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Journal articles on the topic '2-aryl-2'

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Published: 4 June 2021
Last updated: 26 July 2025

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1

Burchardt, Annette, and Detlef Geffken. "N-Substituierte 2-Aryl-2-hydroxycarbohydroxamsäuren N-Substituted 2-Aryl-2-hydroxy-carbohydroxamic Acids." Archiv der Pharmazie 323, no. 3 (1990): 181–83. http://dx.doi.org/10.1002/ardp.19903230310.

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2

LEHNERT, W. "3-Aryl-2-nitropropansäure-ester aus 3-Aryl-2-nitro-2-propensäure-estern." Synthesis 1976, no. 12 (2002): 827–29. http://dx.doi.org/10.1055/s-1976-24226.

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3

Feigenbaum, Alexandre, Yves Fort, Jean Pierre Pete, and Denise Scholler. "Photochemical cyclization of 2-alkyl-3-aryl-2-cyclohexenones and 2-alkoxy-3-aryl-2-cyclohexenones." Journal of Organic Chemistry 51, no. 23 (1986): 4424–32. http://dx.doi.org/10.1021/jo00373a015.

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4

Kashima, Choji, and Hideki Arao. "Synthesis of 2-Aryl- and 5-Alkyl-2-aryloxazoles from 2-Aryl-5-bromooxazoles." Synthesis 1989, no. 11 (1989): 873–74. http://dx.doi.org/10.1055/s-1989-27419.

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5

Matiichuk, Yuliia, Yuri Gorak, Roman Martyak, et al. "Synthesis and antimicrobial activity of 4-(5-ARYL-2-FUROYL)morpholines and 4-[(5-ARYL-2-FURYL)carbonothioyl] morpholines." Pharmacia 68, no. (1) (2021): 175–79. https://doi.org/10.3897/pharmacia.68.e46942.

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By the reaction of furan-2-carboxylic acids and furfural with diazonium salts 1a-j the arylfuran-2-carboxylic acids 4a-e and 5-arylfuran-2-carbaldehydes 5a-f were synthesized. Acids 4a-e were transformed into appropriated acylchlorides 6a-e and were used for preparation of 4-(5-aryl-2-furoyl)morpholines 7a-e. 4-[(5-Aryl-2-furyl)carbonothioyl]morpholines 8a-f were prepared from aldehydes 5a-f by using Willgerodt-Kindler reaction. The structures of the obtained compounds were confirmed by <sup>1</sup>H NMR spectroscopy and elemental analysis. All these new compounds gave spectroscopic data in ac
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6

Cativiela, C., M. P. López, and J. A. Mayoral. "Synthesis of 2-Aryl-2-methylglycine Derivatives." Synlett 1992, no. 02 (1992): 121–22. http://dx.doi.org/10.1055/s-1992-21285.

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7

TODA, Kazuya, Masuo GOTO, Yasuo KIKUCHI, et al. "Synthesis and Herbicidal Activity of N-Aryl-2-methyl-2-aryipropanamides and N-Aryl-2-methyl-2-arylbutanamides." Journal of Pesticide Science 13, no. 1 (1988): 19–27. http://dx.doi.org/10.1584/jpestics.13.19.

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8

Ciganek, Engelbert. "2-(Methoxymethyl)--3-aryl-2-propenoic Acids and 2-(Bromomethyl)-3-aryl-2-propenoic Acids from Aromatic Aldehydes." Journal of Organic Chemistry 60, no. 14 (1995): 4635–37. http://dx.doi.org/10.1021/jo00119a047.

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9

Kolyamshin, O. A., and V. A. Danilov. "N-Aryl-2-dialkylaminosuccinimides." Russian Journal of Organic Chemistry 40, no. 7 (2004): 982–85. http://dx.doi.org/10.1023/b:rujo.0000045189.81688.f3.

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10

Kovalev, Vladimir V., Andrey K. Rozov, and Elvira A. Shokova<. "Stereoselective Isomerisation of 2-Aryl-2-hydroxyadamantanes: A Convenient Method for (Z)-2-Aryl-5-hydroxyadamantanes." Synlett 1990, no. 12 (1990): 739–40. http://dx.doi.org/10.1055/s-1990-21232.

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11

Bhatt, Divya, Pratibha Kalaramna, Krishn Kumar, and Avijit Goswami. "Chemoselective RuII -Catalyzed Synthesis of Aryl Thiocyanates and Step-wise Double [2+2+2] Cycloadditions to 2-Aryl Thiopyridines." European Journal of Organic Chemistry 2020, no. 29 (2020): 4606–11. http://dx.doi.org/10.1002/ejoc.202000691.

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12

Corsaro, Antonino, Antonio Corsaro, and Giovanni Puglisi. "A Convenient Synthesis of 2-Aryl- and 2-Arylamino-4-aryl-5-cyanothiazoles." HETEROCYCLES 23, no. 10 (1985): 2645. http://dx.doi.org/10.3987/r-1985-10-2645.

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13

Clark, Andrew J., Stuart R. Coles, Alana Collis, David R. Fullaway, Nicholas P. Murphy, and Paul Wilson. "2-Aryl propionamides via 1,4-aryl radical migration from N-arylsulfonyl-2-bromopropionamides." Tetrahedron Letters 50, no. 46 (2009): 6311–14. http://dx.doi.org/10.1016/j.tetlet.2009.08.125.

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14

Paponov, B. V., O. V. Shishkin, S. V. Shishkina, R. I. Zubatyuk, A. L. Kalyuzhny, and V. I. Musatov. "Dimerization of 3-(2-aryl-2-oxoethylidene)oxindoles." Russian Chemical Bulletin 57, no. 3 (2008): 622–31. http://dx.doi.org/10.1007/s11172-008-0098-4.

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15

Abdelaal, Salma M., Jang-Woo Kim, and Ludwig Bauer. "Synthesis of aryl 2-(2-imidazolyl)ethyl ketones." Journal of Heterocyclic Chemistry 32, no. 3 (1995): 903–6. http://dx.doi.org/10.1002/jhet.5570320338.

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16

Lin, Shaw-Tao, Mei-Ling Lin, and Wen-Chung Lin. "Mass spectra of 1-aryl-2, 2-dibromocyclopropanes." Organic Mass Spectrometry 25, no. 12 (1990): 667–70. http://dx.doi.org/10.1002/oms.1210251208.

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17

Tao, Bin, and David W. Boykin. "Pd(OAc)2/2-aryl-2-oxazolines catalyzed Suzuki coupling reactions of aryl bromides and arylboronic acids." Tetrahedron Letters 43, no. 28 (2002): 4955–57. http://dx.doi.org/10.1016/s0040-4039(02)00955-3.

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18

Ali, Omar M. "Synthesis of N 2-Arylisocytidines and N 2-Aryl-2′-deoxyisocytidines." Monatshefte für Chemie - Chemical Monthly 138, no. 9 (2007): 917–22. http://dx.doi.org/10.1007/s00706-007-0671-9.

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19

Mollet, Karen, Matthias D’hooghe, and Norbert De Kimpe. "Transformation oftrans-4-Aryl-3-chloro-1-(2-chloroethyl)azetidin-2-ones into 3-Aryl-2-(ethylamino)propan-1-ols via Intermediate 1-(1-Aryl-2-chloro-3-hydroxypropyl)aziridines andtrans-2-Aryl-3-(hydroxymethyl)aziridines." Journal of Organic Chemistry 76, no. 1 (2011): 264–69. http://dx.doi.org/10.1021/jo1020932.

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20

Mohr, Lisa-Marie, Andreas Bauer, Christian Jandl, and Thorsten Bach. "Visible light-mediated intermolecular [2 + 2] photocycloaddition of 1-aryl-2-nitroethenes and olefins." Organic & Biomolecular Chemistry 17, no. 30 (2019): 7192–203. http://dx.doi.org/10.1039/c9ob01146c.

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21

Kakanejadifard, Ali, Toraj Hayati, and Azam Rezayat. "Synthesis and Characterization of New Schiff Bases 2-(2-(2-(Aryl)Methyleneamino)Phenylthio) Ethylthio)-N-((aryl)Methylene)Benzeneamine." Phosphorus, Sulfur, and Silicon and the Related Elements 185, no. 7 (2010): 1511–15. http://dx.doi.org/10.1080/10426500903107930.

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22

Özdemir, Ahmet, Gülhan Turan-Zitouni, Zafer Asım Kaplancıklı, Gilbert Revial, and Kıymet Güven. "Synthesis and antimicrobial activity of 1-(4-aryl-2-thiazolyl)-3-(2-thienyl)-5-aryl-2-pyrazoline derivatives." European Journal of Medicinal Chemistry 42, no. 3 (2007): 403–9. http://dx.doi.org/10.1016/j.ejmech.2006.10.001.

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23

Alekseenko, T. A., T. S. Bazhbeuk-Melikova, O. V. Zelenskaya, and V. A. Kozinskii. "2-Aryl-1,2,3-thiadiazolium salts." Chemistry of Heterocyclic Compounds 25, no. 11 (1989): 1299–300. http://dx.doi.org/10.1007/bf00481528.

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24

Hedrick, J. L., and R. Twieg. "Imide-aryl ether phenylquinoxalines 2." Polymer 38, no. 4 (1997): 995–99. http://dx.doi.org/10.1016/s0032-3861(96)00701-x.

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25

Augustin, Manfred, and Manfred Köhler. "Synthese von 2-Aryl-maleinimiden." Zeitschrift für Chemie 15, no. 3 (2010): 102. http://dx.doi.org/10.1002/zfch.19750150306.

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26

Pei, Weiwei, Shaohui Li, Xiaoping Nie, et al. "Convenient Syntheses of 2-Alkyl(Aryl)-4,5-diphenyloxazoles and 2-Alkyl(Aryl)-4-phenyloxazoles." Synthesis 1998, no. 09 (1998): 1298–304. http://dx.doi.org/10.1055/s-1998-6093.

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27

Geden, Joanna V., Alpa K. Pancholi, and Michael Shipman. "Palladium-Catalyzed Multicomponent Synthesis of 2-Aryl-2-imidazolines from Aryl Halides and Diamines." Journal of Organic Chemistry 78, no. 8 (2013): 4158–64. http://dx.doi.org/10.1021/jo400252n.

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28

Verniest, Guido, Sven Claessens, Filip Bombeke, Tinneke Van Thienen, and Norbert De Kimpe. "Synthesis of 2-aryl-4-chloropyrroles via ring expansion of 2-aryl-1-chlorocyclopropanecarbaldehydes." Tetrahedron 61, no. 11 (2005): 2879–87. http://dx.doi.org/10.1016/j.tet.2005.01.087.

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29

Bertolini, Ferruccio, Stefano Crotti, Valeria Di Bussolo, Franco Macchia, and Mauro Pineschi. "Regio- and Stereoselective Ring Opening of Enantiomerically Enriched 2-Aryl Oxetanes and 2-Aryl Azetidines with Aryl Borates." Journal of Organic Chemistry 73, no. 22 (2008): 8998–9007. http://dx.doi.org/10.1021/jo801568a.

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30

Fadeev, Alexander A., Alexey O. Chagarovskiy, Anton S. Makarov, et al. "Synthesis of (Het)aryl 2-(2-hydroxyaryl)cyclopropyl Ketones." Molecules 25, no. 23 (2020): 5748. http://dx.doi.org/10.3390/molecules25235748.

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A simple general method for the synthesis of 1-acyl-2-(ortho-hydroxyaryl)cyclopropanes, which belong to the donor–acceptor cyclopropane family, has been developed. This method, based on the Corey–Chaykovsky cyclopropanation of 2-hydroxychalcones, allows for the preparation of a large diversity of hydroxy-substituted cyclopropanes, which can serve as promising building blocks for the synthesis of various bioactive compounds.
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31

Xu, Hongyu, and Li Jia. "Novel Cobalt-Catalyzed Carbonylation of 2-Aryl-2-oxazolines." Organic Letters 5, no. 9 (2003): 1575–77. http://dx.doi.org/10.1021/ol034380f.

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32

Shono, Tatsuya, Naoki Kise, Ryoji Nomura, and Ayuko Yamanami. "Reductive homo-coupling of 2-aryl-2-oxazolinium salts." Tetrahedron Letters 34, no. 22 (1993): 3577–80. http://dx.doi.org/10.1016/s0040-4039(00)73640-9.

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33

Chow, Ken, and Harold W. Moore. "(2-Aryl-2-cyanoethenyl)ketenes---annulated cyanophenols from azidoquinones." Tetrahedron Letters 28, no. 42 (1987): 5013–16. http://dx.doi.org/10.1016/s0040-4039(00)96683-8.

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34

Benneche, Tore, and Marcus A. Tius. "Synthesis of 2-oxaadamantane and 1-aryl-2-oxaadamantanes." Tetrahedron Letters 57, no. 29 (2016): 3150–51. http://dx.doi.org/10.1016/j.tetlet.2016.06.027.

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35

Guirado, Antonio, Raquel Andreu, Jesús Gálvez, and Peter G. Jones. "Electrochemical generation of 4-amino-2-aryl-2-oxazolines." Tetrahedron 58, no. 49 (2002): 9853–58. http://dx.doi.org/10.1016/s0040-4020(02)01288-7.

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36

Brown, Kenneth L., Orrin Perkins, Zoltan Szeverenyi, and Annamaria Fulep-Poszmik. "Synthesis, characterization and decomposition of 2-aryl-2-hydroxyethylcobaloximes." Journal of Organometallic Chemistry 302, no. 1 (1986): 101–15. http://dx.doi.org/10.1016/0022-328x(86)80065-1.

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37

Liu, Kwang-Ting, and Mann-Yan Kuo. "Solvolysis of 2-aryl-3,3-dimethyl-2-butyl -nitrobensoates." Tetrahedron 44, no. 12 (1988): 3523–30. http://dx.doi.org/10.1016/s0040-4020(01)85982-2.

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38

Dotsenko, V. V., E. A. Chigorina, and S. G. Krivokolysko. "N-Hydroxymethylation of 3-Aryl-2-cyanoprop-2-enethioamides." Russian Journal of General Chemistry 90, no. 8 (2020): 1411–17. http://dx.doi.org/10.1134/s107036322008006x.

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39

Chavan, Subhash P., Krishna S. Ethiraj, and Subhash K. Kamat. "Facile synthesis of 2Z-2-Chloromethyl aryl-2-enoates." Tetrahedron Letters 38, no. 42 (1997): 7415–16. http://dx.doi.org/10.1016/s0040-4039(97)01744-9.

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40

CATIVIELA, C., M. P. LOPEZ, and J. A. MAYORAL. "ChemInform Abstract: Synthesis of 2-Aryl-2-methylglycine Derivatives." ChemInform 23, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.199235265.

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41

Han Lee, In-Sook, Eun Ji Jeoung, and Chang Kiu Lee. "Synthesis and NMR Studies of (E)-1-Aryl-3-(2-pyrrolyl)-2-propenones and (E)-3-Aryl-1-(2-pyrrolyl)-2-propenones." Bulletin of the Korean Chemical Society 34, no. 3 (2013): 936–42. http://dx.doi.org/10.5012/bkcs.2013.34.3.936.

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42

Shchepin, V. V., Yu G. Stepanyan, P. S. Silaichev, M. A. Ezhikova, and M. I. Kodess. "Cyclopropanation of 2-arylmethylidenemalononitriles, alkyl 3-aryl-2-cyanoprop-2-enoates, and N-substituted 3-aryl-2-cyanoprop-2-enamides with bromine-containing zinc enolates." Russian Journal of Organic Chemistry 43, no. 7 (2007): 1002–7. http://dx.doi.org/10.1134/s1070428007070111.

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43

Davies, Stephen G., Timothy J. Donohoe, and M. Anne Lister. "Asymmetric synthesis of 2-aryl-tetrahydropyrans via arene chromium tricarbonyl methodology 2: 2-Aryl-3-ethyl-4-chloro-tetrahydropyrans." Tetrahedron: Asymmetry 2, no. 11 (1991): 1089–92. http://dx.doi.org/10.1016/s0957-4166(00)82003-0.

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44

de Jong, M. H., and W. H. Laarhoven. "Conformational preference of cis-1-aryl-2-(2-benzo[C]phenanthryl)-and cis-1-aryl-2-(3-phenanthryl)-ethenes." Recueil des Travaux Chimiques des Pays-Bas 92, no. 6 (2010): 673–82. http://dx.doi.org/10.1002/recl.19730920615.

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45

Tao, Bin, and David W. Boykin. "ChemInform Abstract: Pd(OAc)2/2-Aryl-2-oxazolines Catalyzed Suzuki Coupling Reactions of Aryl Bromides and Arylboronic Acids." ChemInform 33, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.200241100.

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46

Ryabukhin, Sergey V., Andrey S. Plaskon, Anton V. Tverdokhlebov, and Andrey A. Tolmachev. "2‐Benzothiazolemethanol as Precursor of 2‐Aryl‐1‐(2‐benzothiazolyl)‐1‐ethanones." Synthetic Communications 34, no. 8 (2004): 1483–87. http://dx.doi.org/10.1081/scc-120030699.

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47

V., S. JOLLY, та P. SHARMA K. "Studies on Aryl Thiosemicarbazones and 2-Oxo- Δ 2-thiazolin-2-ylhydrazones". Journal of Indian Chemical Society Vol. 67, May 1990 (1990): 412–13. https://doi.org/10.5281/zenodo.6164698.

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Chemical Laboratories, Government Model Science College, Gwalior-474 011 <em>Manuscript received 22 September 1989, accepted 6 December 1989</em> A number of aryl thiosemicarbazones and 4-oxo-&Delta;<sup>2</sup>-thiazolin-2-ylhydrazones have been synthesised and tested for <em>in vitro </em>activity against <em>M. tuberculosis </em>(H<sub>37&nbsp;</sub>Rv) and antiviral activity for AIDS.
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48

M., N. JOSHI, S. BHAGWAT V., S. BHAGWAT V., and A. PARVATE J. "Synthesis of 3-[ 4" -Aryl-(2" -4' -bithiazol)-2' -yl]-2-aryl- 5-carboxymethyl-4-thiazolidinones and their Ester Derivatives." Journal of Indian Chemical Society Vol. 70, Jun 1993 (1993): 607–8. https://doi.org/10.5281/zenodo.5918084.

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Chemistry Department. Parle College, Dixit Road, Vile Parle (East), Bombay-400 057 <em>Manuscript received 4 December 1992, accepted 8 February 1993</em> Synthesis of 3-[ 4&quot; -Aryl-(2&quot; -4&#39; -bithiazol)-2&#39; -yl]-2-aryl- 5-carboxymethyl-4-thiazolidinones and their Ester Derivatives
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49

Okamura, Mutsuo, Ken Hazama, Mie Ohta, Keiko Kato, Takaaki Horaguchi, and Atsuyoshi Ohno. "Exalted Resonance Effect in the Aryl-Assisted Solvolyses of 2-Aryl-2-(trifluoromethyl)ethylm-Nitrobenzenesulfonates." Chemistry Letters 26, no. 10 (1997): 973–74. http://dx.doi.org/10.1246/cl.1997.973.

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50

Phillion, Dennis P., and John K. Pratt. "A New Method for Hydrolyzing 2-Aryl-4,4-Dimethyl-2-Oxazolines to Aryl Carboxylic Acids." Synthetic Communications 22, no. 1 (1992): 13–22. http://dx.doi.org/10.1080/00397919208021074.

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