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Relevant bibliographies by topics / P-tolyl compounds

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Academic literature on the topic 'P-tolyl compounds'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "P-tolyl compounds"

1

Janam Singh, Ram, and Dharmendra Kumar Singh. "Syntheses of Some 3,5-Diaryl-4H-1,2,4-triazole Derivatives and their Antifungal Activity." E-Journal of Chemistry 6, s1 (2009): S219—S224. http://dx.doi.org/10.1155/2009/925964.

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Syntheses of a series of 3, 5-diaryl-4H-1, 2, 4-triazole derivatives are described. In this present work, 4-amino-3-phenyl-5-p-tolyl-4H-1,2,4-triazole(1) was converted toN,N’-bis[3-phenyl-5-p-tolyl-4H-1,2,4-triazolyl]-1,4-xylenediimine(2) and 3-Phenyl-5-p-tolyl-4-[4-methyl benzylidenamino]-4H-1,2,4-triazole (3) in good yields by treatment with aldehydes OHC-C6H4-CHO and Ar-CHO respectively. The compoundsN,N’-bis[3-phenyl-5-p-tolyl-4H-1,2,4-triazolyl]-1,4-xylenediimine (2) and 3-phenyl-5-p-tolyl-4-[4-methyl benzylidenamino]-4H-1,2,4-triazole (3) were reduced with NaBH4to afford the correspondin

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2

Gonca, Ergün, Ümmü Gülsüm Baklaci, and Hatice Akin Dinçer. "Seco-porphyrazines with eight (p-tolyl) and (o-tolyl) units." Journal of Porphyrins and Phthalocyanines 12, no. 02 (2008): 116–22. http://dx.doi.org/10.1142/s1088424608000157.

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Magnesium porphyrazinates substituted with eight (p-tolyl) and (o-tolyl) units on the peripheral positions have been synthesized for the first time by cyclotetramerization of 1,2-bis(p-tolyl)maleonitrile and 1,2-bis(o-tolyl)maleonitrile in the presence of magnesium butanolate. Their demetalation by the treatment with trifluoroacetic acid resulted in partially oxidized products, namely, octakis(p-tolyl)-2-seco-porphyrazine-2,3-dione and octakis(o-tolyl)-2-seco-porphyrazine-2,3-dione. Further reactions of these products with copper(II) acetate, zinc(II) acetate and cobalt(II) acetate have led to

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3

Kimura, Tsutomu, Koto Sekiguchi, Akane Ando, and Aki Imafuji. "Fritsch–Buttenberg–Wiechell rearrangement of magnesium alkylidene carbenoids leading to the formation of alkynes." Beilstein Journal of Organic Chemistry 17 (May 28, 2021): 1352–59. http://dx.doi.org/10.3762/bjoc.17.94.

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A series of 1-heteroatom-substituted vinyl p-tolyl sulfoxides were prepared and treated with organometallic reagents to evaluate which combination of sulfoxides and organometallic reagents yielded alkynes the most efficiently. The use of 1-chlorovinyl p-tolyl sulfoxide and isopropylmagnesium chloride was optimal for this purpose. A variety of 1-chlorovinyl p-tolyl sulfoxides were prepared from carbonyl compounds and chloromethyl p-tolyl sulfoxide and were converted into alkynes via the sulfoxide/magnesium exchange reaction and subsequent Fritsch–Buttenberg–Wiechell (FBW) rearrangement of the r

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4

Schumann, Herbert, and Klaudia Sühring. "Di-, Hexa- und Deca-substituierte Decaphenylferrocene / Di-, Hexa- and Deca-Substituted Decaphenylferrocenes." Zeitschrift für Naturforschung B 60, no. 4 (2005): 383–88. http://dx.doi.org/10.1515/znb-2005-0404.

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5-Bromo-1,2,3,4-tetraphenyl-5-p-tolyl-1,3-cyclopentadiene (1a), 5-Bromo-1,4-di-phenyl-2,3,5- tri-p-tolyl-1,3-cyclopentadiene (1b), 5-Bromo-1,2,3,4,5-penta-p-tolyl-1,3-cyclopentadiene (1c), 5- Bromo-1,2,3,4-tetraphenyl-5-p-bromophenyl-1,3-cyclopentadiene (1d), and 5-Bromo-1,2,3,4-tetraphenyl- 5-p-anisyl-1,3-cyclopentadiene (1e) react with ironpentacarbonyl in m-xylene to yield the corresponding ferrocenes 2a - 2e. In the course of the purification procedure, reactions with HCl and the solvent m-xylene are observed which yield the mixed ionic sandwich complexes [(C5Ph4C6H4Me)Fe(C6H4Me2)]+Cl− (3a

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5

Făgădar-Cosma, Eugenia, Maria Laichici, Gheorghe Făgădar-Cosma, and Dana Vlascici. "Synthesis, characterization and correlative biological effects in wheat of a benzoxaza- and a diaza-phosphorus(V) heterocycles." Journal of the Serbian Chemical Society 71, no. 10 (2006): 1031–38. http://dx.doi.org/10.2298/jsc0610031f.

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Dichloro-p-tolylphosphine, involved in a Mannich type reaction, together with o-aminophenol or 1,2- diaminopropane and acetone generated two phosphorin- 2-oxide ring compounds, namely: hexahydro-3,3,5-trimethyl-2-p-tolyl-1,4,2-diazaphosphorine- 2-oxide and 3,4-dihydro-3,3-dimethyl-2-p-tolyl-2H-1,4,2-benzoxaza- phosphorine-2-oxide. The two compounds were fully characterized by MS, IR, UV, 1H-NMR, and gas chromatography. Anothermain objective of the present study was to examine to what extent the treatments with different concentrations of the above-mentioned diaza- and benzoxaza-compounds affec

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6

Variya, Hiren H., Vikram Panchal, Falguni G. Bhabhor, and G. R. Patel. "Synthesis and Characterization of Biologically Potent Chalcone Bearing 1,3,4-Oxadiazole Linkage." International Letters of Chemistry, Physics and Astronomy 61 (November 3, 2015): 77–83. http://dx.doi.org/10.56431/p-x4q61z.

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In this article, we have described to design and synthesized a series of substituted chalcone based 1,3,4-oxadiazole derivatives. Titled compounds (E)-S-(-5-phenyl-1,3,4-oxadiazol-2-yl) 2-(4-(3-(5-methyl-3oxo-2(p-tolyl)-2,3-dihydro-1H-pyrazol-4-yl)-3-oxoprop-1-en-1-yl) phenoxy) etanethioate (III1-6) were synthesized using of derivatives of S-(-5-phenyl-1,3,4 oxadiazole-2-yl)2-chloroethaethioate (I1-6) were reacted with (E)-4-(3-(4-hydroxyphenyl) acryloyl)-5-methyl-2(p-tolyl)-1H-pyrazol-3(2H)-one (II) in presence of K2CO3 in DMF as a solvent. The synthesized compounds were evaluated for their a

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Variya, Hiren H., Vikram Panchal, Falguni G. Bhabhor, and G. R. Patel. "Synthesis and Characterization of Biologically Potent Chalcone Bearing 1,3,4-Oxadiazole Linkage." International Letters of Chemistry, Physics and Astronomy 61 (November 2015): 77–83. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.61.77.

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In this article, we have described to design and synthesized a series of substituted chalcone based 1,3,4-oxadiazole derivatives. Titled compounds (E)-S-(-5-phenyl-1,3,4-oxadiazol-2-yl) 2-(4-(3-(5-methyl-3oxo-2(p-tolyl)-2,3-dihydro-1H-pyrazol-4-yl)-3-oxoprop-1-en-1-yl) phenoxy) etanethioate (III1-6) were synthesized using of derivatives of S-(-5-phenyl-1,3,4 oxadiazole-2-yl)2-chloroethaethioate (I1-6) were reacted with (E)-4-(3-(4-hydroxyphenyl) acryloyl)-5-methyl-2(p-tolyl)-1H-pyrazol-3(2H)-one (II) in presence of K2CO3 in DMF as a solvent. The synthesized compounds were evaluated for their a

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8

Pokotylo, Ihor O., Pavlo V. Zadorozhnii, Vadym V. Kiselev, Oxana V. Okhtina, and Aleksandr V. Kharchenko. "Some New Heterocyclisations Based on N-(2,2-dichloro-1-isothiocyanatoethyl)benzamide Derivatives." Acta Chemica Iasi 27, no. 1 (2019): 65–72. http://dx.doi.org/10.2478/achi-2019-0005.

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Abstract Based on the readily available N-(2,2-dichloro-1-(2-(4-methylbenzoyl)-hydrazine-1-carbothioamido)ethyl)benzamide, the corresponding N-(2,2-dichloro-1-((5-(p-tolyl)-1,3,4-oxadiazol-2-yl)amino)ethyl)benzamide and 5-(p-tolyl)-1,3,4-thiadiazol-2-amine were obtained. The products were received in acceptable yields and were isolated from the reaction mixture without any particular difficulty. The structure of the compounds obtained was confirmed by 1H, 13C NMR spectroscopy and mass spectrometry data.

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9

Nguyen, Cong Tien, Ha Manh Bui, and Duyen Hoang My Nguyen. "Synthesis of 2-(2-(4-Phenyl-2,3-Dihydrobenzo[B][1,4]Thiazepin-2-YL) Phenoxy)-N-(P-Tolyl)Acetamide." Acta Chemica Iasi 26, no. 1 (2018): 13–20. http://dx.doi.org/10.2478/achi-2018-0002.

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Abstract The A new benzothiazepine’s derivative names N-(p-tolyl)-2-(2-(4-phenyl-2,3-dihydrobenzo[b][1,4]thiazepin-2-yl)phenoxy)acetamide was synthesized by reaction of o-aminothiophenol and N-(p-tolyl)-2-(2-(3-oxo-3-phenylprop-1-en-1-yl)phenoxy)acetamide, which was prepared from salicylaldehyde and acetophenone through (E)-3-(2-hydroxyphenyl)-1-phenylprop-2-en-1-one. The structures of the compounds were determined by IR, 1H-NMR, 13C-NMR and HR-MS spectral data.

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10

Boukthir, Mouna, Zribi Fethi, Iman Halloum, Laurent Kremer, and Fakher Chabchoub. "Synthesis and Antitubercular Evaluation of Some Novel 1,2,3,6-tetrahydropyrimidine-5-carbonitrile." JOURNAL OF ADVANCES IN CHEMISTRY 9, no. 3 (2013): 2072–77. http://dx.doi.org/10.24297/jac.v9i3.1014.

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In an attempt to find a new class of antitubercular agents, a series of 1,2,3,6-tetrahydropyrimidine-5-carbonitrile were prepared via the reaction of ethyl N-ethoxycarbonylbenzimidate 2a-b with cyanoacetanilide derivatives 1a-c. These compounds were screened for their antitubercular activity against M. tuberculosis. Several analogues, such as 2,6-dioxo-1-phenyl-4-p-tolyl-1,2,3,6-tetrahydropyrimidine-5-carbonitrile 3a, 1-benzyl-2, 6-dioxo-4-p-tolyl-1,2,3,6-tetrahydropyrimidine-5-carbonitrile 3c and 1-benzyl-2, 6-dioxo-4-phenyl-1,2,3,6-tetrahydropyrimidine-5-carbonitrile 3d exhibited a potent an

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Dissertations / Theses on the topic "P-tolyl compounds"

1

Schmitt, Gérard. "Réactions de l'hydrofluoroborate d'un composé de Reissert sur divers alcenes : Compétition entre cycloaddition dipolaire-1,3 et cycloaddition de Diels-Alder." Besançon, 1987. http://www.theses.fr/1987BESA2041.

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Book chapters on the topic "P-tolyl compounds"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadium(III) complex of salicylaldehyde-4-p-tolyl-thiosemicarbazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_415.

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2

Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadium(III) complex of 5-bromo-salicylaldehyde-p-tolyl-thiosemicarbazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_416.

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3

Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadium(III) complex of 5-chloro-salicylaldehyde-p-tolyl-thiosemicarbazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_417.

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4

Pardasani, R. T., and P. Pardasani. "Magnetic properties of (μ-oxo)bis[meso-tetrakis(p-tolyl-porphyrinato)iron(III)." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_45.

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5

Pardasani, R. T., and P. Pardasani. "Magnetic properties of mononuclear copper(II) chloro complex with N-salicylidene-p-tolyl-hydrazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_285.

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6

Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) chloro complex with N-salicylidene-p-tolyl-hydrazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_289.

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7

Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) aqua complex with N-salicylidene-p-tolyl-hydrazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_292.

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8

Pardasani, R. T., and P. Pardasani. "Magnetic properties of diphenylosmium(V) complex with 5, 10, 15, 20-tetra(p-tolyl)porphyrin." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_270.

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9

Pardasani, R. T., and P. Pardasani. "Magnetic properties of di-μ-hydroxobridged dicopper(II) complex with N-salicylidene-p-tolyl-hydrazine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_282.

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10

Pardasani, R. T., and P. Pardasani. "Magnetic properties of osmium(IV) chloride complex with 5, 10, 15, 20-tetra(p-tolyl)porphyrin." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_268.

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