Статті в журналах з теми "Arylazo"
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Luk'yanov, O. A., T. G. Mel'nikova, and Yu A. Strelenko. "Arylazo- and arylazoxy-N-nitroformamidines." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, no. 5 (May 1991): 997–1002. http://dx.doi.org/10.1007/bf00961362.
Повний текст джерелаLUK'YANOV, O. A., T. G. MEL'NIKOVA, and YU A. STRELENKO. "ChemInform Abstract: Arylazo- and Arylazoxy-N-nitroformamidines." ChemInform 23, no. 50 (September 1, 2010): no. http://dx.doi.org/10.1002/chin.199250140.
Повний текст джерелаDushenko, G. A., I. E. Mikhailov, and V. I. Minkin. "Circumambulatory migrations of arylazo groups in the systems of pentamethoxycarbonyland pentamethylcyclopentadiene." Журнал органической химии 59, no. 9 (September 15, 2023): 1193–208. http://dx.doi.org/10.31857/s0514749223090094.
Повний текст джерелаMijin, Dusan, Gordana Uscumlic, Natasa Valentic, and Aleksandar Marinkovic. "Synthesis of azo pyridone dyes." Chemical Industry 65, no. 5 (2011): 517–32. http://dx.doi.org/10.2298/hemind110428037m.
Повний текст джерелаHeindl, Andreas H., and Hermann A. Wegner. "Starazo triple switches – synthesis of unsymmetrical 1,3,5-tris(arylazo)benzenes." Beilstein Journal of Organic Chemistry 16 (January 3, 2020): 22–31. http://dx.doi.org/10.3762/bjoc.16.4.
Повний текст джерелаDUSHENKO, G. A., I. E. MIKHAILOV, R. V. SKACHKOV, A. A. KLENKIN, L. N. DIVAEVA, and V. I. MINKIN. "ChemInform Abstract: Stable 5-Arylazo-1,2,3,4,5-pentamethoxycarbonylcyclopentadienes - Effective Arylazo Group Transmitter." ChemInform 26, no. 28 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199528084.
Повний текст джерелаElnagdi, Mohamed Hilmy, Nadia Hassen Taha, Fatma Abdel Maksoud Abd El All, Ramadan Maawad Abdel-Motaleb, and Fivian Farouk Mahmoud. "Studies on condensed pyrazoles: Synthesis of new methyl and amino pyrazolo[1,5-a]pyrimidines and of pyrazolo[5,1-c][1,2,4]triazines." Collection of Czechoslovak Chemical Communications 54, no. 4 (1989): 1082–91. http://dx.doi.org/10.1135/cccc19891082.
Повний текст джерелаAl-Azmi, Amal, and Elizabeth John. "Synthesis of 4-arylazo-2-(N-pyrazolylcarboxamido)thiophene disperse dyes for dyeing of polyester and their antibacterial evaluation." Textile Research Journal 90, no. 23-24 (June 9, 2020): 2795–805. http://dx.doi.org/10.1177/0040517520931476.
Повний текст джерелаZayed, Ezzat Mohamed, and Said Ahmed Soliman Ghozlan. "4-AryIazo-3,5-diaminoisoxazoIe: Synthesis and Some Chemical Reactions." Zeitschrift für Naturforschung B 40, no. 12 (December 1, 1985): 1727–30. http://dx.doi.org/10.1515/znb-1985-1222.
Повний текст джерелаBonanno, Nico M., Zackery Watts, Cole Mauws, Brian O. Patrick, Christopher R. Wiebe, Yuki Shibano, Kenji Sugisaki, et al. "Valence tautomerism in a [2 × 2] Co4 grid complex containing a ditopic arylazo ligand." Chemical Communications 57, no. 50 (2021): 6213–16. http://dx.doi.org/10.1039/d1cc01991k.
Повний текст джерелаSinger, Robert D., Keith Vaughan, and Donald L. Hooper. "Open chain nitrogen compounds. Part XI. 3,7-Bis(arylazo)-1,3,5,7-tetraazabicyclo[3,3,1]nonanes: the reaction of diazonium ions with ammonia–formaldehyde mixtures." Canadian Journal of Chemistry 64, no. 8 (August 1, 1986): 1567–72. http://dx.doi.org/10.1139/v86-259.
Повний текст джерелаNitti, Andrea, Angelo Martinelli, Fabrice Batteux, Stefano Protti, Maurizio Fagnoni, and Dario Pasini. "Blue light driven free-radical polymerization using arylazo sulfones as initiators." Polymer Chemistry 12, no. 40 (2021): 5747–51. http://dx.doi.org/10.1039/d1py00928a.
Повний текст джерелаLin, Changxu, Long Yang, Mengchun Xu, Qi An, Zheng Xiang, and Xiangyang Liu. "Properties and applications of designable and photo/redox dual responsive surfactants with the new head group 2-arylazo-imidazolium." RSC Advances 6, no. 57 (2016): 51552–61. http://dx.doi.org/10.1039/c6ra04448d.
Повний текст джерелаWrubel, Jürgen. "3-Arylazo-1, 2-benzisoxazole." Zeitschrift für Chemie 19, no. 12 (August 31, 2010): 452–53. http://dx.doi.org/10.1002/zfch.19790191215.
Повний текст джерелаRen, Demin, Bin Liu, Xiaofang Li, Sebastian Koniarz, Miłosz Pawlicki, and Piotr J. Chmielewski. "Reactions of 2-aza-21-carbaporphyrin with aniline derivatives." Organic Chemistry Frontiers 6, no. 7 (2019): 908–18. http://dx.doi.org/10.1039/c9qo00024k.
Повний текст джерелаAlbini, Angelo, Elisa Fasani, Micaela Moroni, and Silvio Pietra. "Photochemical decomposition of 4-arylazo- and 4-arylazoxy-N,N-dialkylaniline N-oxides." Journal of the Chemical Society, Perkin Transactions 2, no. 9 (1986): 1439. http://dx.doi.org/10.1039/p29860001439.
Повний текст джерелаChawla, Ruchi, Shefali Jaiswal, P. K. Dutta та Lal Dhar S. Yadav. "A photocatalyst-free visible-light-mediated solvent-switchable route to stilbenes/vinyl sulfones from β-nitrostyrenes and arylazo sulfones". Organic & Biomolecular Chemistry 19, № 29 (2021): 6487–92. http://dx.doi.org/10.1039/d1ob01028j.
Повний текст джерелаLuu, Truong Giang, Tien Tan Bui, and Hee-Kwon Kim. "Visible-light-induced one-pot synthesis of sulfonic esters via multicomponent reaction of arylazo sulfones and alcohols." RSC Advances 12, no. 27 (2022): 17499–504. http://dx.doi.org/10.1039/d2ra02656b.
Повний текст джерелаLin, Changxu, Long Yang, Mengchun Xu, Qi An, Zheng Xiang, and Xiangyang Liu. "Correction: Properties and applications of designable and photo/redox dual responsive surfactants with the new head group 2-arylazo-imidazolium." RSC Advances 6, no. 80 (2016): 76453. http://dx.doi.org/10.1039/c6ra90068b.
Повний текст джерелаAlazemi, Abdulrahman M., Kamal M. Dawood, Hamad M. Al-Matar, and Wael M. Tohamy. "Microwave-assisted chemoselective synthesis and photophysical properties of 2-arylazo-biphenyl-4-carboxamides from hydrazonals." RSC Advances 13, no. 36 (2023): 25054–68. http://dx.doi.org/10.1039/d3ra04558g.
Повний текст джерелаAlazemi, Abdulrahman M., Kamal M. Dawood, Hamad M. Al-Matar, and Wael M. Tohamy. "Correction: Microwave-assisted chemoselective synthesis and photophysical properties of 2-arylazo-biphenyl-4-carboxamides from hydrazonals." RSC Advances 13, no. 45 (2023): 31365. http://dx.doi.org/10.1039/d3ra90102e.
Повний текст джерелаLima, Sudhir, Atanu Banerjee, Monalisa Mohanty, Gurunath Sahu, Chahat Kausar, Samir Kumar Patra, Eugenio Garribba, Werner Kaminsky, and Rupam Dinda. "Synthesis, structure and biological evaluation of mixed ligand oxidovanadium(iv) complexes incorporating 2-(arylazo)phenolates." New Journal of Chemistry 43, no. 45 (2019): 17711–25. http://dx.doi.org/10.1039/c9nj01910c.
Повний текст джерелаSinha, Suman, Siuli Das, Rakesh Mondal, Sutanuva Mandal, and Nanda D. Paul. "Cobalt complexes of redox noninnocent azo-aromatic pincers. Isolation, characterization, and application as catalysts for the synthesis of quinazolin-4(3H)-ones." Dalton Transactions 49, no. 25 (2020): 8448–59. http://dx.doi.org/10.1039/d0dt00394h.
Повний текст джерелаRong, Jing, Hao Jiang, Sijing Wang, Zhenni Su, Huiyan Wang, and Chuanzhou Tao. "Metal-free cascade reactions of aziridines with arylalkynes and aryldiazoniums: facile access to arylazopyrrolines." Organic & Biomolecular Chemistry 18, no. 16 (2020): 3149–57. http://dx.doi.org/10.1039/d0ob00346h.
Повний текст джерелаBamoniri, Abdolhamid, and Naimeh Moshtael-Arani. "Nano-Fe3O4 encapsulated-silica supported boron trifluoride as a novel heterogeneous solid acid for solvent-free synthesis of arylazo-1-naphthol derivatives." RSC Advances 5, no. 22 (2015): 16911–20. http://dx.doi.org/10.1039/c4ra12604a.
Повний текст джерелаGstach, H., and J. G. Schantl. "Efficient Synthesis of Arylazo-Methoxy-Diphenylmethanes." Synthetic Communications 16, no. 7 (June 1986): 741–47. http://dx.doi.org/10.1080/00397918608059653.
Повний текст джерелаLi, Ankun, Yuxuan Li, Junjie Liu, Jingqi Chen, Kui Lu, Di Qiu, Maurizio Fagnoni, Stefano Protti, and Xia Zhao. "Metal-Free Trifluoromethylthiolation of Arylazo Sulfones." Journal of Organic Chemistry 86, no. 1 (December 22, 2020): 1292–99. http://dx.doi.org/10.1021/acs.joc.0c02669.
Повний текст джерелаJanecki, Tomasz, Peter L. Pauson, and Antoni Pietrzykowski. "Insertion reactions of 2-(arylazo)aryltricarbonylcobalt." Journal of Organometallic Chemistry 325, no. 1-2 (May 1987): 247–51. http://dx.doi.org/10.1016/0022-328x(87)80404-7.
Повний текст джерелаDUSHENKO, G. A., R. V. SKACHKOV, I. E. MIKHAILOV, L. N. DIVAEVA, and V. I. MINKIN. "ChemInform Abstract: Transfer of the Arylazo Group from 5-Arylazo-1,2,3,4,5- pentamethoxycarbonylcyclopentadienes to Nucleophilic Carbon Centers." ChemInform 26, no. 33 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199533041.
Повний текст джерелаArbabi, Hamidreza Azari, Siavash Salek Soltani, Hasan Salehi, Shahla Rezazadeh, Afsaneh Zonouzi, and Mansoureh Toosibashi. "Convenient Synthesis of Heterocyclic Azo Dyes in the Class of Pyranopyrazoles and Chromenes." Journal of Chemical Research 42, no. 2 (February 2018): 68–72. http://dx.doi.org/10.3184/174751918x15177611816526.
Повний текст джерелаAl-Masoudi, Najim A., Yossra A. Marich, Niran J. Al-Salihi, and Bahjat Saeed. "Synthesis and Modeling Study of Some Potential Pyrimidine Derivatives as HIV Inhibitors." Zeitschrift für Naturforschung B 69, no. 8 (August 1, 2014): 913–23. http://dx.doi.org/10.5560/znb.2014-4107.
Повний текст джерелаAmin, Hawraz I. M., Carlotta Raviola, Ahmed A. Amin, Barbara Mannucci, Stefano Protti, and Maurizio Fagnoni. "Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions." Molecules 24, no. 11 (June 8, 2019): 2164. http://dx.doi.org/10.3390/molecules24112164.
Повний текст джерелаAmrallah, A. H., N. A. Abdalla, and E. Y. El-Haty. "Spectrophotometric Studies on Some Arylazo Barbituric Acids and Arylazo Pyrimidine in Organic Solvents and in Buffer Solutions." Journal of the Chinese Chemical Society 54, no. 6 (December 2007): 1629–37. http://dx.doi.org/10.1002/jccs.200700230.
Повний текст джерелаBlank, Lena, Maurizio Fagnoni, Stefano Protti, and Magnus Rueping. "Visible Light-Promoted Formation of C–B and C–S Bonds under Metal- and Photocatalyst-Free Conditions." Synthesis 51, no. 05 (February 6, 2019): 1243–52. http://dx.doi.org/10.1055/s-0037-1611648.
Повний текст джерелаRaposo, M. Manuela M., Ana M. Ferreira, Michael Belsley, E. de Matos Gomes, and J. C. V. P. Moura. "5-Arylazo-2,2´-Bithiophenes: A Novel Promising Series of NLO Chromophores." Materials Science Forum 587-588 (June 2008): 268–72. http://dx.doi.org/10.4028/www.scientific.net/msf.587-588.268.
Повний текст джерелаYu, Xiuling, Peter Metz, and Horst Hartmann. "A simple route to 2-aryl-substituted naphtho[2,1-e][1,2,4]triazinium and naphtho[2,1-e][1,2,3,4]tetrazinium salts from 1-arylazo-substituted 2-naphthylamines." Zeitschrift für Naturforschung B 73, no. 7 (July 26, 2018): 431–35. http://dx.doi.org/10.1515/znb-2018-0003.
Повний текст джерелаTodres, Zori V., and Ghevork Ts Hovsepyan. "First examples of arylazo derivatives of cyclooctatetraene." Journal of the Chemical Society, Perkin Transactions 1, no. 5 (1997): 747–50. http://dx.doi.org/10.1039/a604933h.
Повний текст джерелаKing, R. Bruce. "Thirty years of organometallic aryldiazenido arylazo derivatives." Journal of Organometallic Chemistry 500, no. 1-2 (September 1995): 187–94. http://dx.doi.org/10.1016/0022-328x(95)00504-j.
Повний текст джерелаRusakov, Yury Yu, Leonid B. Krivdin, Elena Yu Senotrusova, Elena Yu Schmidt, Alexander M. Vasiltsov, Albina I. Mikhaleva, Boris A. Trofimov, Oleg A. Dyachenko, Anatolii N. Chekhlov, and Olga N. Kazheva. "Conformational study of 2-arylazo-1-vinylpyrroles." Magnetic Resonance in Chemistry 45, no. 2 (2007): 142–51. http://dx.doi.org/10.1002/mrc.1934.
Повний текст джерелаRazus, Alexandru C., Liviu Birzan, Stefan A. Razus, and Viorica Horga. "ChemInform Abstract: Halogenation of 1-Arylazo-azulenes." ChemInform 31, no. 37 (September 12, 2000): no. http://dx.doi.org/10.1002/chin.200037058.
Повний текст джерелаShmalko, Akim V., Sergei A. Anufriev, Marina Yu Stogniy, Kyrill Yu Suponitsky, and Igor B. Sivaev. "Synthesis and structure of 3-arylazo derivatives of ortho-carborane." New Journal of Chemistry 44, no. 25 (2020): 10199–202. http://dx.doi.org/10.1039/d0nj02052d.
Повний текст джерелаTuck, Jeremy R., Robert J. Tombari, Noah Yardeny, and David E. Olson. "A Modular Approach to Arylazo-1,2,3-triazole Photoswitches." Organic Letters 23, no. 11 (May 21, 2021): 4305–10. http://dx.doi.org/10.1021/acs.orglett.1c01230.
Повний текст джерелаSchulze, Margit, and Horst Hartmann. "PREPARATION AND CHARACTERIZATION OF 1-ARYLAZO-SUBSTITUTED NAPHTHYLSULFIDES." Phosphorus, Sulfur, and Silicon and the Related Elements 61, no. 1-2 (August 1991): 161–71. http://dx.doi.org/10.1080/10426509108027349.
Повний текст джерелаRustler, Karin, Philipp Nitschke, Sophie Zahnbrecher, Julia Zach, Stefano Crespi, and Burkhard König. "Photochromic Evaluation of 3(5)-Arylazo-1H-pyrazoles." Journal of Organic Chemistry 85, no. 6 (February 19, 2020): 4079–88. http://dx.doi.org/10.1021/acs.joc.9b03097.
Повний текст джерелаPorobić, Slavica J., Aleksandar D. Krstić, Dragana J. Jovanović, Jelena M. Lađarević, Đurica B. Katnić, Dušan Ž. Mijin, and Milena Marinović-Cincović. "Synthesis and thermal properties of arylazo pyridone dyes." Dyes and Pigments 170 (November 2019): 107602. http://dx.doi.org/10.1016/j.dyepig.2019.107602.
Повний текст джерелаRajagopal, R., and S. Seshadri. "Synthesis and study of 6-arylazo coumarin derivatives." Dyes and Pigments 13, no. 1 (January 1990): 29–44. http://dx.doi.org/10.1016/0143-7208(90)80011-d.
Повний текст джерела., M. Sreedevi Meesaraganda, and Raghavendra Guru Prasad Aluru . "SYNTHESIS AND ANTIMICROBIAL EVALUATION OF CERTAIN ARYLAZO IMIDAZOLES." Journal of Applied Pharmacy 5 (July 1, 2013): 100–106. http://dx.doi.org/10.21065/19204159.5.100.
Повний текст джерелаAbd-El-Aziz, Alaa S., Rawda M. Okasha, Patrick O. Shipman, and Tarek H. Afifi. "Neutral and Cationic Cyclopentadienyliron Macromolecules Containing Arylazo Chromophores." Macromolecular Rapid Communications 25, no. 16 (August 26, 2004): 1497–503. http://dx.doi.org/10.1002/marc.200400218.
Повний текст джерелаBulgakova, N. A., L. M. Gornostaev, V. T. Sakilidi, and V. A. Loskutov. "ChemInform Abstract: Amination of 1-Arylazo-4-chloroanthraquinones." ChemInform 33, no. 22 (May 21, 2010): no. http://dx.doi.org/10.1002/chin.200222111.
Повний текст джерелаKamigata, Nobumasa, Mayumi Satoh, Masato Yoshida, Yoshihiro Nakamura, Koichi Kikuchi, and Isao Ikemoto. "NOVEL REACTION OF ARYLAZO ARYL AND ARYLAZOXY ARYL SULFONES WITH NORBORNENE CATALYZED BY A PALLADIUM(0) COMPLEX." Phosphorus, Sulfur, and Silicon and the Related Elements 69, no. 1-2 (June 1992): 129–36. http://dx.doi.org/10.1080/10426509208036861.
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