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Journal articles on the topic 'N-phenyl'

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Published: 18 May 2024

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1

Ajibade, Peter A., Benjamin C. Ejelonu, and Bernard Omondi. "N-Ethyl-N-phenyl{[ethyl(phenyl)carbamothioyl]disulfanyl}carbothioamide." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (June 23, 2012): o2182. http://dx.doi.org/10.1107/s1600536812027808.

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2

Shen, Heng-Shui, Nan Liu, Zi-Cheng Li, and Wen-Cai Huang. "N-Ethyl-N-phenyl-N′-tosylformamidine." Acta Crystallographica Section E Structure Reports Online 65, no. 7 (June 17, 2009): o1582. http://dx.doi.org/10.1107/s1600536809021953.

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3

Fu, T. Y., J. R. Scheffer, and J. Trotter. "N-Phenyl-N-(phenylthioxomethyl)benzamide." Acta Crystallographica Section C Crystal Structure Communications 54, no. 1 (January 15, 1998): 101–2. http://dx.doi.org/10.1107/s0108270197011244.

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4

Dou, Shi-qi, B. Thimme Gowda, Helmut Paulus, and Alarich Weiss. "The Bond N-Cl. Crystal Structures and 35Cl NQR of N-Chloro-N-Phenyl-2-chloroacetamide, N-Chloro-N-phenyl-2,2-dichloroacetamide, N-Chloro-N-phenyl-2,2,2-trichloroacetamide, and N-Phenyl-2,2,2-trichloroacetamide." Zeitschrift für Naturforschung A 49, no. 12 (December 1, 1994): 1136–44. http://dx.doi.org/10.1515/zna-1994-1206.

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Abstract The crystal structures of C6H5NClCOCH2Cl (1), C6H5NClCOCHCl2 (2), C6H5NClCOCCl3 (3),and C6H5NHCOCCl3 (4) have been determined at room temperature (lattice constants, d in pm).(1): P21 /c, Z = 4, a = 738, b = 645, c = 1891, β = 90.41°, d (N -C l) = 171, d (C = O ) = 121; (2): P21 /c, Z = 4, a = 820, b = 1495, c = 905, β = 114.78°, d (N -Cl) = 171, d (C = O ) = 120; (3): P 21/c, Z = 4,a = 819, b = 1853, c = 718, β = 103.64°, d (N -Cl) = 172, d (C = O ) = 120; (4): P21/c, Z = 4, a = 551, b = 1704, c = 1035, β = 93.08°, d (C = O) = 121.For (2), (3), and (4) the 35Cl NQR frequencies have been determined in the range 77 ≤ T /K ≤ 300. At 77 K (γ in MHz): (2): γ(w,1) = 37.600, γ(w,2) = 38.188, γ(N) = 51.858; (3): γ(w,1) = 39.944, γ(w,2) = 40.512, γ(w,3) = 40.739, γ(N) = 52.791; (4): γ(w,1) = 39.428, γ(w,2) = 39.452, γ(w,3) = 39.986. For the compound C6H5NHCOCHCl2 (5) the 35Cl NQ R measured at 77 K is: γ(w,1) = 37.195 MHz, γ(w,2) = 37.596 MHz. The relation, γ(35Cl) = d (N -Cl) is discussed.

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5

Han, Li-Ping, Bin Li, Jie Liu, and Qing-Chun Liu. "N-Phenyl-N-{4-[5-(2-phenyl-3-pyridyl)-1,3,4-oxadiazol-2-yl]phenyl}aniline." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (November 21, 2007): o4780. http://dx.doi.org/10.1107/s1600536807058382.

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6

Young Chang, Ji, Tae Ja Kim, Man Jung Han, and Kyu Ho Chae. "Polymerization of N-[4-(azidocarbonyl)phenyl]maleimide and N-[4-(N′-phenoxycarbonylamino)phenyl]maleimide." Polymer 40, no. 14 (June 1999): 4049–54. http://dx.doi.org/10.1016/s0032-3861(98)00600-4.

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7

Özçelik, Suzan, Muharrem Dinçer, Memet Şekerci, Ayla Balaban, and Ümmühan Özdemir. "N-Phenyl-N′-(2-thienylmethylene)hydrazine." Acta Crystallographica Section E Structure Reports Online 60, no. 9 (August 21, 2004): o1552—o1553. http://dx.doi.org/10.1107/s1600536804019932.

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8

Fu, T. Y., J. R. Scheffer, and J. Trotter. "N-Phenyl-N-(phenylthioxomethyl)benzamide. Erratum." Acta Crystallographica Section C Crystal Structure Communications 54, no. 4 (April 15, 1998): 562. http://dx.doi.org/10.1107/s0108270198003357.

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9

Mo, Shanyan. "N-Cyano-N-phenyl-p-toluenesulfonamide." Synlett 25, no. 09 (April 11, 2014): 1337–38. http://dx.doi.org/10.1055/s-0033-1341246.

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10

Khan, Islam Ullah, Mehmet Akkurt, Faiza Anwar, and Shahzad Sharif. "N-[4-(N-Cyclohexylsulfamoyl)phenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (March 20, 2010): o868—o869. http://dx.doi.org/10.1107/s160053681000961x.

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11

Khan, Islam Ullah, Zeeshan Haider, Muhammad Nadeem Arshad, and Sharafat Ali. "N-Ethyl-N-phenyl-p-toluenesulfonamide." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (March 31, 2010): o979. http://dx.doi.org/10.1107/s1600536810011219.

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12

Hoque, Md Ehtesham Ul, and Hai-Whang Lee. "Pyridinolysis of Phenyl N-Phenyl Phosphoramidochloridate in Acetonitrile." Bulletin of the Korean Chemical Society 33, no. 10 (October 20, 2012): 3437–40. http://dx.doi.org/10.5012/bkcs.2012.33.10.3437.

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13

PARKIN, JUDITH, NICK P. TOMKINSON, and RICHARD VIRDEN. "Inhibition of chymotrypsin by phenyl N-phenyl-phosphoramidochloridate." Biochemical Society Transactions 20, no. 3 (August 1, 1992): 283S. http://dx.doi.org/10.1042/bst020283s.

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14

Datta, Mritunjoy, Alan J. Buglass, and Mark R. J. Elsegood. "N-Phenyl-tert-butanesulfinamide." Acta Crystallographica Section E Structure Reports Online 65, no. 8 (July 29, 2009): o2034. http://dx.doi.org/10.1107/s1600536809028633.

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15

Yu, Da-sheng, Fang-shi Li, Wei Yao, Yin-hong Liu, and Chui Lu. "N,N-Dimethyl-N′-[3-(trifluoromethyl)phenyl]urea." Acta Crystallographica Section E Structure Reports Online 64, no. 7 (June 7, 2008): o1220. http://dx.doi.org/10.1107/s1600536808016656.

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16

Capella, Laura, Antonella Capperucci, Giovanni Curotto, Dario Lazzari, Pasquale Dembech, Gianna Reginato, and Alfredo Ricci. "Silylcupration of N-phenyl-N-ethynyl-aniline: A versatile route to functionalized N,N-bis(phenyl)enamines." Tetrahedron Letters 34, no. 20 (May 1993): 3311–14. http://dx.doi.org/10.1016/s0040-4039(00)73691-4.

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17

Ajibade, Peter A., and Damian C. Onwudiwe. "Synthesis and characterization of group 12 complexes of N,N-methyl phenyl-N,N-butyl phenyl dithiocarbamate." Journal of Coordination Chemistry 64, no. 17 (August 19, 2011): 2963–73. http://dx.doi.org/10.1080/00958972.2011.606906.

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18

Gataullin, Rail R., Ivan S. Afon’kin, Akhnaf A. Fatykhov, Leonid V. Spirikhin, and Il’dus B. Abdrakhmanov. "Iodocyclization of N-(2-nitrophenyl)- and N-phenyl-N’-[2-(alk-1-enyl)phenyl]ethanimidamides." Mendeleev Communications 11, no. 5 (January 2001): 201–2. http://dx.doi.org/10.1070/mc2001v011n05abeh001490.

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19

Kühnau, Hans-Hellmut, and Horst-Robert Schütte. "Synthesen radioaktiv markierter Verbindungen; Synthese von N-Phenyl-N'-dimethylharnstoff(Fenuron)-[Phenyl-14C] und N-Phenyl-N'-dimethylharnstoff(Fenuron)-[14CH3] bzw. N-(p-Chlorphenyl)-N'-dimethylharnstoff(Monuron-[14CH3]." Zeitschrift für Chemie 9, no. 6 (September 1, 2010): 231–32. http://dx.doi.org/10.1002/zfch.19690090609.

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20

Han, Li-Ping, Bin Li, and Jie Liu. "N-Phenyl-N-{4-[5-(4-pyridyl)-1,3,4-oxadiazol-2-yl]phenyl}aniline." Acta Crystallographica Section E Structure Reports Online 64, no. 1 (December 12, 2007): o242. http://dx.doi.org/10.1107/s1600536807065245.

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21

Wang, Zhi-Qiang, Rui Zhang, Xiao-Juan Sun, Ya-Peng Zhang, Yan Xu, and Chen Xu. "Crystal structure of N-phenyl-N-(4-(pyren-1- yl)phenyl)benzenamine, C34H23N." Zeitschrift für Kristallographie - New Crystal Structures 225, no. 3 (September 2010): 573–74. http://dx.doi.org/10.1524/ncrs.2010.0251.

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22

Chopra, Deepak, A. R. Choudhury, K. Nagarajan, and T. N. Guru Row. "N-Phenylethyl-N'-[3-(trifluoromethyl)phenyl]thiourea." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (October 9, 2004): o1970—o1971. http://dx.doi.org/10.1107/s1600536804024961.

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23

Manjare, Sudesh T., Ray J. Butcher, and Harkesh B. Singh. "N-[2-(2-Bromobenzylamino)phenyl]-N-butylformamide." Acta Crystallographica Section E Structure Reports Online 65, no. 11 (October 23, 2009): o2826. http://dx.doi.org/10.1107/s1600536809042883.

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24

Pavia, Michael R., Sandra J. Lobbestael, Charles P. Taylor, Fred M. Hershenson, and David L. Miskell. "N-Phenyl-N'-pyridinylureas as anticonvulsant agents." Journal of Medicinal Chemistry 33, no. 2 (February 1990): 854–61. http://dx.doi.org/10.1021/jm00164a061.

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25

Fun, Hoong-Kun, Chin Wei Ooi, Dinesha, S. Viveka, and G. K. Nagaraja. "(Z)-N-[2-(N′-Hydroxycarbamimidoyl)phenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 69, no. 3 (February 9, 2013): o370—o371. http://dx.doi.org/10.1107/s1600536813003371.

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26

Podkopaeva, O. Y., D. L. Kuznetsov, V. D. Belov, and Y. V. Chizhov. "Electronic structure of phenyl-N,N-dimorpholinomethanes." Journal of Structural Chemistry 41, no. 4 (July 2000): 616–25. http://dx.doi.org/10.1007/bf02683924.

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27

CAPELLA, L., A. CAPPERUCCI, G. CUROTTO, D. LAZZARI, P. DEMBECH, G. REGINATO, and A. RICCI. "ChemInform Abstract: Silylcupration of N-Phenyl-N-ethynylaniline: A Versatile Route to Functionalized N,N-Bis(phenyl)enamines." ChemInform 24, no. 41 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199341145.

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28

Shadab, Mohd, and Mohammad Aslam. "Synthesis and Characterization of Some Transition Metal complexes with N-phenyl-N’-[substituted phenyl] Thiourea." Material Science Research India 11, no. 1 (August 30, 2014): 83–89. http://dx.doi.org/10.13005/msri/110111.

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A series of thiourea ligand , N-N'- diphenyl thiourea [I] [DPTH], N-phenyl-N'-[2-phenoyl] thiourea [II] [PPTH], N-phenyl-N'-[2-chlorophenyl] thiourea III [PCPTH], N-phenyl-N'- [5-chloro-2-methyl phenyl] thiourea IV [PCMPTH] and N- phenyl -N'-(5-chloro-2-methoxy phenyl) thiourea V (PCMTPTH) and their transition metal complexes of the type ML2 and ML2 Cl2 have been synthesized by reacting phenyl isothiocyanate with substituted aniline and transition metal salts. These newly synthesized ligands and their complexes were characterized by elemental and spectral studies. Based upon these studies it was revealed that in all the cases metal is coordinated through suphur group of thioamide of ligands. In case of nickel complexes, the nickel is coordinated to both oxygen and sulphur. In all the complexes metal is tetra coordinated forming a square planer geometry.

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29

Dikic, Branko, Stephen G. Pyne, Brian W. Skelton, and Allan H. White. "(2 R *, S S *)- N -Phenyl- N -(2-N′- Tert -Butyldiphenylsilyl- S -Phenylsulfonimidoyl-1-Phenyl)Ethylamine." Sulfur Letters 25, no. 2 (January 1, 2002): 63–66. http://dx.doi.org/10.1080/02786110211432.

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30

Albores-Velasco, Martha, John Thorne, and Ralph L. Wain. "Fungicidal activity of phenyl N-(4-substituted-phenyl)thionocarbamates." Journal of Agricultural and Food Chemistry 43, no. 8 (August 1995): 2260–61. http://dx.doi.org/10.1021/jf00056a054.

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31

Fortin, Sébastien, Emmanuel Moreau, Jacques Lacroix, Jean-Claude Teulade, Alexandre Patenaude, and René C-Gaudreault. "N-Phenyl-N′-(2-chloroethyl)urea analogues of combretastatin A-4: Is the N-phenyl-N′-(2-chloroethyl)urea pharmacophore mimicking the trimethoxy phenyl moiety?" Bioorganic & Medicinal Chemistry Letters 17, no. 7 (April 2007): 2000–2004. http://dx.doi.org/10.1016/j.bmcl.2007.01.023.

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32

Percino, Teresa Mancilla, Roxana Magaly Flores Ancona, and Marisol López Martínez. "New strategy to the synthesis of (N→B) phenyl[N-alkyliminodiacetate-O,O′,N]boranes: The crystal structure of (N→B) phenyl[N-benzyliminodiacetate-O,O′,N]borane, (N→B)phenyl[N-(4-methyl)benzyliminodiacetate-O,O′,N]borane and (N→B) phenyl[N-phenacyliminodiacetate-O,O′,N]borane." Polyhedron 28, no. 13 (September 2009): 2771–75. http://dx.doi.org/10.1016/j.poly.2009.05.043.

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33

Muruganandam, L., S. Rajeswari, D. Tamilvendan, V. Ramkumar, and G. Venkatesa Prabhu. "N-[Morpholino(phenyl)methyl]benzamide." Acta Crystallographica Section E Structure Reports Online 65, no. 3 (February 21, 2009): o578. http://dx.doi.org/10.1107/s1600536809005327.

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34

Yin, Guodong, Shengli Hu, Yitao Li, and Anxin Wu. "N-[4-(Phenylethynyl)phenyl]benzamide." Acta Crystallographica Section E Structure Reports Online 61, no. 8 (July 16, 2005): o2561—o2562. http://dx.doi.org/10.1107/s1600536805022105.

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35

Chin, Taylor, Frank R. Fronczek, and Ralph Isovitsch. "N-[4-(Morpholinodiazenyl)phenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 65, no. 12 (November 25, 2009): o3206. http://dx.doi.org/10.1107/s160053680904937x.

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36

Sun, Xiaofei, Xiaoping Zhang, Binbin Zhang, Wenguo Wang, and Qingle Zeng. "(S)-N-Phenyl-tert-butanesulfinamide." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (May 16, 2012): o1728. http://dx.doi.org/10.1107/s1600536812020673.

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The asymmetric unit of the title compound, C10H15NOS, contains two independent molecules with similar conformations. In the crystal, molecules are linked in a head-to-tail fashion by N—H...O hydrogen bonds into chains running along the b axis. The absolute configuration was assigned on the basis of known chirality of the parent compound.

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37

Rehman, Jeveria, Ejaz, Islam Ullah Khan, William T. A. Harrison, and Sidra Farid. "N-[4-(Ethylsulfamoyl)phenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (August 27, 2011): o2455. http://dx.doi.org/10.1107/s1600536811033472.

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38

Ahmad, Saba, Muhammad Akhyar Farrukh, Fahim Ashraf Qureshi, Islam Ullah Khan, and Mehmet Akkurt. "N-[4-(Propylsulfamoyl)phenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (January 7, 2012): o290—o291. http://dx.doi.org/10.1107/s1600536811055528.

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39

John, Peter, Waqar Ahmad, Islam Ullah Khan, Shahzad Sharif, and Edward R. T. Tiekink. "N-[4-(Benzylsulfamoyl)phenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 66, no. 8 (July 17, 2010): o2048. http://dx.doi.org/10.1107/s1600536810027698.

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40

Zhang, Wen-Jie, Jian-Xin Chen, Zhong-Shui Li, Ai-Ke Li, and Xin-Rong Lin. "N-[2-(Diphenylphosphino)phenyl]benzamide." Acta Crystallographica Section E Structure Reports Online 63, no. 10 (September 15, 2007): o4016. http://dx.doi.org/10.1107/s1600536807042092.

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41

Decken, Andreas, Johanna M. Blacquiere, Christopher M. Vogels, and Stephen A. Westcott. "N-[(Benzylcarbamoyl)(phenyl)methyl]-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzamide." Acta Crystallographica Section E Structure Reports Online 62, no. 6 (May 10, 2006): o2207—o2208. http://dx.doi.org/10.1107/s1600536806016126.

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42

Kawski, Alfons, Barbara Bartoszewicz, and Cerylia Strzalkowska. "Elektrische Dipolmomente von N-Phenyl-α-naphthylamin und N-Phenyl-β-naphthylamin im Anregungszustand." Zeitschrift für Chemie 12, no. 7 (September 1, 2010): 275. http://dx.doi.org/10.1002/zfch.19720120719.

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43

Li, Xin-Gui, Mei-Rong Huang, Zhi-Liang Zhu, Yi Jin, and Xue-Song Wang. "Structure and thermal degradation of poly(N-phenyl acrylamide) and poly(N-phenyl methacrylamide)." Journal of Applied Polymer Science 88, no. 4 (February 14, 2003): 1065–71. http://dx.doi.org/10.1002/app.11824.

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44

Hoffmann, Siegfried, Nguyen Thi Hanh, Kerstin Mandl, Gerald Brezesinski, and Eckhard Günther. "Vinamid-Mesogene - [4-n-Alkoxy-phenyl]-[β-(4-n-alkoxy-phenyl)amino-vinyl]-ketone." Zeitschrift für Chemie 26, no. 3 (August 31, 2010): 103–4. http://dx.doi.org/10.1002/zfch.19860260312.

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45

Gataullin, Rail R., Ivan S. Afon'kin, Akhnaf A. Fatykhov, Leonid V. Spirikhin, and Il'dus B. Abdrakhmanov. "ChemInform Abstract: Iodocyclization of N-(2-Nitrophenyl)- and N-Phenyl-N′-[2-(alk-1-enyl)phenyl]ethanimidamides." ChemInform 33, no. 11 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200211037.

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46

Basenko, S. V., L. E. Zelenkov, M. G. Voronkov, and A. I. Albanov. "Phenyl(trimethylsiloxy)fluorosiloxanes PhSi(OSiMe3) n F3−n." Russian Journal of General Chemistry 79, no. 6 (June 2009): 1083–85. http://dx.doi.org/10.1134/s1070363209060073.

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47

Pang, Tao, Yi-chong Sun, and Jian-ming Zhang. "N-Phenyl-N-(3-phenylprop-2-ynyl)aniline." Acta Crystallographica Section E Structure Reports Online 65, no. 10 (September 26, 2009): o2555. http://dx.doi.org/10.1107/s1600536809037866.

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48

Yusof, Mohd Sukeri Mohd, Nur Farhana Embong, Suhana Arshad, and Ibrahim Abdul Razak. "N-(4-Chlorobutanoyl)-N′-[2-(trifluoromethyl)phenyl]thiourea." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (March 10, 2012): o1029. http://dx.doi.org/10.1107/s1600536812008859.

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In the title compound, C12H12ClF3N2OS, the dihedral angle between the benzene ring and the thiourea fragment is 69.41 (5)°. The thiourea N—H atoms adopt ananticonformation, such that one of them forms an intramolecular N—H...O hydrogen bond, generating anS(6) ring. In the crystal, both N—H groups form inversion dimers, oneviaa pair of N—H...S hydrogen bonds and oneviaa pair of N—H...O hydrogen bonds. These lead toR22(8) andR22(12) loops, respectively. Weak C—H...Cl, C—H...F, C—H...S and π–π [centroid–centroid separation = 3.7098 (6)Å and slippage = 1.853 Å] interactions also occur.

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49

Miyamoto, Hisakazu, Genta Yamauchi, Takuya Ueno, and Hidehiro Uekusa. "Crystal structure of N-isopropyl-N-(phenyl)phenylglyoxylamide." Acta Crystallographica Section E Crystallographic Communications 74, no. 11 (October 12, 2018): 1574–76. http://dx.doi.org/10.1107/s2056989018013762.

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The title compound [systematic name: 2-oxo-N,2-diphenyl-N-(propan-2-yl)acetamide], C17H17NO2, was synthesized and its photoreactive properties in the crystalline state were investigated. In the molecule, the carbonyl group attached to the phenyl ring adopts an s-trans configuration with respect to the isopropyl group. Moreover, the distance between the C atom of the carbonyl group and the N-bound C atom of the isopropyl group is 3.845 (2) Å, which is much longer than 3.2 Å, the threshold for photoreactions to take place in the molecule. As a result, the crystal did not photoreact upon UV light irradiation. In the crystal, the molecules are linked via weak intermolecular C—H...O hydrogen bonds, forming a layer structure parallel to the ab plane.

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50

Yuan, Chunlan. "N-(2,4-Dinitrophenyl)-N′-[nitro(phenyl)methylene]hydrazine." Acta Crystallographica Section E Structure Reports Online 64, no. 12 (November 8, 2008): o2297. http://dx.doi.org/10.1107/s1600536808036179.

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