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Journal articles on the topic 'N-benzyl anilines'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Neeraj, Rani, R. Sharma J., K. Kaul V., and R. Manrao M. "Secondary amines : Synthesis and effect of length of spacer linking two phenyl rings on biological activity." Journal of Indian Chemical Society Vol. 85, Oct 2008 (2008): 1041–44. https://doi.org/10.5281/zenodo.5820670.

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Department of Chemistry, Department of Plant Pathology, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>Manuscript received 7 January 2008, revised 30 June 2008, accepted 16 July 2008</em> N-Benzyl benzylamines (1a-11a) and N-benzyl anilines (1b-11b) were synthesized by sodium borohydride reduction of aldimines of benzylamine and aniline respectively. The products were characterized on the basis of elemental analysis and spectral studies and screened for antifungal potential against four fungi and evaluated for nematicidal activity against two nematodes. The former compound

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2

Li, Lu, Na Li, Xiao-Tian Mo, Ming-Wei Yuan, Lin Jiang, and Ming-Long Yuan. "Synthesis of 2-benzyl N-substituted anilines via imine condensation–isoaromatization of (E)-2-arylidene-3-cyclohexenones and primary amines." Beilstein Journal of Organic Chemistry 20 (July 2, 2024): 1468–75. http://dx.doi.org/10.3762/bjoc.20.130.

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A catalyst- and additive-free synthesis of 2-benzyl N-substituted anilines from (E)-2-arylidene-3-cyclohexenones and primary amines has been reported. The reaction proceeds smoothly through a sequential imine condensation–isoaromatization pathway, affording a series of synthetically useful aniline derivatives in acceptable to high yields. Mild reaction conditions, no requirement of metal catalysts, operational simplicity and the potential for scale-up production are some of the highlighted advantages of this transformation.

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3

Pati, Hari, Paul Weisbruch, Adrienne Lemon, and Moses Lee. "Synthesis of N‐Benzylated Anilines from the Reaction of Anilines and Benzyl Chloroformate." Synthetic Communications 34, no. 5 (2004): 933–40. http://dx.doi.org/10.1081/scc-120028366.

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4

Goyal, Vishakha, Naina Sarki, Mukesh Kumar Poddar, et al. "Biorenewable carbon-supported Ru catalyst for N-alkylation of amines with alcohols and selective hydrogenation of nitroarenes." New Journal of Chemistry 45, no. 32 (2021): 14687–94. http://dx.doi.org/10.1039/d1nj01654g.

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A renewable carbon-supported Ru catalyst (Ru/PNC-700) facilely prepared via simple impregnation followed by the pyrolysis process for N-alkylation of anilines with benzyl alcohol and chemoselective hydrogenation of nitroarenes.

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5

Qiao, Mengjun, Jinli Zhang, Ling Chen та ін. "Transition metal-free α-Csp3–H oxidative sulfuration of benzyl thiosulfates with anilines to form N-aryl thioamides". Organic & Biomolecular Chemistry 17, № 15 (2019): 3790–96. http://dx.doi.org/10.1039/c9ob00336c.

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6

Dubey, Pooja, Sonu Gupta та Ajai K. Singh. "Base free N-alkylation of anilines with ArCH2OH and transfer hydrogenation of aldehydes/ketones catalyzed by the complexes of η5-Cp*Ir(iii) with chalcogenated Schiff bases of anthracene-9-carbaldehyde". Dalton Transactions 47, № 11 (2018): 3764–74. http://dx.doi.org/10.1039/c7dt04326k.

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7

Štěpnička, Petr, Tomáš Baše, Ivana Císařová, Jiří Kubišta, Štěpán Vyskočil, and Martin Štícha. "Synthesis and Catalytic Activity of Spaced Ferrocene Oxazolines." Collection of Czechoslovak Chemical Communications 68, no. 7 (2003): 1206–32. http://dx.doi.org/10.1135/cccc20031206.

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Chiral 2-[{N-aryl-N-(ferrocenylmethyl)amino}methyl]-4-(1-methylethyl)-4,5-dihydroxazoles with various substituents at the aryl ring were prepared by alkylation of N-(ferrocenylmethyl)anilines, FcCH2NHC6H4R (Fc = ferrocenyl), with (S)-2-(chloromethyl)-4-(1-methylethyl)-4,5-dihydrooxazole. The oxazoles, substituted anilines, and the precursors of the latter, the respective Schiff bases FcCH=NC6H4R, were characterized by standard methods and further studied by mass spectrometry. The oxazoles were further tested as chiral auxiliaries in the addition of diethylzinc to benzaldehyde but showed only n

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8

Gorrod, John W., та Nigel J. Gooderham. "Improved Preparation of α,N-Diphenylnitrones andN-Benzyl-N-Phenylhydroxylamines by direct Oxidation of Secondary Anilines". Archiv der Pharmazie 319, № 3 (1986): 261–65. http://dx.doi.org/10.1002/ardp.19863190313.

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9

Al Mamari, Hamad H. "Ir-Catalyzed ortho-C-H Borylation of Aromatic C(sp2)-H Bonds of Carbocyclic Compounds Assisted by N-Bearing Directing Groups." Reactions 5, no. 2 (2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.

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C-H borylation is a powerful strategy for the construction of C-B bonds due to the synthetic versatility of C-B bonds. Various transition metals affect the powerful functionalization of C-H bonds, of which Ir is the most common. Substrate-directed methods have enabled directed Ir-catalyzed C-H borylation at the ortho position. Amongst the powerful directing groups in Ir-catalyzed C-H borylation are N-containing carbocyclic systems. This review covers substrate-directed Ir-catalyzed ortho-C-H borylation of aromatic C(sp2)-H bonds in N-containing carbocyclic compounds, such as anilines, amides,

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10

Laha, Joydev K., Pankaj Gupta, and Amitava Hazra. "Sulfate radical anion-induced benzylic oxidation of N-(arylsulfonyl)benzylamines to N-arylsulfonylimines." Beilstein Journal of Organic Chemistry 19 (June 5, 2023): 771–77. http://dx.doi.org/10.3762/bjoc.19.57.

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A mild, operationally convenient, and practical method for the synthesis of synthetically useful N-arylsulfonylimines from N-(arylsulfonyl)benzylamines using K2S2O8 in the presence of pyridine as a base is reported herein. In addition, a “one-pot” tandem synthesis of pharmaceutically relevant N-heterocycles by the reaction of N-arylsulfonylimines, generated in situ with ortho-substituted anilines is also reported. The key features of the protocol include the use of a green oxidant, a short reaction time (30 min), chromatography-free isolation, scalability, and economical, delivering N-arylsulf

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11

Saidulu, G., R. Arun Kumar, and K. Rajender Reddy. "Iron-catalyzed C–N bond formation via oxidative Csp3–H bond functionalization adjacent to nitrogen in amides and anilines: Synthesis of N-alkyl and N-benzyl azoles." Tetrahedron Letters 56, no. 28 (2015): 4200–4203. http://dx.doi.org/10.1016/j.tetlet.2015.05.048.

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12

Dey, Raghunath, and Prabal Banerjee. "Metal‐Free Ring Opening Cyclization of Cyclopropane Carbaldehydes and N ‐Benzyl Anilines: An Eco‐Friendly Access to Functionalized Benzo[ b ]azepine Derivatives." Advanced Synthesis & Catalysis 361, no. 12 (2019): 2849–54. http://dx.doi.org/10.1002/adsc.201801714.

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13

Saidulu, G., R. Arun Kumar, and K. Rajender Reddy. "ChemInform Abstract: Iron-Catalyzed C-N Bond Formation via Oxidative C(sp3)-H Bond Functionalization Adjacent to Nitrogen in Amides and Anilines: Synthesis of N-Alkyl and N-Benzyl Azoles." ChemInform 46, no. 41 (2015): no. http://dx.doi.org/10.1002/chin.201541087.

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14

Zhang, Hongming, Jiahe Zhuang, Xiangrui Feng, and Ben Ma. "Co0.6Ni0.4S2/rGO Photocatalyst for One-Pot Synthesis of Imines from Nitroaromatics and Aromatic Alcohols by Transfer Hydrogenation." Coatings 12, no. 12 (2022): 1799. http://dx.doi.org/10.3390/coatings12121799.

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Co0.6Ni0.4S2/rGO catalysts exhibit excellent photocatalytic performance for one-step synthesis of N-benzylideneaniline from nitrobenzene and benzyl alcohol by transfer hydrogenation, and the selectivity and yield of N-benzylideneaniline can reach as high as 93% and 77.2%, respectively. The reaction process for the synthesis of imines can be divided into two steps: benzyl alcohol is oxidized to benzaldehyde, while nitrobenzene is reduced to aniline; benzaldehyde and aniline are condensed to form imines. Under visible light irradiation, photo-induced electrons in Co0.6Ni0.4S2/rGO photocatalyst p

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15

Jílek, Jiří, Miroslav Rajšner, Vladimír Valenta, et al. "Synthesis of piperidine derivatives as potential analgetic agents." Collection of Czechoslovak Chemical Communications 55, no. 7 (1990): 1828–53. http://dx.doi.org/10.1135/cccc19901828.

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Reaction of N-(1-(2-phenylethyl)-4-piperidinyl)propionanilide (I) with phosphorus pentasulfide gave the thioamide VI. Acylation of N-(1-(2-phenylethyl)-4-piperidinyl)aniline with 2-(methoxy)acetic and 2-(methylthio)acetic anhydrides afforded the amides II and III. Treatment of 4-anilino-1-benzylpiperidine-4-methanol with thionyl chloride gave the spirocyclic sulfurous acid ester amide XIV. Reduction of the hydrochloride of ethyl 3-(1-ethoxycarbonyl-4-phenylimino-3-piperidinyl)propionate (XXII) with sodium cyanoborohydride gave the perhydro-1,6-naphthyridine derivative XIX, a model compound in

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16

Liu, Huihui, Gaik Khuan Chuah, and Stephan Jaenicke. "Alumina-entrapped Ag catalyzed nitro compounds coupled with alcohols using borrowing hydrogen methodology." Physical Chemistry Chemical Physics 17, no. 22 (2015): 15012–18. http://dx.doi.org/10.1039/c5cp00330j.

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Time-yield plots for the N-alkylation of nitroarenes with benzyl alcohol in the presence of Ag/Al<sub>2</sub>O<sub>3</sub>. (■) conversion; (⋄) N-phenylbenzylamine 3; (▲) N-benzylideneaniline 4; (□) azobenzene 5; and (+) aniline 6.

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17

Ciber, Luka, Helena Brodnik, Franc Požgan, Jurij Svete, Bogdan Štefane, and Uroš Grošelj. "Synthesis of N1-(3,5-Bis(trifluoromethyl)benzyl)benzene-1,2-diamine and N,N-Bis(2-nitrophenyl)-3,5-bis(trifluoromethyl)aniline." Molbank 2023, no. 3 (2023): M1718. http://dx.doi.org/10.3390/m1718.

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A monosubstituted benzene-1,2-diamine building block, N1-(3,5-bis(trifluoromethyl)benzyl)benzene-1,2-diamine, was prepared in two steps from commercially available 3,5-bis(trifluoromethyl)benzylamine and 1-fluoro-2-nitrobenzene, while the use of 3,5-bis(trifluoromethyl)aniline as the starting amine gave a triarylamine, N,N-bis(2-nitrophenyl)-3,5-bis(trifluoromethyl)aniline. The structures of the newly synthesized compounds were fully characterized.

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18

Zhang, Zhi Ming, Shi Qian Wei, and Li Hua Han. "Study of Synthesis and Properties on Poly L-Glutamate Initiated by Aniline." Advanced Materials Research 284-286 (July 2011): 2110–13. http://dx.doi.org/10.4028/www.scientific.net/amr.284-286.2110.

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With L-glutamic acid as raw materials, N-carboxy-L-glutamic acid-benzyl-anhydride (BLG-NCA) was synthesized by triphosgene. With aniline as the initiator in the anhydrous dichloromethane, ring-opening polymerization of BLG-NCA was initiated, poly-l-glutamic acid benzyl ester was obtained. The amount of initiators, Molar ratio of monomer/initiators, reaction temperature and reaction time to the effect of poly-l-glutamic acid benzyl ester in the ring-opening polymerization of BLG-NCA were studied. Through infrared spectroscopy, gel permeation chromatography (GPC) analysis and characteristic visc

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19

Dmitrii, A. Pisanenko, E. Klimko Yurii, Dubskaja Sofia, and L. Voljanskii Yurii. "Synthesis and Antimicrobial Activity of Some 3-(N-Arylcarboxamido)-N-benzyl halides." Chemistry Research Journal 2, no. 5 (2017): 238–41. https://doi.org/10.5281/zenodo.13951595.

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Some 3-(N-arylcarboxamido)-N-benzylchlorides, bromides and iodides were synthesized by quaternization of N-arylnicotinamides with benzyl halides. N-Arylnicotinamides were obtained by acylation of aniline, 1- and 2-naphthylamines with chloride of nicotinic acid. The synthesized salts were employed in antimicrobial tests against both Gram- negative, Gram-positive bacteria and fungus using the microdilution method. Antimicrobial tests indicated that all salts have reasonable activity but the salts containing iodine anions are more active than others in the series against majority of tested bacter

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20

Journal, Baghdad Science. "Synthesis , characterization and biological activity study of N-substituted sulfonamido maleimides substituted with different heterocycles." Baghdad Science Journal 7, no. 1 (2010): 641–53. http://dx.doi.org/10.21123/bsj.7.1.641-653.

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Eighteen new cyclic imides (maleimides) conncted to benzothiazole moiety through sulfonamide group were synthesized via multistep synthesis.The first step involved preparation of two maleamic acids N-phenylmaleamic acid and N-benzylmaleamic acid via reaction of maleic anhydride with aniline or benzyl amine.Dehydration of the prepared amic acids by treatment with acetic anhydride and anhydrous sodium acetate in the second step afforded N-phenylmaleimide and N- benzyl maleimide which in turn were treated with chlorosulfonic acid in the third step to afford 4-(N-maleimidyl) phenyl sulfonyl chlori

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21

Zhang, Xusheng, Min Wang, Pinhua Li, and Lei Wang. "n-Bu4NI/TBHP-catalyzed direct amination of allylic and benzylic C(sp3)–H with anilines under metal-free conditions." Chem. Commun. 50, no. 59 (2014): 8006–9. http://dx.doi.org/10.1039/c4cc01189a.

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22

Shainova, Roza S., Tiruhi A. Gomktsyan, Armen V. Karapetyan, and Aleksandr P. Yengoyan. "Synthesis and biological evaluation of 3-O-substituted 1-benzyl-6-oxo-1,6-dihydropyridazine derivatives." Journal of Chemical Research 43, no. 9-10 (2019): 352–58. http://dx.doi.org/10.1177/1747519819866402.

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On the basis of 2-benzyl-6-hydroxypyridazin-3(2 H)-one, a series of its novel O-substituted (including 6-(1,3,5-triazin-2-yl)oxy) derivatives is prepared. It is proven that the substitution reactions in the initial compound occur mainly at the oxygen atom of the hydroxy group. On the basis of the obtained oxy-aceto(propane)hydrazides, the corresponding azides and anilides are synthesized. A series of 2-[(1-benzyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy]- N′-(substituted benzylidene)aceto(propane)hydrazides is obtained via the reaction of various aromatic aldehydes with the same hydrazides. Heteroc

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23

Hu, Sheng-Li, Yi-Tao Li, and Li-Ping Cao. "N-[(E)-4-Pyridylmethylene]-4-[(E)-4-(4-pyridylmethyleneamino)benzyl]aniline tetrahydrate." Acta Crystallographica Section E Structure Reports Online 64, no. 1 (2007): o115. http://dx.doi.org/10.1107/s1600536807063179.

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24

Mhadmhan, Marquez-Medina, Romero, Reubroycharoen, and Luque. "Fe-Containing MOFs as Seeds for the Preparation of Highly Active Fe/Al-SBA-15 Catalysts in the NAlkylation of Aniline." Molecules 24, no. 15 (2019): 2695. http://dx.doi.org/10.3390/molecules24152695.

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We have successfully incorporated iron species into mesoporous aluminosilicates (AlSBA15) using a simple mechanochemical milling method. The catalysts were characterized by nitrogen physisorption, inductively coupled plasma mass spectrometry (ICP-MS), pyridine (PY) and 2,6-dimethylpyridine (DMPY) pulse chromatography titration, powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX). The catalysts were tested in the N-alkylation reaction of aniline with benzyl alcohol for imine production. Accor

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25

Krchňák, Viktor, Jennifer Smith, and Josef Vágner. "Solid-Phase Traceless Synthesis of Selected Nitrogen-Containing Heterocyclic Compounds. The Encore Technique for Directed Sorting of Modular Solid Support." Collection of Czechoslovak Chemical Communications 66, no. 7 (2001): 1078–106. http://dx.doi.org/10.1135/cccc20011078.

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The acid lability of electron-rich N-benzylanilines has been exploited in a linker for the traceless solid-phase synthesis of benzimidazoles, 2-aminobenzimidazoles, quinoxalinones and tetrahydroquinoxalines. The target compound precursors were assembled on a solid-phase support derivatized with either a benzylamine or a benzhydrylamine linker. Exposure to an acidic reagent caused cleavage of the C(benzyl)-N(aniline) bond, releasing the product with only a hydrogen atom on the descending nitrogen. The Encore technique for directed sorting on SynPhase Lanterns has been developed and applied to c

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26

Yazdanbakhsh, M. R., A. Mohammadi, E. Mohajerani, et al. "Novel azo disperse dyes derived from N-benzyl–N-ethyl–aniline: Synthesis, solvatochromic and optical properties." Journal of Molecular Liquids 151, no. 2-3 (2010): 107–12. http://dx.doi.org/10.1016/j.molliq.2009.11.010.

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27

Chen, Zheng-Bo, Jun Wu, Pei-Zhi Zhang, Pei-Min Zhang, and Jing Lv. "4-(2-Chloro-4-nitrophenoxy)-N-[2-(4,6-dimethoxypyrimidin-2-yloxy)benzyl]aniline." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): o1671—o1672. http://dx.doi.org/10.1107/s1600536806010671.

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In the title molecule, C25H21Cl1N4O6, all bond lengths and angles show normal values. Weak intermolecular C—H...Cl hydrogen bonds link the molecules into chains extending along the crystallographic c axis. The crystal packing is further stabilized by van der Waals forces.

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28

Hikawa, Hidemasa, Mika Matsumoto, Sayoko Tawara, Shoko Kikkawa, and Isao Azumaya. "Gold(III)/Sodium Diphenylphosphinobenzene-3-sulfonate (TPPMS) Catalyzed Dehydrative N-Benzylation of Electron-Deficient Anilines in Water." Synthesis 51, no. 13 (2019): 2729–36. http://dx.doi.org/10.1055/s-0037-1611519.

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A strategy for the dehydrative N-benzylation of electron-deficient anilines in water has been developed. The gold(III)/sodium diphenylphosphinobenzene-3-sulfonate (TPPMS) catalyst is highly effective as a Lewis acid for the activation of alcohols and tolerates aerobic conditions. A Hammett study in the reaction of para-substituted benzhydryl alcohols shows negative σ values, indicating a build-up of cationic charge during the rate-determining sp3 C–O bond-cleavage step. The inverse kinetic solvent isotope effect (KSIE = 0.6) is consistent with a specific acid catalysis mechanism. This simple p

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29

Putro, Wahyu S., Takayoshi Hara, Nobuyuki Ichikuni, and Shogo Shimazu. "One-pot synthesis of aniline N-alkylation from benzyl alcohol over Cu-Fe catalyst." Applied Catalysis A: General 602 (July 2020): 117519. http://dx.doi.org/10.1016/j.apcata.2020.117519.

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30

Yue, Yongli, Yuanhua Wang, and Wenhao Hu. "Regioselectivity in Lewis acids catalyzed X–H (O, S, N) insertions of methyl styryldiazoacetate with benzyl alcohol, benzyl thiol, and aniline." Tetrahedron Letters 48, no. 23 (2007): 3975–77. http://dx.doi.org/10.1016/j.tetlet.2007.04.046.

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31

Boukallaba, K., A. Elachqar, A. El Hallaoui та ін. "Synthesis of α-Heterocyclic α-Aminophosphonates, Part II: Morpholine, Piperidine, Pyrrolidine, Tetrahydrofurylmethylamine, N-Benzyl-N-Methylamine, and Aniline Derivatives". Phosphorus, Sulfur, and Silicon and the Related Elements 182, № 5 (2007): 1045–52. http://dx.doi.org/10.1080/10426500601093739.

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32

Bacsa, Ildikó, Dávid Szemerédi, János Wölfling, Gyula Schneider, Lilla Fekete, and Erzsébet Mernyák. "The first Pd-catalyzed Buchwald–Hartwig aminations at C-2 or C-4 in the estrone series." Beilstein Journal of Organic Chemistry 14 (May 4, 2018): 998–1003. http://dx.doi.org/10.3762/bjoc.14.85.

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A facile Pd-catalyzed C(sp2)–N coupling to provide a range of 2- or 4-[(subst.)phenyl]amino-13α-estrone derivatives has been achieved under microwave irradiation. The reactions were mediated with the use of Pd(OAc)2 as a catalyst and KOt-Bu as a base in the presence of X-Phos as a ligand. The desired products have been obtained in good to excellent yields. The nature and the position of the aniline substituent at the aromatic ring influenced the outcome of the couplings. 2-Amino-13α-estrone was also synthesized in a two-step protocol including an amination of 2-bromo-13α-estrone 3-benzyl ether

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33

Nasution, Risna Lenita, and Diky Setya Diningrat. "Inventarisasi Senyawa Antiinflamasi Pada Tumbuhan Buasbuas (Premna Pubescens Blume) Dengan Metode Gas Chromatography-Mass Spektrometri." Kalwedo Sains (KASA) 1, no. 1 (2020): 50–56. http://dx.doi.org/10.30598/kasav1i1p50-56.

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Tujuan dari penelitian ini untuk mengidentifikasi dan membandingkan jenis senyawa antiinflamasi pada daun muda, daun tua, buah dan tangkai daun tanaman buasbuas (Premna pubescens Blume) dengan metode Gas Cromatografy Mass Spectrometry (GC-MS). Masing-masing sampel diekstrak menggunakan metode maserasi dengan perendaman etanol 96% di dryer untuk mendapatkan ekstrak etanol berbentuk pasta. Pasta di analisis menggunakan (GC-MS). Data hasil GC-MS dianalisis menggunkan software Pubchem. Hasil penelitian menunjukkan senyawa antiinflamasi terbanyak pada daun tua dengan 11 jenis senyawa bioaktif diant

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34

Wu, Shouting, Xi Liang, Fang Luo, et al. "Synthesis, Crystal Structure and Bioactivity of Phenazine-1-carboxylic Acylhydrazone Derivatives." Molecules 26, no. 17 (2021): 5320. http://dx.doi.org/10.3390/molecules26175320.

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A phenazine-1-carboxylic acid intermediate was synthesized from the reaction of aniline and 2-bromo-3-nitro-benzoic acid. It was then esterified and reacted with hydrazine hydrate to afford phenazine-1-carboxylic hydrazine. Finally, 10 new hydrazone compounds 3a–3j were obtained by the condensation reaction of phenazine-1-carboxylic acid hydrazide and the respective aldehyde-containing compound. The structures were characterized by 1H and 13C NMR spectroscopy, MS and single crystal X-ray diffraction. The antitumor activity of the target compounds in vitro (HeLa and A549) was determined by thia

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35

Huang, Xiubing, Liping Liu, Hongyi Gao, Wenjun Dong, Mu Yang, and Ge Wang. "Hierarchically nanostructured MnCo2O4 as active catalysts for the synthesis of N-benzylideneaniline from benzyl alcohol and aniline." Green Chemistry 19, no. 3 (2017): 769–77. http://dx.doi.org/10.1039/c6gc02065h.

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Appropriate and similar ratios of Mn<sup>2+</sup>/Mn<sup>3+</sup> and Co<sup>2+</sup>/Co<sup>3+</sup> with excellent synergistic effects contribute to the high catalytic activity of MnCo<sub>2</sub>O<sub>4</sub>.

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36

Ding, C., H. Wang, B. Lu, J. Zhao, and Q. Cai. "Studies on Deactivation of Iron Oxide Catalyst in Solvent-Free N-Benzylation of Aniline with Benzyl Chloride." Kinetics and Catalysis 61, no. 5 (2020): 768–74. http://dx.doi.org/10.1134/s0023158420050031.

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37

Shi, Xinghao, Lei Chen, Biao Meng, et al. "Unveiling the enzyme-like acidic microenvironment in FER zeolite for N-alkylation of aniline with benzyl alcohol." Colloids and Surfaces A: Physicochemical and Engineering Aspects 726 (December 2025): 137847. https://doi.org/10.1016/j.colsurfa.2025.137847.

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38

Mahmudov, Ibadulla, Yeliz Demir, Yusuf Sert, et al. "Synthesis and inhibition profiles of N-benzyl- and N-allyl aniline derivatives against carbonic anhydrase and acetylcholinesterase – A molecular docking study." Arabian Journal of Chemistry 15, no. 3 (2022): 103645. http://dx.doi.org/10.1016/j.arabjc.2021.103645.

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39

Pradip, P. Deohate, and N. Berad B. "The convenient microwave-assisted synthesis, characterization and structural study of substituted bis-[1,2,4]-dithiazolidines." Journal of Indian Chemical Society Vol. 91, Jul 2014 (2014): 1361–64. https://doi.org/10.5281/zenodo.5726594.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India Department of Chemistry, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-440 033, Maharashtra, India <em>E-mail </em>: pradip222091@yahoo.co.in <em>Manuscript received online 05 December 2012, revised 21 February 2014, accepted 28 February 2014</em> A convenient synthesis of substituted bis-[1,2,4]-dithiazolidines has been developed by using the environmentfriendly technique of microwave irradiation. The microwave-assisted synthesis of several members of the titled class

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Şahin, Neslihan, Christophe Gourlaouen, and David Sémeril. "Effect of the Positioning of Metal Centers on a Cavitand in the Ruthenium-Catalyzed N-Alkylation of Amines." Molecules 30, no. 4 (2025): 951. https://doi.org/10.3390/molecules30040951.

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Two bis-ruthenium(II) complexes, namely N,N′-{5,17-diamino-4(24),6(10),12(16),18(22)-tetramethylenedioxy-2,8,14,20-tetrapentylresorcin[4]arene}-bis-[dichloro-(p-cymene)-ruthenium(II)] (1) and N,N′-{5,11-diamino-4(24),6(10),12(16), 18(22)-tetramethylenedioxy-2,8,14,20-tetrapentylresorcin[4]arene}-bis-[dichloro-(p-cymene)-ruthenium(II)] (2) were synthesized and tested as catalysts in the N-alkylation of primary amines with arylmethyl alcohol using the green “hydrogen borrowing” methodology. The catalytic results were compared with those obtained when the N-{5-amino-4(24),6(10),12(16),18(22)-tetr

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R., C. MAURYA, D. MISHRA D., JAISWAL S., and B. KHAN J. "Synthesis and Characterisation some Mixed-Ligand Cyanonitrosyl {CrNO}5 Complexes of Chromium(I) with some Aniline and 2-Pyrazolin-5-one Derivatives." Journal of Indian Chemical Society Vol. 69, Dec 1992 (1992): 801–3. https://doi.org/10.5281/zenodo.6017694.

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Coordination Chemistry Laboratory, Department of P. G. Studies and Research in Chemistry, R. D. University, Jabalpur-482 001 <em>Manuscript received 4 May 1990, revised 12 August 1992, accepted 18 August 1992</em> Mixed-ligand hexacoordinated cyanonitrosyl {CrNO}<sup>5</sup> complexes of chromium(I) of the compositions, Cr(NO) (CN)<sub>2</sub>(L)2 (H<sub>2</sub>O)] (where L=<em>N</em>-methylaniline, <em>N</em>-ethyl-<em>o</em>-toluidine, <em>N</em>-ethyl-<em>p</em>-tolnidine,<em> N,N</em>-dimethyl-<em>m</em>-toluidine or <em>N</em>-benzyl-<em>N</em>-ethylaniline) and [Cr(NO) (CN)<sub>2</s

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Huang, Qiang, and Baozhong Zheng. "Facile Synthesis of Benzaldehyde-Functionalized Ionic Liquids and Their Flexible Functional Group Transformations." Organic Chemistry International 2012 (November 12, 2012): 1–5. http://dx.doi.org/10.1155/2012/208128.

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Three benzaldehyde-functionalized ionic liquids were readily synthesized by quaternization of N-alkylimidazole with benzaldehyde-functionalized alkyl bromides under microwave irradiation in good yield. These aldehyde-functionalized ionic liquids could easily be oxidized in the presence of H2O2/KOH or be reduced by NaBH4 leading to the formation of the corresponding carboxyl-functionalized ionic liquids or benzylic alcohol-functionalized ionic liquids. In addition, the condensations of these functionalized ones with hydrazine hydrate and with aniline under reductive amination conditions were de

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Tušek-Božić, Ljerka. "Infrared spectra of monoalkyl (α-anilino-N-benzyl)phosphonates, their sodium salts and dipalladium(II) metallocyclic complexes". Vibrational Spectroscopy 28, № 2 (2002): 235–41. http://dx.doi.org/10.1016/s0924-2031(01)00137-0.

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Ćurić, Manda, Ljerka Tušek-Božić та Pietro Traldi. "Spectroscopic and thermal study of dialkyl (α-anilino-N-benzyl)phosphonates and their palladium(II) dichloride adducts". Polyhedron 17, № 4 (1998): 531–38. http://dx.doi.org/10.1016/s0277-5387(97)00340-9.

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Schmid, Martin, Birgit Waldner, Michael Schnürch, Marko D. Mihovilovic, and Peter Stanetty. "Studying competitive lithiations at alpha-, ortho-, and benzylic positions in various N-protected aniline derivatives." Tetrahedron 67, no. 16 (2011): 2895–904. http://dx.doi.org/10.1016/j.tet.2011.02.056.

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Xia, Xinyu, Shankai Hou, Yong Guo, Xiaohui Liu, and Yanqin Wang. "Catalytic N-Alkylation of Benzyl Alcohol and Aniline on Nb₂O₅ Catalyst." Acta Chimica Sinica 83, no. 3 (2025): 212. https://doi.org/10.6023/a25010007.

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Liu, Leng, Jun Li, Xiuling Chen, et al. "Efficient Construction of N-heterocycles from Benzylic Ethers/Alcohols and o-Substituted Anilines without Using any Catalyst and Additive." HETEROCYCLES 94, no. 1 (2017): 86. http://dx.doi.org/10.3987/com-16-13587.

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Sreenivasulu, Peta, Nagabhatla Viswanadham, and Sandeep K. Saxena. "Facile synthesis of mesoporous aluminosilicate nanoparticles for the selective production of N-benzylidenaniline in a solvent-free reaction of aniline with benzyl alcohol." J. Mater. Chem. A 2, no. 20 (2014): 7354–59. http://dx.doi.org/10.1039/c3ta15323a.

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We report a simple method for the synthesis of mesoporous aluminosilicate nanoparticles by adopting a novel concept of using TPABr as a precursor for the structure directing agent through a solvent-free physical mixing method.

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Madia, Valentina Noemi, Alice Nicolai, Antonella Messore, et al. "Design, Synthesis and Biological Evaluation of New Pyrimidine Derivatives as Anticancer Agents." Molecules 26, no. 3 (2021): 771. http://dx.doi.org/10.3390/molecules26030771.

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Background: Anticancer drug resistance is a challenging phenomenon of growing concern which arises from alteration in drug targets. Despite the fast speed of new chemotherapeutic agent design, the increasing prevalence of this phenomenon requires further research and treatment development. Recently, we reported a new aminopyrimidine compound—namely RDS 344—as a potential innovative anticancer agent. Methods: Herein, we report the design, synthesis, and anti-proliferative activity of new aminopyrimidine derivatives structurally related to RDS 3442 obtained by carrying out substitutions at posit

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Mikhniuk, O. N., S. M. Leschev, and P. A. Kasyanchik. "Distribution constants and group increments of organic substances in the extraction systems of water saline–hexane." Proceedings of the National Academy of Sciences of Belarus, Chemical Series 56, no. 2 (2020): 158–65. http://dx.doi.org/10.29235/1561-8331-2020-56-2-158-165.

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In the extraction systems of hexane–aqueous solutions of potassium carbonate, ammonium sulfate and sodium chloride, the distribution of a number of organic compounds (benzyl alcohol, tetrahydrofuran, phenol, aniline, pyridine, pyridazine, pyrimidine, n-butylamine, diethylamine, triethylamine, benzylamine) was studied. It was shown that sodium chloride, the most frequently used as a salting out agent, is noticeably inferior in salting ability to potassium carbonate, dipotassium phosphate and ammonium sulfate, since it contains singly charged ions with a relatively low charge density. Using the

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