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Journal articles on the topic 'Phenylthioureas'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Kaválek, Jaromír, Josef Jirman, and Vojeslav Štěrba. "Kinetics and mechanism of rearrangement and methanolysis of acylphenylthioureas." Collection of Czechoslovak Chemical Communications 50, no. 3 (1985): 766–78. http://dx.doi.org/10.1135/cccc19850766.

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S-Acyl-1-phenylthioureas and their 3-methyl derivatives are rearranged to 1-acyl derivatives of thiourea in methanolic solution. The rearrangement of the 1-acyl-1-phenyl derivative to the thermodynamically more stable 3-acyl derivative is subject to specific base catalysis. The rearrangement of acetyl group is about 2 orders of magnitude slower than that of benzoyl group. 1-Acetyl-l-phenylthiourea undergoes base-catalyzed methanolysis (giving phenylthiourea and methyl acetate) instead of the rearrangement. The methanolysis rates of l-acyl-3-phenylthioureas and their N-methyl derivatives have b

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2

B., H. Zaware, A. Mane R., and B. Ingle D. "Kinetics of reaction of chloroacetone with thioureas." Journal of Indian Chemical Society Vol. 77, Apr 2000 (2000): 213–14. https://doi.org/10.5281/zenodo.5867060.

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Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431 004, India <em>Manuscript received 20 July 1998, revised 16 August 1999, accepted 26 November 1999</em> The second order rate constants for the reactions of chloroacetone with thiourea, phenylthiourea and p-substituted phenylthioureas have been evaluated in ethanol medium. The rate of reaction is first order with respect to chloroacetone and first order with respect to thioureas. The effect of substituents on the rate of reaction is also studied. Thermodynamic parameters are used to explain the nature of reac

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3

Tanimori, Shinji, Asuka Fuchiya, Takuya Miyamura, et al. "A Facile Synthesis of 2-Aminobenzoxazines Based on IodineCatalyzed Desulfurative Cyclization." Synthesis 54, no. 02 (2021): 483–89. http://dx.doi.org/10.1055/s-0040-1719832.

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AbstractA facile and environmentally benign access to N-aryl/alkyl-4H-benzoxazin-2-amines is achieved from 1-[2-(hydroxymethyl)phenyl/alkyl]-3-phenylthioureas under transition-metal-free conditions. The conversions occur smoothly in the presence of a catalytic amount of molecular iodine and hydrogen peroxide as the oxidant in tetrahydrofuran at room temperature to afford moderate to good yields (28–90%) of the desired products within 2 hours. This method reports the first examples of the catalytic transformations of 1-[2-(hydroxymethyl)phenyl/alkyl]-3-phenylthioureas into N-aryl/alkyl-4H-benzo

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4

Tanimori, Shinji, Asuka Fuchiya, Takuya Miyamura, et al. "A Facile Synthesis of 2-Aminobenzoxazines Based on IodineCatalyzed Desulfurative Cyclization." Synthesis 54, no. 02 (2021): 483–89. http://dx.doi.org/10.1055/s-0040-1719832.

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AbstractA facile and environmentally benign access to N-aryl/alkyl-4H-benzoxazin-2-amines is achieved from 1-[2-(hydroxymethyl)phenyl/alkyl]-3-phenylthioureas under transition-metal-free conditions. The conversions occur smoothly in the presence of a catalytic amount of molecular iodine and hydrogen peroxide as the oxidant in tetrahydrofuran at room temperature to afford moderate to good yields (28–90%) of the desired products within 2 hours. This method reports the first examples of the catalytic transformations of 1-[2-(hydroxymethyl)phenyl/alkyl]-3-phenylthioureas into N-aryl/alkyl-4H-benzo

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5

Spooner, Michael J., and Philip A. Gale. "Anion transport across varying lipid membranes – the effect of lipophilicity." Chemical Communications 51, no. 23 (2015): 4883–86. http://dx.doi.org/10.1039/c5cc00823a.

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6

Qian, Xuhong, Zhibin Li, Gonghua Song, and Zhong Li. "Yellow HgO as an efficient Cyclodesulfurising agent in the Synthesis of 2-substituted Aminobenzoxazoles from N-(2-hydroxyphenyl)-N′-phenylthioureas." Journal of Chemical Research 2001, no. 4 (2001): 138–39. http://dx.doi.org/10.3184/030823401103169441.

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7

Srikrishna, Devulapally, and Pramod Kumar Dubey. "PEG-600 mediated one-pot reaction of 3-acetyl-2H-chromen-2-one with heterylthiols and phenylthioureas using tetrabutylammonium tribromide as an efficient green reagent." New Journal of Chemistry 41, no. 12 (2017): 5168–75. http://dx.doi.org/10.1039/c7nj00504k.

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A simple method for the one-pot reaction of 3-acetyl-2H-chromen-2-one with different heterylthiols and phenylthioureas under green conditions using tetrabutylammonium tribromide (TBATB) as an efficient reagent has been described.

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8

Macías, A., A. Rosado, and E. Otazo. "Pyrolysis of 1-furoyl-3-phenylthioureas in mass spectrometry." Journal of Analytical and Applied Pyrolysis 38, no. 1-2 (1996): 55–60. http://dx.doi.org/10.1016/s0165-2370(96)00949-7.

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9

Coppola, Gary M., Robert E. Damon, J. Bruce Eskesen, Dennis S. France, and James R. Paterniti. "1-Hydroxyalkyl-3-phenylthioureas as novel HDL-elevating agents." Bioorganic & Medicinal Chemistry Letters 15, no. 3 (2005): 809–12. http://dx.doi.org/10.1016/j.bmcl.2004.10.094.

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10

Kaválek, Jaromír, Josef Jirman, Vladimír Macháček, and Vojeslav Štěrba. "The methanolysis kinetics and dissociation constants of 1-(subst. benzoyl)-3-phenylthioureas." Collection of Czechoslovak Chemical Communications 53, no. 3 (1988): 593–600. http://dx.doi.org/10.1135/cccc19880593.

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A series of seven 1-(subst. benzoyl)-3-phenylthioureas have been prepared and their dissociation constants and solvolysis rate constants have been measured in methanol at 25 °C. The reaction constants found show that the solvolysis rate is limited by the attack of methoxide ion on the benzoyl carbonyl group of the non-dissociated substrate. The polar effect of substituents in benzoyl group is extensively transferred also by the intramolecular hydrogen bond.

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11

Brown, Ainka T., and Nadale K. Downer-Riley. "A Green Approach to 2-Substituted Benzo- and Naphthothiazoles via N-bromosuccinimide/Bromide-Mediated C(aryl)-S Bond Formation." Molecules 27, no. 22 (2022): 7876. http://dx.doi.org/10.3390/molecules27227876.

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2-Substituted benzo- and naphthothiazoles have been conveniently prepared from the intramolecular cyclization of phenylthioureas and activated thiobenzanilides or the coupling of isothiocyanates with amines under mild conditions using N-bromosuccinimide/tetrabutylammonium bromide in 1,2-dimethoxyethane (DME) under ambient conditions. The reactions produce moderate to excellent yields with good functional group tolerance and avoid the use of harsh thermal conditions, corrosive reagents, halogenated solvents, toxic metal salts, and expensive metal catalysts, and are amenable to preparations on a

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12

Wozniak, Krzysztof, Iwona Wawer, and Dieter Stroehl. "Structural Similarities and Differences between N-Phenylureas and N-Phenylthioureas." Journal of Physical Chemistry 99, no. 21 (1995): 8888–95. http://dx.doi.org/10.1021/j100021a065.

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13

Kim, Taek Hyeon, Jung Ki Min, and Gue-Jae Lee. "One-pot synthesis of 2-phenylaminothiazolines from N-2-hydroxyethyl)-N′-phenylthioureas." Tetrahedron Letters 40, no. 47 (1999): 8201–4. http://dx.doi.org/10.1016/s0040-4039(99)01704-9.

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14

Unkovskii, B. V., I. P. Boiko, Yu F. Malina, T. D. Sokolova, V. F. Shchegel'skii, and L. N. Knyaz'kova. "Synthesis of 5,6-dihydro-4h-1,3-thiazines based on substituted n-phenylthioureas." Chemistry of Heterocyclic Compounds 28, no. 10 (1992): 1225–28. http://dx.doi.org/10.1007/bf00529593.

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15

Valdés-Martı́nez, Jesús, Simón Hernández-Ortega, Georgina Espinosa-Pérez, et al. "Structural, spectral and thermal studies of substituted N-(2-pyridyl)-N′-phenylthioureas." Journal of Molecular Structure 608, no. 1 (2002): 77–87. http://dx.doi.org/10.1016/s0022-2860(01)00934-6.

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16

Na, Hye-Sun, and Taek-Hyeon Kim. "2-Phenylamino-2-oxazolines from N-(2-Hydroxyethyl)-N-phenylthioureas using TsCl/NaOH." Journal of the Korean Chemical Society 47, no. 6 (2003): 671–74. http://dx.doi.org/10.5012/jkcs.2003.47.6.671.

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17

Bai, Lin, Shengying Li, Jin-Xian Wang, and Mingkai Chen. "SYNTHESIS OF BENZOYL-N-PHENYLTHIOUREAS UNDER MICROWAVE IRRADIATION AND PHASE TRANSFER CATALYSIS CONDITIONS." Synthetic Communications 32, no. 1 (2002): 127–32. http://dx.doi.org/10.1081/scc-120001519.

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18

UNKOVSKII, B. V., I. P. BOIKO, YU F. MALINA, T. D. SOKOLOVA, V. F. SHCHEGEL'SKII, and L. N. KNYAZ'KOVA. "ChemInform Abstract: Synthesis of 5,6-Dihydro-4H-1,3-thiazines from Substituted N- Phenylthioureas." ChemInform 24, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199346186.

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19

Coppola, Gary M., Robert E. Damon, J. Bruce Eskesen, Dennis S. France, and James R. Paterniti. "Biological evaluation of 1-alkyl-3-phenylthioureas as orally active HDL-elevating agents." Bioorganic & Medicinal Chemistry Letters 16, no. 1 (2006): 113–17. http://dx.doi.org/10.1016/j.bmcl.2005.09.034.

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20

Glotova, Tatýana, Nadezhda Protsuk, Alexander Albanov, Valentin Lopyrev, and Gennadii Dolgushin. "Dithiobiuretes in reactions with electrophilic acetylenes. New derivatives of 1,3,5-dithiazines,-thiadiazines and-triazines as the products of competing reactions of nucleophilic cycloaddition." Open Chemistry 1, no. 3 (2003): 222–32. http://dx.doi.org/10.2478/bf02476225.

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AbstractThe nucleophilic addition of 2,4-dithiobiurete, 1- and 1,4-substituted 2,4-dithiobiuretes (2 a-e) with benzoylacetylene (1) has been studied. 2-(Benzoylmethyl)-4-(R1-imino)-6-(R2-imino)dihydro-4H-1,3,5-dithiazinium perchlorates (3 a-e) are obtained in glacial acetic acid (AcOH) in the presence of equimolar quantities of HClO4. The reaction of benzoylacetylene with 1,5-diphenyl-2,4-dithiobiurete in either of MeOH, C6H6, or MeCN solvents proceeds non-selectively to give a mixture of products such as 2-(benzoylmethyl)-4,6-di(phenylimino)dihydro-4H-1,3,5-dithiazine (5), 2-(benzoylmethyl)-4

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21

Avetisyan, K. S., and L. Kh Galstyan. "Alkylation of 5,5-Substituted N-[4-Methyl-3-phenylfuran-2(5H)-ylidene]-N′-phenylthioureas." Russian Journal of Organic Chemistry 55, no. 7 (2019): 974–77. http://dx.doi.org/10.1134/s1070428019070091.

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22

RANISE, A., F. BONDAVALLI, O. BRUNO, et al. "ChemInform Abstract: 3,3-Disubstituted 1-Acyl-1-phenylthioureas with Platelet Antiaggregation and Other Activities." ChemInform 22, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199144160.

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23

Kim, Taek Hyeon, Jung Ki Min, and Gue-Jae Lee. "ChemInform Abstract: One-Pot Synthesis of 2-Phenylaminothiazolines from N-(2-Hydroxyethyl)-N′-phenylthioureas." ChemInform 31, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.200005139.

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24

Ares, Jeffrey J., Thomas G. Urchek, Charles W. Palmer, and Duane D. Miller. "Comparison of the thiocarbonyl13C NMR resonances ofN-phenylthioureas,N-phenyl thiocarbamates andN-phenyl dithiocarbamates." Magnetic Resonance in Chemistry 24, no. 5 (1986): 460–61. http://dx.doi.org/10.1002/mrc.1260240513.

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25

Ning, Yonggong, Hong Xie, Huting Xing, Wenli Deng, and Daben Yang. "Comparison of Self-Assembled Monolayers ofn-Alkanethiols and Phenylthioureas on the Surface of Gold." Surface and Interface Analysis 24, no. 9 (1996): 667–70. http://dx.doi.org/10.1002/(sici)1096-9918(19960916)24:9<667::aid-sia158>3.0.co;2-p.

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26

Kim, Taek Hyeon, Jung Ki Min, and Gue-Jae Lee. "Corrigendum to “One-pot synthesis of 2-phenylamino-thiazolines from N-(2-hydroxyethyl)-N′-phenylthioureas”." Tetrahedron Letters 42, no. 12 (2001): 2413. http://dx.doi.org/10.1016/s0040-4039(01)00133-2.

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27

Bai, Lin, Shengying Li, Jin-Xian Wang, and Mingkai Chen. "ChemInform Abstract: Synthesis of Benzoyl-N-phenylthioureas under Microwave Irradiation and Phase Transfer Catalysis Conditions." ChemInform 33, no. 24 (2010): no. http://dx.doi.org/10.1002/chin.200224104.

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28

Zhang, Youming, Jingdong Qin, Qi Lin, and Taibao Wei. "Convenient synthesis and anion recognition properties of N-flurobenzoyl-N′-phenylthioureas in water-containing media." Journal of Fluorine Chemistry 127, no. 9 (2006): 1222–27. http://dx.doi.org/10.1016/j.jfluchem.2006.06.018.

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29

Avetisyan, K. S., L. Kh Galstyan, R. A. Tamazyan, and A. G. Aivazyan. "Synthesis and Structure of 5,5-Disubstituted N-[4-Methyl-3-phenylfuran-2(5H)-ylidene]-N′-phenylthioureas." Russian Journal of Organic Chemistry 54, no. 7 (2018): 1109–11. http://dx.doi.org/10.1134/s1070428018070242.

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30

Kim, Taek Hyeon, Jung Ki Min, and Gue-Jae Lee. "ChemInform Abstract: Ring Closure of N-(2-Hydroxyethyl)-N′-phenylthioureas: One-Pot Synthesis of 2-Phenylaminothiazolines." ChemInform 32, no. 12 (2001): no. http://dx.doi.org/10.1002/chin.200112133.

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31

Kim, Taek Hyeon, Namgun Lee, Gue-Jae Lee, and Jae Nyoung Kim. "A mild cyclodesulfurization of N-(2-hydroxyethyl)-N′-phenylthioureas to 2-phenylamino-2-oxazolines using TsCl/NaOH." Tetrahedron 57, no. 33 (2001): 7137–41. http://dx.doi.org/10.1016/s0040-4020(01)00682-2.

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32

Chang, Hae Sung, Gyu Hwan Yon, and Yong Hae Kim. "Facile Synthesis of 2-Substituted Aminobenzoxazole. One Pot Cyclodesulfurization ofN-(2-Hydroxyphenyl)-N′-phenylthioureas with Superoxide Radical Anion." Chemistry Letters 15, no. 8 (1986): 1291–94. http://dx.doi.org/10.1246/cl.1986.1291.

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33

Thanigaimalai, P., Tuan Anh Le Hoang, Ki-Cheul Lee, et al. "Structural requirement(s) of N-phenylthioureas and benzaldehyde thiosemicarbazones as inhibitors of melanogenesis in melanoma B 16 cells." Bioorganic & Medicinal Chemistry Letters 20, no. 9 (2010): 2991–93. http://dx.doi.org/10.1016/j.bmcl.2010.02.067.

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34

West, Douglas X., Collin P. Galloway, Catherine A. Paulson, Roger K. Bunting, and Lewis K. Pannell. "Cobalt(II) halide complexes ofN-2-(4-picolyl)-,N-2-(6-picolyl)-andN-2-(4,6-lutidyl)-N?-phenylthioureas." Transition Metal Chemistry 14, no. 6 (1989): 420–24. http://dx.doi.org/10.1007/bf01092582.

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35

Lee, Gue-Jae, Jae Nyoung Kim, and Taek Hyeon Kim. "ChemInform Abstract: Investigation of the Cyclization of N-(2-Hydroxyethyl)-N′-phenylthioureas: Mitsunobu Conditions vs TsCl/NaOH System." ChemInform 33, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.200228057.

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36

Kim, Taek Hyeon, Namgun Lee, Gue-Jae Lee, and Jae Nyoung Kim. "ChemInform Abstract: A Mild Cyclodesulfurization of N-(2-Hydroxyethyl)-N′-phenylthioureas to 2-Phenylamino-2-oxazolines Using TsCl/NaOH." ChemInform 32, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200150113.

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37

Sahasrabuddhey, Bhushan, Archana Jain, and Krishna K. Verma. "Determination of ammonia and aliphatic amines in environmental aqueous samples utilizing pre-column derivatization to their phenylthioureas and high performance liquid chromatography." Analyst 124, no. 7 (1999): 1017–21. http://dx.doi.org/10.1039/a902587a.

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38

Qian, Xuhong, Zhibin Li, Gonghua Song, and Zhong Li. "ChemInform Abstract: Yellow HgO as an Efficient Cyclodesulfurizing Agent in the Synthesis of 2-Substituted Aminobenzoxazoles (II) from N-(2-Hydroxyphenyl)-N′-phenylthioureas (I)." ChemInform 32, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.200138122.

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39

D. Kesuma, Siswandono, and A. Kirtishanti. "MOLECULAR DOCKING AND BIOLOGICAL ACTIVITY OF N- (4-METHOXY)-BENZOYL-N’-PHENYLTHIOUREA AND N-(4- TRIFLUORO)-BENZOYL-N’-PHENYLTHIOUREA AS ANTIBREAST CANCER CANDIDATES." RASAYAN Journal of Chemistry 15, no. 02 (2022): 1503–8. http://dx.doi.org/10.31788/rjc.2022.1526836.

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Current breast cancer therapy does not always work optimally, and cases of resistance have been reported. Therefore, it is imperative to develop new effective drugs with minimal side effects through predictions of the epidermal growth factor receptor (EGFR) signalling pathway inhibition. Among chemicals with the potential as anticancer candidates for breast cancer are phenylthiourea derivatives. In this study, two phenylthiourea derivatives were synthesized: N- (4-methoxy)-benzoyl-N'-phenylthiourea and N-(4-trifluoromethyl)-benzoyl-N'-phenylthiourea. These compounds were docked with the EGFR r

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40

Shen, Yi-Hong, and Duan-Jun Xu. "Phenylthiourea." Acta Crystallographica Section E Structure Reports Online 60, no. 7 (2004): o1193—o1194. http://dx.doi.org/10.1107/s1600536804013947.

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41

Kesuma, Dini, Aguslina Kirtishanti, Citra H. A. Makayasa, and I. Gede A. Sumartha. "Anticancer activity of N-(4-t-butylbenzoyl)-N’-phenylthiourea: Molecular docking, synthesis, and cytotoxic activity in breast and cervical cancer cells." Journal of Pharmacy & Pharmacognosy Research 11, no. 2 (2023): 208–15. http://dx.doi.org/10.56499/jppres22.1508_11.2.208.

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Context: N-(4-t-butylbenzoyl)-N’-phenylthiourea, a derivative compound of N-benzoyl-N’-phenylthiourea, has relatively high lipophilicity with the epidermal growth factor receptor and silent mating type information regulation-1 enzyme as its molecular targets. Aims: To determine the anticancer activity of N-(4-t-butylbenzoyl)-N’-phenylthiourea as an in silico and in vitro anticancer candidate for the breast and cervical cancer. Methods: In silico test was performed to predict the cytotoxic activity using AutoDock Vina. This activity was also measured in vitro using the Microculture Tetrazolium

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42

Rahman, Faizan Ur, Maryam Bibi, Ezzat Khan, et al. "Thiourea Derivatives, Simple in Structure but Efficient Enzyme Inhibitors and Mercury Sensors." Molecules 26, no. 15 (2021): 4506. http://dx.doi.org/10.3390/molecules26154506.

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In this study six unsymmetrical thiourea derivatives, 1-isobutyl-3-cyclohexylthiourea (1), 1-tert-butyl-3-cyclohexylthiourea (2), 1-(3-chlorophenyl)-3-cyclohexylthiourea (3), 1-(1,1-dibutyl)-3-phenylthiourea (4), 1-(2-chlorophenyl)-3-phenylthiourea (5) and 1-(4-chlorophenyl)-3-phenylthiourea (6) were obtained in the laboratory under aerobic conditions. Compounds 3 and 4 are crystalline and their structure was determined for their single crystal. Compounds 3 is monoclinic system with space group P21/n while compound 4 is trigonal, space group R3:H. Compounds (1–6) were tested for their anti-cho

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43

Jayabaskaran, C., and K. Ramalingam. "Characterization of phenol oxidase in a pseudophyllidean cestode Penetrocephalus ganapatii." Parasitology 90, no. 3 (1985): 433–40. http://dx.doi.org/10.1017/s0031182000055426.

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The biochemical characteristics of phenol oxidase obtained from Penetrocephalus ganapatii have been investigated using manometric and electrophoretic techniques. Phenol oxidase was found to have maximum activity at pH 7·4, the Michaelis constant for dopamine was 189 μM and the enzyme was stable between 20 and 40°C. Potassium cyanide, sodium diethyldithiocarbamate and phenylthiourea strongly suppressed enzyme activity. The Ki values for potassium cyanide, diethyldithiocarbamate and phenylthiourea were 33μM, 700 μM and 938 μM respectively. The properties of soluble and insoluble enzymes to vario

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44

Yusof, M. Sukeri M., Siti 'Afifah Tunnur M. Asrab, and Bohari M. Yamin. "N-Cyclohexylcarbonyl-N′-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (2007): o4627. http://dx.doi.org/10.1107/s1600536807055079.

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45

Yamin, Bohari M., and M. Sukeri M. Yusof. "N-Benzoyl-N′-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 59, no. 2 (2003): o151—o152. http://dx.doi.org/10.1107/s1600536802023711.

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46

Zhang, You-Ming, Tai-Bao Wei, Liang Xian, Qi Lin, and Kai-Bei Yu. "N-Ethoxycarbonyl-N′-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): o905—o906. http://dx.doi.org/10.1107/s1600536803011607.

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47

Su, Hou-xiang. "1-Methyl-3-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 70, no. 5 (2014): o528. http://dx.doi.org/10.1107/s1600536814007442.

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The title compound, C8H10N2S, was prepared by reaction of methylamine solution, KOH and phenyl-isothiocyanate in ethanol. It adopts asyn-Me andanti-Ph conformation relative to the C=S double bond. The dihedral angle between the N—C(=S)—N thiourea and phenyl planes is 67.83 (6)°. In the crystal, the molecules centrosymmetrical dimers by pairs of N(Ph)—H...S hydrogen bonds. The dimers are linked by N(Me)—H...S hydrogen bonds into layers parallel to (100).

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48

Ramnathan, A., K. Sivakumar, K. Subramanian, N. Srinivasan, K. Ramadas, and H. K. Fun. "1-Cyclohexyl-3-phenylthiourea." Acta Crystallographica Section C Crystal Structure Communications 52, no. 3 (1996): 656–58. http://dx.doi.org/10.1107/s0108270195014065.

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49

Shahwar, Durre, M. Nawaz Tahir, Muhammad Mansha Chohan, Naeem Ahmad, and Samiullah. "3-Acetyl-1-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (2012): o508. http://dx.doi.org/10.1107/s1600536812002371.

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50

Defonsi Lestard, María Eliana, Diego M. Gil, Osvaldo Estévez-Hernández, Mauricio F. Erben, and Julio Duque. "Structural, vibrational and electronic characterization of 1-benzyl-3-furoyl-1-phenylthiourea: an experimental and theoretical study." New Journal of Chemistry 39, no. 9 (2015): 7459–71. http://dx.doi.org/10.1039/c5nj01210d.

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