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Journal articles on the topic 'Diphenylamine derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Ito, Akihiro, Ken-ichi Ota, Kazunari Yoshizawa, Kazuyoshi Tanaka, and Tokio Yamabe. "Ab initio MO study of diphenylamine derivatives: diphenylamine, diphenylaminium, diphenylaminyl and diphenylnitroxide." Chemical Physics Letters 223, no. 1-2 (1994): 27–34. http://dx.doi.org/10.1016/0009-2614(94)00416-1.

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2

Begunov, Roman S., and Alexander I. Khlopotinin. "BENZOTRIAZOLE DERIVATIVES OF DIPHENYLAMINE ARE NEW UV RADIATION ABSORBERS." ChemChemTech 68, no. 5 (2025): 112–20. https://doi.org/10.6060/ivkkt.20256805.7200.

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In order to develop UV absorbers with improved extinction coefficients, previously obtained UV absorbers 1-(2-aminophenyl)-1H- and 2-(2-aminophenyl)-2H-benzotriazoles functionalization was carried out through aromatic nucleophilic substitution reaction with nitrohalogenarenes and followed reduction of the obtained nitrodiphenylamines. The conditions for these reactions were selected to synthesize target products with high yield. As a result, 10 new diphenylamine derivatives containing 1H- or 2H-benzotriazole cycles were synthesized. The structures of the obtained multifunctional compounds were

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3

Rudell, David, James Mattheis, and John Fellman. "Diphenylamine and Diphenylamine Derivative Content of `Granny Smith' Peel: Influence of Ethylene Action and Regular or Controlled Atmosphere Storage Duration." HortScience 40, no. 4 (2005): 1144B—1144. http://dx.doi.org/10.21273/hortsci.40.4.1144b.

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Diphenylamine (DPA) is used for superficial scald control in apple fruit. A number of DPA derivatives resulting from C-nitration, C-hydroxylation, O-methylation, and N-nitrosation can be present in DPA-treated apple fruit after storage. The presence of the compounds may be indicative of metabolic processes that lead to scald development. Therefore, apple peel DPA and DPA derivative content in fruit treated at harvest with DPA or DPA plus 1-methylcyclopropene (1-MCP) was assayed upon removal of fruit from controlled atmosphere (CA) and regular atmosphere (RA) storage and during a 14-d post-stor

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4

Huang, Tai-Hsiang, and Jiann T. Lin. "Tunable Dipolar Acenaphthopyrazine Derivatives Containing Diphenylamine." Chemistry of Materials 16, no. 25 (2004): 5387–93. http://dx.doi.org/10.1021/cm049069m.

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5

Janovec, Ladislav, Jana Janočková, Mária Matejová, et al. "Proliferation inhibition of novel diphenylamine derivatives." Bioorganic Chemistry 83 (March 2019): 487–99. http://dx.doi.org/10.1016/j.bioorg.2018.10.063.

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6

Kumar, Arvind, and Arun K. Mishra. "Synthesis, Toxicity Profile and Pharmacological Evaluation of Some New N,N-Diphenyl Amine Derivatives with Special Reference to Analgesic and Anti-inflammatory Activity." Letters in Organic Chemistry 17, no. 7 (2020): 560–70. http://dx.doi.org/10.2174/1570178617666191220150024.

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The present work was aimed to synthesize eight new diphenylamine derivatives by the reactions of 2-chloro-N-(4-(diphenyl amino) thiazol-2-yl)acetamide with substituted phenols in the chloroform along with anhydrous potassium carbonate and potassium iodide. The structures of newly synthesized compounds were characterized by IR, NMR, Mass and elemental analysis techniques. Toxicity profile (acute and subacute oral toxicity) and biological activity (analgesic and anti-inflammatory activity) of the synthesized derivatives was performed. Findings of the present work suggested that the synthesized c

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7

Tretiakov, I. V., and J. R. Cable. "Electronic spectroscopy and molecular structure of jet-cooled diphenylamine and diphenylamine derivatives." Journal of Chemical Physics 107, no. 23 (1997): 9715–25. http://dx.doi.org/10.1063/1.475268.

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8

Julianto, T. S., F. J. Rachmawaty, H. A. Tamhid, and B. S. Putri. "THE POTENTIAL ANTIMALARIAL DRUG OF ARYL AMINO ALCOHOL DERIVATIVES FROM EUGENOL: SYNTHESIS, in-vitro AND in-silico ANALYSIS OF BIOACTIVITY." RASAYAN Journal of Chemistry 16, no. 03 (2023): 1425–34. http://dx.doi.org/10.31788/rjc.2023.1636940.

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Malaria is a significant cause of death in numerous countries, and the discovery of effective drugs is crucial. In this research, a new method was employed to synthesize a derivative of aryl amino alcohol using eugenol. Initially, an epoxide compound called 2-methoxy-4-(oxiran-2-ylmethyl) phenol was synthesized from eugenol by reacting it with peroxyacetic acid in dichloromethane. Subsequently, the epoxide compound was subjected to a reaction with various amine compounds, including aniline, naphthylamine, and diphenylamine for 10 minutes under 100 W microwave conditions, resulting in the produ

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9

Salahifar, Eslam, and Davood Nematollahi. "Electrochemical generation of a Michael acceptor: a green method for the synthesis of 4-amino-3-(phenylsulfonyl)diphenylamine derivatives." New Journal of Chemistry 39, no. 5 (2015): 3852–58. http://dx.doi.org/10.1039/c5nj00087d.

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10

Chen, Sin-Yu, Ya-Wen Chiu та Guey-Sheng Liou. "Substituent effects of AIE-active α-cyanostilbene-containing triphenylamine derivatives on electrofluorochromic behavior". Nanoscale 11, № 17 (2019): 8597–603. http://dx.doi.org/10.1039/c9nr02692d.

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Four aggregation-induced emission- and electro-active cyanostilbene-based diphenylamine-containing derivatives were synthesized to investigate the photoluminescence properties, and electrochromic and electrofluorochromic behavior of gel-type devices.

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11

Mayer, Szabolcs, Péter Keglevich, Péter Ábrányi-Balogh, et al. "Synthesis and In Vitro Anticancer Evaluation of Novel Chrysin and 7-Aminochrysin Derivatives." Molecules 25, no. 4 (2020): 888. http://dx.doi.org/10.3390/molecules25040888.

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Chrysin is a naturally occurring flavonoid with mild anticancer activity. In this paper we report the synthesis of new chrysin derivatives alkylated with N-phenylchloroacetamides in position 7. A novel method was developed for the preparation of 7-aminochrysin derivatives via the Smiles rearrangement, resulting in diphenylamine-type compounds. In silico studies of the Smiles rearrangement were performed. We also present the in vitro antiproliferative activity of the synthesized compounds against 60 human tumor cell lines (NCI60). The most potent derivative exhibited nanomolar antitumor activit

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12

Chávez-Riveros, Alejandra, Eduardo Hernández-Vázquez, Antonio Nieto-Camacho, Teresa Ramírez-Apan, and Luis D. Miranda. "Synthesis of diphenylamine macrocycles and their anti-inflammatory effects." Organic & Biomolecular Chemistry 17, no. 6 (2019): 1423–35. http://dx.doi.org/10.1039/c8ob03121e.

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A collection of fourteen diphenylamine macrocyclic derivatives containing a peptide chain with different substituents was synthesized using a protocol of two Ugi four component reactions (Ugi-4CR) and a Buchwald–Hartwig macrocyclization.

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13

Zhang, Yun, Chun Kou, Junjie Zhang, et al. "Crosslinked and dopant free hole transport materials for efficient and stable planar perovskite solar cells." Journal of Materials Chemistry A 7, no. 10 (2019): 5522–29. http://dx.doi.org/10.1039/c8ta12060a.

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A series of crosslinked diphenylamine derivatives have been developed and employed as hole transport materials in inverted p–i–n planar perovskite solar cells, which exhibit the significantly improved device efficiency and stability.

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14

Abraham, Silja, Gayathri Prabhu T. Ganesh, Sunil Varughese, Biswapriya Deb, and Joshy Joseph. "Cross-Linkable Fluorene-Diphenylamine Derivatives for Electrochromic Applications." ACS Applied Materials & Interfaces 7, no. 45 (2015): 25424–33. http://dx.doi.org/10.1021/acsami.5b08218.

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15

Drzyzga, Oliver. "Diphenylamine and derivatives in the environment: a review." Chemosphere 53, no. 8 (2003): 809–18. http://dx.doi.org/10.1016/s0045-6535(03)00613-1.

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16

Drzyzga, O., A. Schmidt, and K. Blotevogel. "Reduction of Nitrated Diphenylamine Derivatives under Anaerobic Conditions." Applied and environmental microbiology 61, no. 9 (1995): 3282–87. http://dx.doi.org/10.1128/aem.61.9.3282-3287.1995.

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17

Kim, Byong-Sam, Dong-Geun Jung, Kiseok Kim, Tae-Jin Lee, Jae-Chang Kim, and Dong-Hyun Kim. "Synthesis of diphenylamine derivatives on Pd/C catalyst." Korean Journal of Chemical Engineering 15, no. 5 (1998): 522–26. http://dx.doi.org/10.1007/bf02707103.

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18

Kumar, Rohit, Sushil Kumar, and Mohammad Asif Khan. "Synthesis and Pharmacological Evaluation of 2-(4-(3 (Substituted Phenyl) Acryloyl) Phenoxy)-N, N Diphenylacetamides." Journal of Drug Delivery and Therapeutics 10, no. 5 (2020): 274–92. http://dx.doi.org/10.22270/jddt.v10i5.4326.

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Recently a series of Schiff bases of diphenylamine derivatives have been synthesized and evaluated in vitro for their antibacterial activity against pathogenic both Gram-positive bacteria B. subtitles and Gram-negative bacteria E. coli using ciprofloxacin as standard drug at conc. of 50 μg/ml and 100 μg/ml. Literature review revels that chalcones possesses various biological activities like antimicrobial, antiviral, anti-inflammatory, anticancer and sedative etc. Therefore the present study was designed on synthesis and pharmacological evaluation of 2-(4-(3 (Substituted Phenyl) Acryloyl) Pheno

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19

Aleksandrova, Yulia R., Natalia S. Nikolaeva, Inna A. Shagina, et al. "N-Aryl Benzimidazole and Benzotriazole Derivatives and Their Hybrids as Cytotoxic Agents: Design, Synthesis and Structure–Activity Relationship Studies." Molecules 29, no. 22 (2024): 5360. http://dx.doi.org/10.3390/molecules29225360.

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The era of chemotherapy began in the 1940s, which is the basis of traditional antitumor approaches and, being one of the most high-tech treatment methods, is still widely used to treat various types of cancer. A promising direction in modern medicinal chemistry is currently the creation of hybrid molecules containing several pharmacophore fragments of different structures. This strategy is successfully used to increase the therapeutic efficacy of cytotoxic agents and reduce side effects. In this work, we synthesized 10 1-aryl derivatives of benzimidazole and benzotriazole and 11 hybrids based

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20

Sharma, Nidhi, Michael Yin Wong, David Hall, et al. "Exciton efficiency beyond the spin statistical limit in organic light emitting diodes based on anthracene derivatives." Journal of Materials Chemistry C 8, no. 11 (2020): 3773–83. http://dx.doi.org/10.1039/c9tc06356k.

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21

Kapoor, D., and P. Gupta. "Synthesis and Characterization of Phenothiazine Derivatives." Pharmaceutical and Chemical Journal 3, no. 2 (2016): 57–70. https://doi.org/10.5281/zenodo.13742728.

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A series of new phenothiazine derivatives have been synthesized in which diphenylamine on treatment with sulphur give 10<em>H</em>-phenothiazinewhich on reaction with ethylchloro acetate yielded 2-(10<em>H</em>-phenothiazin-10-yl)acetate which on further treatment with hydrazine hydrate produced 2-(10<em>H</em>-phenothiazin-10-yl) acetohydrazide<strong>. </strong>Condensation of chief intermediate with various benzaldehyde derivatives afforded<em> N'</em>-(substitutedbenzylidene)-2-(10<em>H-</em>phenothiazin-10-yl) acetohydrazide. All the synthesized derivatives have been characterized by FTIR

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22

Kumar, Arvind, and ArunK Mishra. "Synthesis and antimicrobial activity of some new diphenylamine derivatives." Journal of Pharmacy and Bioallied Sciences 7, no. 1 (2015): 81. http://dx.doi.org/10.4103/0975-7406.148774.

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23

Mandare, Narendra, Ponnusamy Shanmugam, Mahesh Sundararajan, and Sharmistha Dutta Choudhury. "Unravelling the photophysics of triphenylamine and diphenylamine dyes: a comprehensive investigation with ortho-, meta- and para-amido substituted derivatives." New Journal of Chemistry 44, no. 44 (2020): 19061–75. http://dx.doi.org/10.1039/d0nj04569a.

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24

Gaber, Abd El-Aal M., Morsy M. Aly, and Ahmed A. Atalla. "Thermolysis of some thiourea derivatives." Collection of Czechoslovak Chemical Communications 56, no. 10 (1991): 2183–87. http://dx.doi.org/10.1135/cccc19912183.

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Thermolysis of N/benzoyl-N’,N’-diphenylthiourea (BDTU)(I) at 250°C gives NH3, H2S, H2O, benzaldehyde, benzil, benzonitrile, diphenylamine, diphenylcyanamide, 2-phenylbenzimidazole, benzoyl isothiocyanate, carbazole and 2-phenylbenzthiazole, whereas, thermolysis of N-benzoyl-N'-o-tolylthiourea (BTTU) (II) under the same conditions afford NH3, H2S, H2O, benzaldehyde, benzil, benzonitrile, o-toluidine, o-tolyl isothiocyanate, o-tolylcyanamide, benzoyl isothiocyanate and N,N’-di-o-tolylthiourea. The main feature of these thermolyses is homolysis of the amide and thioamide bonds providing free radi

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25

Wang, Shengpei, Shasha Yu, Jianxiang Feng, and Shenggao Liu. "Multifunctional lubricant additive based on difluoroboron derivatives of a diphenylamine antioxidant." RSC Advances 9, no. 60 (2019): 35059–67. http://dx.doi.org/10.1039/c9ra05490a.

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26

Li, Huichao, Aiying Guan, Guang Huang, et al. "Design, synthesis and structure–activity relationship of novel diphenylamine derivatives." Bioorganic & Medicinal Chemistry 24, no. 3 (2016): 453–61. http://dx.doi.org/10.1016/j.bmc.2015.09.032.

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27

Xia, Wujiong, Xinxin Zhao, Ming Chen, Binbin Huang, Chao Yang, and Yuan Gao. "Photoinduced Cross-Coupling of Amines with 1,2-Diiodobenzene and Its Application in the Synthesis of Carbazoles." Synthesis 50, no. 15 (2018): 2981–89. http://dx.doi.org/10.1055/s-0037-1609444.

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A facile and efficient process for the preparation of various tertiary aminobenzenes and carbazole derivatives via photoinduced cross-coupling of amines with 1,2-diiodobenzene is reported. Mechanistic investigations indicate that the transformation proceeds via nucleophilic addition of an amine to the benzyne intermediate accompanied with a proton transfer process, followed by an oxidative cyclization of the generated diphenylamine to furnish the corresponding carbazole products.

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28

Seo, Jiyoung, Won-Kyung Moon, and Man-Jae Bae. "A Study on the Analysis of Derivatives of Ammunition Stockpile Stabilizer(DPA) using High Performance Liquid Chromatography." Journal of the Korea Academia-Industrial cooperation Society 25, no. 9 (2024): 392–400. http://dx.doi.org/10.5762/kais.2024.25.9.392.

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29

CHOI, H. J., M. S. CHO, J. W. KIM, R. M. WEBBER, and M. S. JHON. "EFFECT OF IONIC AND NONIONIC SUBSTITUENTS ON THE ELECTRORHEOLOGICAL CHARACTERISTICS OF POLYANILINE DERIVATIVES." International Journal of Modern Physics B 15, no. 06n07 (2001): 988–95. http://dx.doi.org/10.1142/s0217979201005519.

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We report our experimental results on the electrorheological (ER) characteristics of ER fluids consisting of suspensions of semiconducting polyaniline and copolyaniline particles in silicone oil. Ionic sodium diphenylamine sulfonate and nonionic o-ethoxyaniline were introduced to synthesize copolyanilines, i.e. N-substituted copolyaniline and poly (aniline-co-o-ethoxyaniline), respectively. ER fluids using these particles were compared. ER fluids, which contain the ionic copolymer, showed the highest ER performance among polyaniline and its copolymer systems. This result was interpreted in ter

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30

Chen, Wen Chang, and Samson A. Jenekhe. "New polyaniline derivatives: poly(4,4'-diphenylamine methylenes) and poly(4,4'-diphenylimine methines)." Macromolecules 25, no. 22 (1992): 5919–26. http://dx.doi.org/10.1021/ma00048a010.

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31

Abraham, Silja, Sreejith Mangalath, Deepika Sasikumar, and Joshy Joseph. "Transmissive-to-Black Electrochromic Devices Based on Cross-Linkable Tetraphenylethene-Diphenylamine Derivatives." Chemistry of Materials 29, no. 23 (2017): 9877–81. http://dx.doi.org/10.1021/acs.chemmater.7b03319.

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32

Li, Fusheng, Baodong Zhao, Yu Chen, Yufei Zhang, Tao Wang, and Song Xue. "Synthesis, characterization, and nonlinear optical (NLO) properties of truxene-cored diphenylamine derivatives." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 185 (October 2017): 20–26. http://dx.doi.org/10.1016/j.saa.2017.05.030.

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33

Curtis, Neville J. "Isomer distribution of nitro derivatives of diphenylamine in gun propellants: Nitrosamine Chemistry." Propellants, Explosives, Pyrotechnics 15, no. 5 (1990): 222–30. http://dx.doi.org/10.1002/prep.19900150509.

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34

Ikpa, Chinyere B. C., Samuel O. Onoja, and Anastasia O. Okwaraji. "Synthesis And Antibacterial Activities Of Benzothiazole Derivatives Of Sulphonamides." Acta Chemica Malaysia 4, no. 2 (2020): 55–57. http://dx.doi.org/10.2478/acmy-2020-0009.

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AbstractThis study aims to synthesize hybrid compounds “via” the coupling of sulphonamide and benzothiazole into one structure that may have improved antibacterial property. The N-(biphenyl-4-yl) thiourea (1) used for the synthesis of the targeted sulphonamides was obtained by reacting diphenylamine and ammonium thiocyanate at room temperature. Cyclization of N-(biphenyl-4-yl)thiourea gave 2-amino-6-phenylbenzothiazole (2) which reacted with benzenesulphonyl chloride and para-toulene sulphonyl chloride to give the targeted sulphonamides (3a & 3b). The synthesized compounds were characteris

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35

Sathe, B. S., E. Jaychandran, G. M. Sreenivasa, and V. A. Jagtap. "Antimycobacterial Activity of Some Synthesized Fluorinated Benzothiazolo Imidazole Compounds." E-Journal of Chemistry 8, no. 2 (2011): 830–34. http://dx.doi.org/10.1155/2011/581429.

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4-Fluoro-3-chloroanilline treated with potassium thiocyanate in presence of glacial acetic acid and bromine was converted into 2-amino-6-fluoro-7-chlorobenzothiazole, resulting into 2-amino benzothiazole. The synthesized compound in presence of 2-phenyl-4-benzylidine-5-oxazolinone refluxed in pyridine to obtain 2-(2-phenyl-4-benzylidenyl-5-oxo-imidazolin-1-yl amino)-6-fluoro-7-substituted(1,3)benzothiazoles. The above said compound was treated withortho, metaandpara nitroanillines, ortho, meta, parachloroanillines, morpholino, piperazine, diphenylamine in the presence of DMF to obtain differen

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36

Rudell, David R., James P. Mattheis та John K. Fellman. "Relationship of Superficial Scald Development and α-Farnesene Oxidation to Reactions of Diphenylamine and Diphenylamine Derivatives in Cv. Granny Smith Apple Peel". Journal of Agricultural and Food Chemistry 53, № 21 (2005): 8382–89. http://dx.doi.org/10.1021/jf0512407.

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37

Sutherland, Daniel R., Nidhi Sharma, Georgina M. Rosair, Ifor D. W. Samuel, Ai-Lan Lee, and Eli Zysman-Colman. "Synthesis and optoelectronic properties of benzoquinone-based donor–acceptor compounds." Beilstein Journal of Organic Chemistry 15 (December 4, 2019): 2914–21. http://dx.doi.org/10.3762/bjoc.15.285.

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Herein, we report a mild and efficient palladium-catalyzed C–H functionalization method to synthesize a series of benzoquinone (BQ)-based charge-transfer (CT) derivatives in good yields. The optoelectronic properties of these compounds were explored both theoretically and experimentally and correlations to their structures were identified as a function of the nature and position of the donor group (meta and para) attached to the benzoquinone acceptor. Compound 3, where benzoquinone is para-conjugated to the diphenylamine donor group, exhibited thermally activated delayed fluorescence (TADF) wi

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38

Zubrickė, Irma, Ilona Jonuškienė, Kristina Kantminienė, Ingrida Tumosienė, and Vilma Petrikaitė. "Synthesis and In Vitro Evaluation as Potential Anticancer and Antioxidant Agents of Diphenylamine-Pyrrolidin-2-one-Hydrazone Derivatives." International Journal of Molecular Sciences 24, no. 23 (2023): 16804. http://dx.doi.org/10.3390/ijms242316804.

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The title compounds were synthesized by the reaction of 5-oxo-1-(4-(phenylamino)phenyl)pyrrolidine-3-carbohydrazide with various aldehydes bearing aromatic and heterocyclic moieties and acetophenones, and their cytotoxicity was tested via MTT assay against human triple-negative breast cancer MDA-MB-231, human melanoma IGR39, human pancreatic carcinoma Panc-1, and prostate cancer cell line PPC-1. Furthermore, the selectivity of compounds towards cancer cells compared to fibroblasts was also investigated. Four compounds were identified as the most promising anticancer agents out of a series of p

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39

Ohuchi, Kazuo, Masako Watanabe, Yukari Fukui, Noriyasu Hirasawa, Tsuneo Ozeki, and Susumu Tsurufuji. "The effect of diphenylamine derivatives on arachidonic acid metabolism in rat peritoneal macrophages." Prostaglandins, Leukotrienes and Medicine 28, no. 1 (1987): 15–23. http://dx.doi.org/10.1016/0262-1746(87)90043-6.

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40

Espinoza, Edgard O'N, and John I. Thornton. "Characterization of smokeless gunpowder by means of diphenylamine stabilizer and its nitrated derivatives." Analytica Chimica Acta 288, no. 1-2 (1994): 57–69. http://dx.doi.org/10.1016/0003-2670(94)85116-6.

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41

Yu, Jiang, Peiting Zhou, Wu Du, et al. "Metabolically stable diphenylamine derivatives suppress androgen receptor and BET protein in prostate cancer." Biochemical Pharmacology 177 (July 2020): 113946. http://dx.doi.org/10.1016/j.bcp.2020.113946.

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42

Chen, Fangyi, Wanxi Zhang, Zijian Liu, et al. "Enhancement of intramolecular charge transfer strength in diphenylamine substituted symmetric 1,3,4-oxadiazole derivatives." RSC Advances 9, no. 1 (2019): 1–10. http://dx.doi.org/10.1039/c8ra08439d.

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43

Shimizu, Toshiyuki, Yasunari Fujiwara, Tatsushi Osawa, et al. "Orally active anti-proliferation agents: novel diphenylamine derivatives as FGF-R2 autophosphorylation inhibitors." Bioorganic & Medicinal Chemistry Letters 14, no. 4 (2004): 875–79. http://dx.doi.org/10.1016/j.bmcl.2003.12.019.

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44

Aksungur, Tuğçe, Fatma Erol, Nurgül Seferoğlu, and Zeynel Seferoğlu. "Experimental and theoretical studies on monoazo dye including diphenylamine and N-methyldiphenylamine derivatives." Journal of Molecular Structure 1217 (October 2020): 128449. http://dx.doi.org/10.1016/j.molstruc.2020.128449.

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45

Xu, Zhihui, Yanlin Yang, Jiao Liu, Yaoxin Zhang, Hongquan Zhang, and Ming-Xing Zhang. "Asymmetric phenothiazine derivatives modified with diphenylamine and carbazole: Photophysical properties and hypochlorite sensing." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 340 (November 2025): 126346. https://doi.org/10.1016/j.saa.2025.126346.

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46

Zhao, Xuelian, You Li, Fangyi Chen, et al. "Intramolecular charge transfer dynamics in the excited states of diphenylamine substituted 1,3,4-oxadiazole derivatives." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 267 (February 2022): 120463. http://dx.doi.org/10.1016/j.saa.2021.120463.

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47

Guan, Daokun, Shaofeng Sun, Jing Chen, et al. "Synthesis and Evaluation of Antitumor Activity of Sorafenib Derivatives Possessing Diphenylamine and Thiourea Structures." Chinese Journal of Organic Chemistry 38, no. 6 (2018): 1414. http://dx.doi.org/10.6023/cjoc201802005.

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48

Dale, Johannes, Line Vikersveen, Jorma Mattinen, et al. "The Reaction of Nitrobenzenes with Sodium Borohydride; a Novel Reductive Coupling to Diphenylamine Derivatives." Acta Chemica Scandinavica 42b (1988): 354–61. http://dx.doi.org/10.3891/acta.chem.scand.42b-0354.

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49

Sakalyte, Asta, Jurate Simokaitiene, Ausra Tomkeviciene, et al. "Effect of Methoxy Substituents on the Properties of the Derivatives of Carbazole and Diphenylamine." Journal of Physical Chemistry C 115, no. 11 (2011): 4856–62. http://dx.doi.org/10.1021/jp109643r.

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50

Capodilupo, Agostina-Lina, Viviana Vergaro, Gianluca Accorsi, et al. "A series of diphenylamine-fluorenone derivatives as potential fluorescent probes for neuroblastoma cell staining." Tetrahedron 72, no. 22 (2016): 2920–28. http://dx.doi.org/10.1016/j.tet.2016.04.012.

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