea, 1-benzoyl-3-(3-iodophenyl)thiourea and 1-benzoyl-3-(4-iodophenyl)thiourea, C14H11IN2OS. Structural and conformational features of the compounds have been analyzed using X-ray diffraction and theoretical calculations. The novel compounds were characterized by solid-
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Dissertations / Theses on the topic "1-phenyl-2-thiourea"

1

Fernandes, Sónia Rafaela Beleza. "Detection and characterization of phenoloxidasse in Chironomus riparius." Master's thesis, Universidade de Aveiro, 2018. http://hdl.handle.net/10773/22027.

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Mestrado em Biologia Molecular e Celular<br>Insects are frequently exposed to a large variety of microbes, microorganisms and parasites which requires an effective immune system of defence against infections. However, insects lack an adaptive immune system, so they have developed other highly effective systems of host defence, such as innate immune reactions. These innate immune reactions refer to the first-line of defence of hosts against bacterial, fungal, and viral pathogens. Research on invertebrate model systems have been increasing and becoming very important in ecological immunology res
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