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Journal articles on the topic '2-Naphthylamine'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Jirman, Josef. "1H and 13C NMR Spectra of Technically Important Sodium 1- and 2-Aminonaphthalenesulfonates." Collection of Czechoslovak Chemical Communications 58, no. 6 (1993): 1378–87. http://dx.doi.org/10.1135/cccc19931378.

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The 1H and 13C NMR spectra of twenty-one technically important sulfonated 1- and 2-naphthylamines have been measured in deuterium oxide. The substituent chemical shifts (SCS) of a sulfonic acid group on naphthylamine skeleton have been calculated from the chemical shifts assigned.

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2

Weiss, Tobias, Thomas Brüning, and Hermann M. Bolt. "Dephenylation of the Rubber ChemicalN-Phenyl-2-Naphthylamine to Carcinogenic 2-Naphthylamine: A Classical Problem Revisited." Critical Reviews in Toxicology 37, no. 7 (2007): 553–66. http://dx.doi.org/10.1080/10408440701419637.

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3

Weiss, Tobias, Hermann M. Bolt, Gerhard Schlüter, et al. "Metabolic dephenylation of the rubber antioxidant N-phenyl-2-naphthylamine to carcinogenic 2-naphthylamine in rats." Archives of Toxicology 87, no. 7 (2013): 1265–72. http://dx.doi.org/10.1007/s00204-013-1025-5.

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4

Ciric-Marjanovic, Gordana, Nikola Cvjeticanin, Slavko Mentus, JaroslavaIvan Budinski-Simendic, and Ivan Krakovsky. "Electrochemical polymerization of 2-methyl-1-naphthylamine." Polymer Bulletin 50, no. 5-6 (2003): 319–26. http://dx.doi.org/10.1007/s00289-003-0174-8.

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5

Worobey, Brian L., and Brian J. shields. "Determination of Naptalam and Its Metabolite in Foods, as 1-Naphthylamine, Using Liquid Chromatography with Oxidative Electrochemical Detection." Journal of AOAC INTERNATIONAL 70, no. 6 (1987): 1021–24. http://dx.doi.org/10.1093/jaoac/70.6.1021.

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Abstract A new method is described for the determination of the herbicide naptalam and its metabolite l-naphthylamine in several foods. The method is sensitive, selective, and extremely rapid compared with previously reported methods. Liquid chromatography with electrochemical detection (LC/ECD) is used to determine l-naphthylamine produced from the metabolism or base hydrolysis of naptalam in asparagus, peaches, and cranberries. These foods were spiked with naptalam at 0.05 and 0.11 ppm and hydrolyzed with 30% NaOH with concomitant distillation of l-naphthylamine. Aliquots of the distillate w

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6

Winkelhaus, Daniel, Beate Neumann, and Norbert W. Mitzel. "An Intramolecular Boron Nitrogen Lewis Acid Base Pair on a Rigid Naphthyl Backbone." Zeitschrift für Naturforschung B 67, no. 6 (2012): 589–93. http://dx.doi.org/10.5560/znb.2012-0091.

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The reaction of (C6F5)2BCl with 8-lithio-N,N-dimethyl-1-naphthylamine (1) afforded the fivemembered ring system 8-bis(pentafluorophenyl)boryl-N,N-dimethyl-1-naphthylamine (2) with an intramolecular dative B-N bond. The compound was characterised by elemental analysis, NMR spectroscopy and single-crystal X-ray diffraction.

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7

Kozlov, N. G., A. P. Kadutskii, and A. V. Baranovskii. "Condensation of 2-naphthylamine or N-benzyl-2-naphthylamines with formaldehyde and methyl 2,2-dimethyl-4,6-dioxocyclohexane-3-carboxylate." Russian Journal of Organic Chemistry 48, no. 11 (2012): 1456–63. http://dx.doi.org/10.1134/s1070428012110085.

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8

Cheng, Long, Yan He, Yun Tian, et al. "Comparative biotoxicity of N-Phenyl-1-naphthylamine and N-Phenyl-2-naphthylamine on cyanobacteria Microcystis aeruginosa." Chemosphere 176 (June 2017): 183–91. http://dx.doi.org/10.1016/j.chemosphere.2017.02.110.

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9

Burlov, A. S., A. I. Uraev, P. V. Matuev, et al. "Metal chelates of benzeneazo-N-tosyl-2-naphthylamine." Russian Journal of Coordination Chemistry 34, no. 12 (2008): 904–10. http://dx.doi.org/10.1134/s1070328408120063.

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10

Xiao, Fuhong, Shanshan Yuan, Dahan Wang, Saiwen Liu, Huawen Huang, and Guo‐Jun Deng. "Thioesters as Bifunctional Reagents for 2‐Naphthylamine Sulfuracylation." Advanced Synthesis & Catalysis 361, no. 14 (2019): 3331–36. http://dx.doi.org/10.1002/adsc.201900301.

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11

Zhanaeva, T. A., O. E. Krivoshchekova, A. A. Semenov, and V. G. Minaeva. "N-phenyl-2-naphthylamine from Bupleurum aureum flowers." Chemistry of Natural Compounds 25, no. 3 (1989): 377. http://dx.doi.org/10.1007/bf00597731.

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12

Scharpé, S., I. De Meester, G. Vanhoof, et al. "Assay of dipeptidyl peptidase IV in serum by fluorometry of 4-methoxy-2-naphthylamine." Clinical Chemistry 34, no. 11 (1988): 2299–301. http://dx.doi.org/10.1093/clinchem/34.11.2299.

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Abstract A new fluorometric assay for determining dipeptidyl peptidase IV (DPP IV; EC 3.4.14.5) was developed. The synthetic substrate glycyl-L-proline-4-methoxy-2-naphthylamide (20 mmol/L), Tris buffer (50 mmol/L, pH 8.3), and serum (20 microL) are mixed and incubated. The reaction is stopped with citrate (100 mmol/L, pH 4.0) and the released 4-methoxy-2-naphthylamine is measured fluorometrically. The mean value of DPP IV activity in serum for 64 healthy subjects was 58 (SD 16) mumol of 4-methoxy-2-naphthylamine released per liter of serum per minute. The proposed procedure is sensitive, rapi

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13

Rosowsky, Andre, Ronald A. Forsch, Sherry F. Queener, and Joseph R. Bertino. "Synthesis of 2,4-Diaminopteridines with Bulky Lipophilic Groups at the 6-Position as Inhibitors of Pneumocystis carinii, Toxoplasma gondii, and Mammalian Dihydrofolate Reductase." Pteridines 8, no. 3 (1997): 173–87. http://dx.doi.org/10.1515/pteridines.1997.8.3.173.

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SummaryTen previously undescribed 2,4-diamino-6-(2-naphthylamino )methylpteridines with lipophilic chlorine or long-chain alkyl groups on the naphthyl moiety and either hydrogen or a methyl group on N 10 were synthesized from the appropriate 2-naphthylamine or N-methyl-2-naphthylamine by reaction with 2-amino-5-chloromethylpyrazine-3-carbonitrile and ring closure with guanidine . One analogue with a methyl group at the 7 -position was also prepared. The N 10 -unsubstituted analogues were consistently less active than the N1o-methyl analogues as inhibitors of Pneumocystis carin ii, Toxoplasma g

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14

Kozlov, N. G., A. P. Kadutski, and A. V. Baranovski. "ChemInform Abstract: Condensation of 2-Naphthylamine or N-Benzyl-2-naphthylamines with Formaldehyde and Methyl 2,2-Dimethyl-4,6-dioxocyclohexane-3-carboxylate." ChemInform 44, no. 17 (2013): no. http://dx.doi.org/10.1002/chin.201317155.

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15

Quanfang, Lu, Yu Jie, Gao Jinzhang, and Yang Wu. "Glow Discharge Induced Hydroxyl Radical Degradation of 2-Naphthylamine." Plasma Science and Technology 7, no. 3 (2005): 2856–59. http://dx.doi.org/10.1088/1009-0630/7/3/017.

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16

Kozlov, N. G., L. I. Basalaeva, S. I. Firgang, and A. S. Shashkov. "Reaction of Methylcyclohexanones with Substituted Benzaldehydes and 2-Naphthylamine." Russian Journal of Organic Chemistry 40, no. 4 (2004): 518–24. http://dx.doi.org/10.1023/b:rujo.0000036073.49961.28.

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17

Yenilmez Çiftçi, Gönül, Elif Şenkuytu, Mahmut Durmuş, Fatma Yuksel, and Adem Kılıç. "Structural and fluorescence properties of 2-naphthylamine substituted cyclotriphosphazenes." Inorganica Chimica Acta 423 (November 2014): 489–95. http://dx.doi.org/10.1016/j.ica.2014.09.001.

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18

Bertolotti, S. G., J. J. Cosa, H. E. Gsponer, M. Hamity, and C. M. Previtali. "Electron donor–acceptor complexes between naphthylamines and methyl viologen in aqueous sodium dodecyl sulphate solution." Canadian Journal of Chemistry 64, no. 5 (1986): 845–48. http://dx.doi.org/10.1139/v86-139.

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The electron donor–acceptor (EDA) interaction between methyl viologen (MV2+) and 1-naphthylamine (1NA), 2-naphthylamine (2NA), and N,N-dimethyl-1-naphthylamine (DMA) was studied in water and in aqueous sodium dodecyl sulphate (SDS). The experimental values of the association constants in water were 8.9, 9.8, and 2.8 M−1 for 1NA, 2NA, and DMA, respectively. In the presence of SDS the observed values were very much higher and strongly dependent upon the detergent concentration. The enhancement in the interaction is due to an increase in the local concentration of the partners in the micellar pse

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19

Camargo, H. A., J. A. Henao, D. F. Amado, and V. V. Kouznetsov. "Synthesis and X-ray diffraction data of 1-N-(4-pyridylmethyl)amino naphthalene." Powder Diffraction 25, no. 1 (2010): 72–74. http://dx.doi.org/10.1154/1.3302836.

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1-N-(4-pyridylmethyl)amino naphtalene was synthesized by means of a reaction of alpha-naphthylamine, 4-pyridylcarboxyaldehyde, in anhydrous ethanol to obtainN-(4-pyridylen)-alpha-naphthylamine and that was reduced with NaBH4 to produce the wanted compound. The X-ray powder diffraction pattern for the new compound 1-N-(4-pyrydylmethyl)amino naphtalene was obtained. This compound crystallizes in a monoclinic system with refined unit cell parameters a=10.375(5) Å, b=17.665(6) Å, c=5.566(2) Å, β=100.11(3), and V=1004.3(5) Å3, with space group P2/m (No. 10).

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20

Yang, Li, Fang Wang, Dang-i. Y. Auphedeous, and Chuanliang Feng. "Achiral isomers controlled circularly polarized luminescence in supramolecular hydrogels." Nanoscale 11, no. 30 (2019): 14210–15. http://dx.doi.org/10.1039/c9nr05033g.

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21

Best, WM, BC Mortimer, TG Redgrave, and RV Stick. "The Synthesis of a Fluorescent Cholesteryl Oleate Analogue." Australian Journal of Chemistry 49, no. 11 (1996): 1243. http://dx.doi.org/10.1071/ch9961243.

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A fluorescent analogue of cholesteryl oleate , namely 22-[ethyl(2'-naphthyl)amino]-23,24-dinorchol-5-en-3β-yl oleate, has been prepared from a steroidal carboxylic acid, 2-naphthylamine and oleic acid.

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22

Çiftçi, Gönül Yenilmez, Elif Şenkuytu, Fatma Yuksel, and Adem Kılıç. "Investigation of the structural properties of 2-naphthylamine substituted cyclotetraphosphazenes." Polyhedron 77 (July 2014): 1–9. http://dx.doi.org/10.1016/j.poly.2014.03.062.

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23

Kozlov, N. G., and L. I. Basalaeva. "Cascade heterocyclization of 2-naphthylamine with substituted benzaldehydes and acetophenones." Russian Journal of General Chemistry 76, no. 11 (2006): 1810–16. http://dx.doi.org/10.1134/s1070363206110259.

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24

Orzechowski, Achim, Dieter Schrenk, and Walter Bock. "Metabolism of 1- and 2-naphthylamine in isolated rat hepatocytes." Carcinogenesis 13, no. 12 (1992): 2227–32. http://dx.doi.org/10.1093/carcin/13.12.2227.

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25

Ohe, Tatsuhiko, and Yasuto Watanabe. "Degradation of 2-Naphthylamine-l-sulfonic Acid byPseudomonasStrain TA-1." Agricultural and Biological Chemistry 50, no. 6 (1986): 1419–26. http://dx.doi.org/10.1080/00021369.1986.10867607.

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26

Kozlov, N. G., L. I. Basalaeva, and E. A. Dikusar. "Vanillal Esters in Reaction with 2-Naphthylamine and 1,3-Diketones." Russian Journal of Organic Chemistry 41, no. 11 (2005): 1637–46. http://dx.doi.org/10.1007/s11178-006-0011-2.

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27

Al-Masri, Harbi Tomah. "Synthesis and Molecular Structure of cis-Tetracarbonyl[N-(diphenylphosphino-kP)-naphthalen-1-yl-P,P-diphenylphosphinous amide-kP]chromium(0)." Journal of Crystallography 2014 (March 24, 2014): 1–4. http://dx.doi.org/10.1155/2014/495845.

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The reaction of N,N-bis(diphenylphosphanyl)naphthylamine C10H7-1-N(PPh2)2 with (C5H10NH)2Cr(CO)4 (1 : 1 molar ratio) in dichloromethane afforded cis-[Cr(CO)4{C10H7-1-N(PPh2)2}] (1). This complex was crystallized in the monoclinic space group P21/n. The structure was solved by direct methods and refined by full-matrix least squares techniques to an R factor of 0.0313 for 6488 observed reflections. The Cr-metal is coordinated by four terminal CO molecules and a P,P′-bidentate N,N-bis(diphenylphosphanyl)naphthylamine ligand in a distorted octahedral array. The N-atom adopts a planar geometry with

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28

Luceri, Francesca, Giuseppe Pieraccini, Gloriano Moneti, and Piero Dolara. "Primary Aromatic Amines from Side-Stream Cigarette Smoke are Common Contaminants of Indoor Air." Toxicology and Industrial Health 9, no. 3 (1993): 405–13. http://dx.doi.org/10.1177/074823379300900302.

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A very sensitive mass-spectrometry method has been developed for the analysis of aromatic amines in tobacco smoke and in indoor air. Cigarettes were smoked with a smoking machine; the anwies from the smoke were trapped in a 5% HCl water solution containing internal standards and detected by gas chromatography/mass spectrometry in the selected-ion-monitoring (SIM) mode. The amines measured were the following: aniline. 2-toluidine, 3-toluidine, 4-toluidine, 2-ethylaniline, 3-ethylaniline, 4-ethylaniline, 2,3-dimethylaniline, 2,4-dimethylaniline, 2,5-dimethylaniline, 2,6-dimethylaniline, 1-naphth

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29

Gattu, Radhakrishna, R. Sidick Basha, Prasanta Ray Bagdi, and Abu T. Khan. "One-pot three-component regioselective synthesis of C1-functionalised 3-arylbenzo[f]quinoline." RSC Advances 6, no. 14 (2016): 11675–82. http://dx.doi.org/10.1039/c5ra23413a.

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An efficient method for regioselective synthesis of C1-functionalised 3-arylbenzo[f]quinoline has been demonstrated using β-ketoester, 2-naphthylamine and aromatic aldehyde by employing camphorsulfonic acid as the catalyst in acetonitrile at 70 °C.

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30

Petrikaitė, Vilma, Eduardas Tarasevičius, and Alvydas Pavilonis. "Synthesis and Antimicrobial Properties of Naphthylamine Derivatives Having a Thiazolidinone Moiety." Medicina 47, no. 6 (2011): 47. http://dx.doi.org/10.3390/medicina47060047.

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Objective. The aim of this study was to evaluate the influence of pharmacophores having naphthylamine and nitro groups on the antimicrobial (antibacterial and antifungal) activity of thiazolidinone derivatives. Materials and Methods. The initial 5-substituted-2-methylmercaptothiazolidin-4-ones were subjected to S-demethylation to yield 2-amino-substituted thiazolidinones. 4-Nitro-1-naphthylamine, nitrofuran aldehydes, and nitrobenzene aldehydes were used as pharmacophoric compounds having amino or aldehyde groups. Antimicrobial (antibacterial and antifungal) activity of the new compounds was t

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31

Altenburger, Rolf, Werner Brack, William R. Greco, et al. "On the Mode of Action ofN-Phenyl-2-naphthylamine in Plants." Environmental Science & Technology 40, no. 19 (2006): 6163–69. http://dx.doi.org/10.1021/es060338e.

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32

Ćirić‐Marjanović, G., N. Cvjetićanin, and S. Mentus. "Electrochemical Synthesis and Structure of Poly(2‐methyl‐1‐naphthylamine) Films." Spectroscopy Letters 36, no. 1-2 (2003): 151–65. http://dx.doi.org/10.1081/sl-120021784.

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33

Jia, Run-Hong, Qian-Shang Zhang, Shu-Jiang Tu, and Yan Zhang. "12-(4-Bromophenyl)-9,9-dimethyl-1,2,3,4,9,10-hexahydrobenz[a]acridin-11-one." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): o2032—o2033. http://dx.doi.org/10.1107/s160053680601453x.

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The title compound, C25H22BrNO, has been synthesized by the reaction of 4-bromobenzaldehyde, 3,3-dimethylcyclopentane-1,3-dione with 2-naphthylamine in ethanol. In the crystal structure, the molecules are connected by N—H...O hydrogen bonds, forming chains along the a axis.

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34

Sekar, N. "Substitutes for 1-naphthylamine. Part 1-a comparative study of monoazo anionic dyes from 5-acetaniidoaniline-2-sulphonic acid and 1-naphthylamine." Journal of the Society of Dyers and Colourists 111, no. 12 (2008): 390–93. http://dx.doi.org/10.1111/j.1478-4408.1995.tb01692.x.

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35

Tu, Shu-Jiang, Yan Zhang, and Run-Hong Jia. "11-(4-Fluorophenyl)-7,11-dihydrobenzo[f]furo[3,4-b]quinolin-10(8H)-one." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): o1872—o1873. http://dx.doi.org/10.1107/s160053680601302x.

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The title compound, C21H14FNO2, was synthesized by the reaction of 4-fluorobenzaldehyde, 2-naphthylamine and tetronic acid in water under microwave irradiation. The dihydropyridine ring adopts a flattened boat conformation. N—H...O hydrogen bonds link symmetry-related molecules into a chain along the b axis.

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36

Baker, Robert W., and James A. Taylor. "Synthesis, resolution and rates of racemisation of 1-(2′-methyl-3′-indenyl)-2-naphthylamine and -2-naphthol." Tetrahedron Letters 41, no. 22 (2000): 4471–73. http://dx.doi.org/10.1016/s0040-4039(00)00618-3.

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37

Taldone, Tony, Danuta Zatorska, and Gabriela Chiosis. "Reaction of 2-Naphthylamine with Sodium Iodate/Sodium Sulfite: Synthesis of 2-Amino-1-iodonaphthalene." Synthetic Communications 42, no. 5 (2011): 635–38. http://dx.doi.org/10.1080/00397911.2010.528290.

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38

Kozlov, N. G., K. N. Gusak, and V. V. Skatetskii. "Three-component condensation of 2-naphthylamine with aromatic aldehydes and 5-(2-furyl)-1,3-cyclohexanedione." Russian Journal of Organic Chemistry 42, no. 1 (2006): 112–17. http://dx.doi.org/10.1134/s1070428006010179.

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39

Čeřovský, Václav, Taťána Saks, and Karel Jošt. "Papain-catalyzed synthesis of 2-naphthylamides of N-acylamino acids and dipeptides." Collection of Czechoslovak Chemical Communications 52, no. 9 (1987): 2309–16. http://dx.doi.org/10.1135/cccc19872309.

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2-Naphthylamides of several N-acylamino acids were prepared by papain-catalyzed condensation reaction in acidic medium. Under the same conditions, papain catalyzed the synthesis of peptide bond between benzyloxycarbonylglycine and phenylalanine 2-naphthylamide and between benzyloxycarbonylserine and tyrosine 2-naphthylamide. Phenylalanine 2-naphthylamide was also acylated with benzyloxycarbonyl glycine methyl ester in an alkaline medium. For comparison, papain-catalyzed condensations of benzyloxycarbonyl-S-benzylcysteine or benzyloxycarbonylalanine with aniline and its derivatives, benzylamine

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40

Lei, Wu, Xingen Xie, Qingli Hao, Mingzhu Xia, and Fengyun Wang. "High-quality poly (N-phenyl-2-naphthylamine) films: Electrosynthesis and fluorescent properties." Materials Letters 64, no. 20 (2010): 2211–14. http://dx.doi.org/10.1016/j.matlet.2010.07.045.

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41

OHE, Tatsuhiko, and Yasuto WATANABE. "Degradation of 2-naphthylamine-1-sulfonic acid by Pseudomonas strain TA-1." Agricultural and Biological Chemistry 50, no. 6 (1986): 1419–26. http://dx.doi.org/10.1271/bbb1961.50.1419.

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42

Kozlov, N. G., and K. N. Gusak. "Condensation of 2-naphthylamine with aromatic aldehydes and substituted cyclohexane-1,3-diones." Russian Journal of General Chemistry 76, no. 2 (2006): 278–81. http://dx.doi.org/10.1134/s1070363206020204.

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43

Kozlov, N. G., L. I. Basalaeva, and E. A. Dikusar. "Reaction of Long-Chain Vanillyl Esters with CH-Acids and 2-Naphthylamine." Chemistry of Natural Compounds 40, no. 1 (2004): 79–82. http://dx.doi.org/10.1023/b:conc.0000025473.93772.9e.

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44

Wolska, I., D. Maciejewska, and V. Kowalska. "Solid-state structure of 1-(3′-methylphenylazo)-2-naphthylamine and its acetamide." Acta Crystallographica Section A Foundations of Crystallography 60, a1 (2004): s284. http://dx.doi.org/10.1107/s0108767304094358.

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45

Zhang, Dongchao, Zhiliang Huang, and Aiwen Lei. "Oxidation-induced ortho-selective C–H bond functionalization of 2-naphthylamine derivative." Science China Chemistry 61, no. 10 (2018): 1274–77. http://dx.doi.org/10.1007/s11426-018-9218-5.

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46

Khojasteh-Khosro, Sheida, and Hossein Shahbazi-Alavi. "Preparation of spirooxindoles catalyzed by nano-Co3S4 under microwave irradiations." Journal of Chemical Research 43, no. 3-4 (2019): 107–11. http://dx.doi.org/10.1177/1747519819841791.

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An efficient and rapid method is used for the synthesis of 10-methyl-8 H-spiro[benzo[5,6]chromeno[2,3- c]pyrazole-11,3′-indol]-2′(1′ H)-one and 8-methyl-10-phenyl-10,11-dihydrospiro[pyrazolo[3,4- b]benzo[ h]quinolin-7,3′-indol]-2′(1′ H)-one by a four-component reactions of phenylhydrazine or hydrazine hydrate, isatins, ketoesters, and naphthylamine or 2-naphthol using nano-Co3S4 under microwave irradiation.

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47

Chiang, P. C., and J. S. Wu. "Evaluation of Chemical and Thermal Regeneration of Activated Carbon." Water Science and Technology 21, no. 12 (1989): 1697–700. http://dx.doi.org/10.2166/wst.1989.0147.

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Nine typical aromatic compounds, i.e., Phenol, 2-Aminophenol, Aniline, 2-Chlorophenol, Chlorobenzene, β -Naphthol, Naphthalene, α -Naphthylamine and α -Chioronaphthaiene were introduced to evaluate the effects of the chemical characterization of these selected adsorbates on the desorption efficiency of the activated carbon. Both the thermal and chemical regeneration methods were employed to compare the regeneration efficiencies, operation and maintenance costs among these adsorbates and adsorbent.

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48

Zijp, J. W. H. "Quantitative determination of antioxidants, after a chromatographic separation on completely acetylated filter paper. I. Determination of phenyl-1-naphthylamine and of phenyl-2-naphthylamine." Recueil des Travaux Chimiques des Pays-Bas 76, no. 4 (2010): 313–16. http://dx.doi.org/10.1002/recl.19570760407.

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49

Möhrle, H., and D. Schake. "Heterocyclische Spirocyclohexadienone aus substituierten Phenolen / Heterocyclic Spirocyclohexadienones from Substituted Phenols." Zeitschrift für Naturforschung B 50, no. 12 (1995): 1859–68. http://dx.doi.org/10.1515/znb-1995-1213.

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Mannich bases were prepared from substituted phenols with aliphatic amines and formaldehyde. Amine exchange with N-methyl-2-naphthylamine followed by a Hofmann Martius rearrangement gave rise to o,o′-amino-hydroxy-diphenylmethane derivatives. Under cyclization conditions some of these compounds produced spirocyclohexadienones, which are the ipso analogs to the hypothetic intermediates postulated in the aminomethylation mechanism of phenols.

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Chiang, P. C., E. E. Chang, and J. S. Wu. "Comparison of chemical and thermal regeneration of aromatic compounds on exhausted activated carbon." Water Science and Technology 35, no. 7 (1997): 279–85. http://dx.doi.org/10.2166/wst.1997.0287.

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Abstract:

In this investigation, nine typical compounds, i.e., phenol, 2-aminophenol, aniline, 2-chlorophenol, chlorobenzene, β-naphthol, naphthalene, α-naphthylamine and α-chloronaphthalene were introduced to evaluate the effects of the molecular structure and physicochemical properties of these selected adsorbates on the adsorption capacity and desorption efficiency of the activated carbon. Both the thermal and chemical regeneration methods were employed to compare the regeneration efficiencies among these adsorbates and adsorbent.

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